Yayınlar & Eserler

Yayın Ağı
Makaleler 222
Tümü (222)
SCI-E, SSCI, AHCI (184)
SCI-E, SSCI, AHCI, ESCI (201)
ESCI (14)
Scopus (192)
TRDizin (36)
Diğer Yayınlar (11)

1. A novel loss of function mutation in the HAVCR2 gene in a patient diagnosed with Hodgkin’s lymphoma

Erdem S., YILMAZ E., ÖZCAN A., Canatan A. N., Bisgin A., Dogan M. E., et al.
Immunologic Research , cilt.73, sa.1, 2025 (SCI-Expanded, Scopus) identifier identifier identifier

2. Human plasma-derived plasminogen replacement in type 1 plasminogen deficiency: a pediatric case with multisystemic manifestation.

Göl D. K., Gök V., Yilmaz E., Ünal E., Karakükcü M., Celkan T. T., et al.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis , cilt.36, sa.8, ss.386-388, 2025 (SCI-Expanded, Scopus) identifier

3. A novel F7 mutation (p.Gly217Arg) associated with infantile intracranial hemorrhage successfully managed with rFVIIa.

Ozay M., Gumus U., Ünal E.
Thrombosis research , cilt.256, ss.109526, 2025 (SCI-Expanded, Scopus) identifier

4. Genetic and clinical characterization of factor VII deficiency: insights from 34 Turkish patients

Atik T., Ozen B. D., Isik E., Durmusalioglu E. A., Sarper N., Albayrak C., et al.
BLOOD COAGULATION & FIBRINOLYSIS , cilt.36, sa.7, ss.303-308, 2025 (SCI-Expanded, Scopus) identifier identifier identifier

5. Mast Cells Are Intrinsically Primed for Degranulation in DOCK8 Deficiency

Samanas N. B., Miralda I., Camp N., Sachen J., Puryear V., Shah L., et al.
Allergy: European Journal of Allergy and Clinical Immunology , cilt.80, sa.9, ss.2650-2653, 2025 (SCI-Expanded, Scopus) identifier identifier identifier identifier

6. A Rare Intersection: Wilms Tumor in a Patient with PIGO Syndrome

Akyol S., VURAL Ö., KAYHAN G., TÜRKYILMAZ Z., ÖZCAN A., Gol D. K., et al.
PEDIATRIC BLOOD & CANCER , cilt.72, sa.7, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

7. The phenomenological examination of Turkish mothers who have hemophilic sons

GÖK V., AYDOS S., Kıryar B. F., ÖZCAN A., YILMAZ E., KARAKÜKCÜ M., et al.
Trends in Pediatrics , cilt.6, sa.2, ss.95-101, 2025 (Scopus, TRDizin) Sürdürülebilir Kalkınma identifier identifier identifier

8. Clinical and laboratory aspects of patients diagnosed with various inherited platelet disorders

GÖK V., ÖZCAN A., Mutlu F. T., YILMAZ E., KOÇAK GÖL D., Ozay M., et al.
Research and Practice in Thrombosis and Haemostasis , cilt.9, sa.4, 2025 (SCI-Expanded, Scopus) identifier

9. Rituximab in pediatric B-cell Non-Hodgkin Lymphoma: Clinical outcomes and prognostic implications

AKYOL Ş., GÜZEL T., ÖZCAN A., Karaman S., Orhan M. F., Üzel V. H., et al.
Trends in Pediatrics , cilt.6, sa.1, ss.54-61, 2025 (Scopus, TRDizin) identifier

10. Clinical spectrum of primary hemophagocytic lymphohistiocytosis: experience of reference centers in Central and Southeast Anatolia

Akyol Ş., Yılmaz E., Tokgöz H., Karaman K., Pekpak E., Özcan A., et al.
ANNALS OF HEMATOLOGY , cilt.104, sa.1, ss.123-130, 2025 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

11. Successful Treatment of Childhood Hodgkin Lymphoma and Secondary Myelofibrosis Resistant to Intensive Therapy, Including Allogeneic Transplantation

GÖL D. K., gök v., Ozcan A., YILMAZ E., UNAL E., Abdulrezzak Ü., et al.
TURKISH JOURNAL OF HEMATOLOGY , cilt.42, sa.2, ss.158-160, 2025 (SCI-Expanded, Scopus, TRDizin) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier identifier

12. DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans

Azizoglu Z. B., Babayeva R., Haskologlu Z. S., Acar M. B., Ayaz-Guner S., Okus F. Z., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.44, sa.8, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

13. Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis

Chiang S. C. C., Covill L. E., Tesi B., Campbell T. M., Schlums H., Nejati-Zendegani J., et al.
Blood , cilt.144, sa.8, ss.873-887, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

14. Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants

GÖK V., LEBLEBİSATAN G., Gokcebay D. G., GÜLER S., Dogan M. E., Bozdogan S. T., et al.
BRITISH JOURNAL OF HAEMATOLOGY , cilt.205, sa.1, ss.236-242, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

15. Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis

IŞIK E., AYDINOK Y., Albayrak C., Durmus B., Karakas Z., Orhan M. F., et al.
EUROPEAN JOURNAL OF HAEMATOLOGY , cilt.113, sa.1, ss.82-89, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

16. 30 Years of Wilms Tumor Experience at One Center in Türkiye's Central Anatolia Region

AKYOL Ş., ODABAŞ G. P., ÖZCAN A., YILMAZ E., KARAMAN Z. F., ÖZTÜRK F., et al.
JOURNAL OF CHILD - COCUK DERGISI , cilt.23, sa.4, ss.344-348, 2024 (ESCI, TRDizin) identifier identifier

17. Rare Coagulation Factor Deficiencies: Multicenter Experience With 188 Cases

GÖK V., Sahinoglu E. P., Tokgoz H., Mutlu F. T., Acipayam C., Karaman K., et al.
JOURNAL OF CHILD - COCUK DERGISI , cilt.23, sa.4, ss.349-355, 2024 (ESCI, TRDizin) identifier identifier

18. Alantolactone ameliorates graft versus host disease in mice

Odabas G. P., Aslan K., Suna P. A., Kendirli P. K., Erdem Ş., Çakır M., et al.
INTERNATIONAL IMMUNOPHARMACOLOGY , cilt.128, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

19. Repetitive intra-articular therapy in fungal arthritis: Adjunct to systemic therapy in a patient with pediatric acute lymphoblastic leukemia

AKYOL Ş., Erdoğmuş N. A., ATALAY M. A., KARAMAN Z. F., ÖZCAN A., KAFADAR İ. H., et al.
Trends in Pediatrics , cilt.5, sa.3, ss.101-104, 2024 (Scopus, TRDizin) identifier identifier

20. The Effect of Nivolumab in Pediatric Malignant Tumors: A Single Center Experience with Nine Children

GÖK V., Aydin F., ÖZCAN A., KARAMAN Z. F., DÜNDAR YENİLMEZ E., Gorukmez O., et al.
UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , cilt.34, sa.4, ss.184-194, 2024 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier

21. Neurological Complications in Children With Cancer: Experience From a Single Center in Türkiye

Kara L., Unal E., PER H., Kumandas S., CANPOLAT M., Elmali F., et al.
JOURNAL OF CLINICAL PRACTICE AND RESEARCH , cilt.46, sa.2, ss.154-160, 2024 (ESCI, TRDizin) Sürdürülebilir Kalkınma identifier identifier

22. A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature

Lanz A., Erdem S., ÖZCAN A., CEYLANER G., CANSEVER M., CEYLANER S., et al.
Journal of Clinical Immunology , cilt.44, sa.1, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

23. JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study

Fischer M., Olbrich P., Hadjadj J., Aumann V., Bakhtiar S., Barlogis V., et al.
Journal of Allergy and Clinical Immunology , cilt.153, sa.1, ss.275, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

24. A case of autoimmune lymphoproliferative syndrome with a novel de novo FAS variant

Özçelik F., Aslan K., Gök V., Ari M. B., Özcan A., Eken A., et al.
Pediatric Hematology and Oncology , cilt.41, sa.4, ss.301-309, 2024 (SCI-Expanded, Scopus) identifier identifier identifier

25. Treatment of Infantile Fibrosarcoma in the Era of Targeted Therapies

Yildirim U. M., Kebudi R., Asarcikli F., Sozmen B. O. F. L. A. Z., ÜNAL E., ÖZCAN A., et al.
UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , cilt.33, sa.4, ss.240-247, 2023 (SCI-Expanded, Scopus, TRDizin) identifier identifier

26. C-terminal variants in CDC42 drive type I interferon-dependent autoinflammation in NOCARH syndrome reversible by ruxolitinib

Kapp F. G., Kretschmer S., Beckmann C. C., Wäsch L., Molitor A., Carapito R., et al.
CLINICAL IMMUNOLOGY , cilt.256, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

27. Aceruloplasminemia presenting with microcytic anemia in a Turkish boy due to a novel pathogenic variant

Gok V., Ozcan A., Ozer S., Karaman F., Aykutlu E., Yilmaz E., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.40, sa.7, ss.673-681, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

28. Changes in Mucosa-Associated Invariant T Cells (Mait), Assocıated Cytokines, and MR-1+ Cell Number And Phenotype In The Peripheral Blood of Pediatric ITP Patients with and without Eltrombopag Therapy

Eken A., Çil M., Azizoglu Z. B., Üzen R., Asaad N. N., Calık S., et al.
Hematology, Transfusion and Cell Therapy , cilt.45, ss.17-18, 2023 (ESCI, Scopus) Sürdürülebilir Kalkınma

29. Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1

Erdem S., Haskoloğlu Z. Ş., Haliloglu Y., Celikzencir H., Arik E., Keskin O., et al.
Clinical Immunology , cilt.253, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

30. Dedicator of cytokinesis 8 (DOCK8) is a negative regulator of skin mast cell function

Molina I. M., Samanas N. B., Seo A. J., Foronda J., Deutsch G. H., BARIŞ S., et al.
JOURNAL OF IMMUNOLOGY , cilt.210, sa.1, 2023 (SCI-Expanded, Scopus) Creative Commons License identifier

31. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.

Leiding J. W., Vogel T. P., Santarlas V. G. J., Mhaskar R., Smith M. R., Carisey A., et al.
The Journal of allergy and clinical immunology , cilt.151, sa.4, ss.1081-1095, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

32. The influence of RANKL/osteoprotegerin on the prognosis of childhood acute lymphoblastic leukemia

AKYOL Ş., ÖZCAN A., YILMAZ E., PATIROĞLU T., ÖZDEMİR M. A., ÜNAL E.
MediHealth Academy , cilt.2, sa.1, ss.17-20, 2023 (Hakemli Dergi)

33. Inherited Bone Marrow Failure Syndromes in Children

Ertunç M. E., Çelik A. G., Tahiroglu A., ÜNAL E.
The journal of pediatric academy (Online) , cilt.4, sa.1, ss.1-5, 2023 (TRDizin) Creative Commons License identifier

34. T-cell/histiocyte-rich large B-cell lymphoma in a patient with a novel frameshift MSH6 mutation

ÇEKİÇ Ş., AYDIN F., Karali Y., SEVİNİR B. B., CANÖZ Ö., Boztug K., et al.
PEDIATRIC BLOOD & CANCER , cilt.70, sa.3, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

35. Hypomorphic RAG deficiency: impact of disease burden on survival and thymic recovery argues for early diagnosis and HSCT

Schuetz C., Gerke J., Ege M., Walter J., Kusters M., Worth A., et al.
Blood , cilt.141, sa.7, ss.713-724, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

36. Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.

Linder M. I., Mizoguchi Y., Hesse S., Csaba G., Tatematsu M., Łyszkiewicz M., et al.
Blood , cilt.141, sa.6, ss.645-658, 2023 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

37. Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency

Levy R., Gothe F., Momenilandi M., Magg T., Materna M., Peters P., et al.
JOURNAL OF EXPERIMENTAL MEDICINE , cilt.220, sa.2, 2023 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

38. Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment

Gök V., Erdem Ş., Haliloğlu Y., Bişgin A., Belkaya S., Başaran K. E., et al.
GENES AND IMMUNITY , cilt.24, sa.1, ss.12-20, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

39. Haploidentical Antibody Response against Vaccine Antigens in Children after TCRab-Depleted Haploidentical Stem Cell Transplantation: Is It Similar to That in Recipients with Fully Matched Donors?

KONDOLOT M., YILMAZ E., Sahin N. E., ÖZCAN A., KAYNAR L., ÜNAL E., et al.
TRANSPLANTATION AND CELLULAR THERAPY , cilt.29, sa.2, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier

40. Antibody Response against Vaccine Antigens in Children after TCRαβ-Depleted Haploidentical Stem Cell Transplantation: Is It Similar to That in Recipients with Fully Matched Donors?

Kondolot M., Yilmaz E., Sahin N. E., Ozcan A., Kaynar L., Unal E., et al.
Transplantation and cellular therapy , cilt.29, sa.2, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

41. A Fatal Case of Familial Hemophagocytic Lymphohistiocytosis Associated with Fusarium Infection and Rare Mutation

DÜNDAR M. A., ORAK F., ACIPAYAM C., Aslan K., Gök V., ÇETİN B. Ş., et al.
ERCIYES MEDICAL JOURNAL , cilt.45, sa.2, ss.207-210, 2023 (ESCI, TRDizin) Sürdürülebilir Kalkınma identifier identifier

42. Wilms Tumor Experience of 30 years in the Single Center, Central Anatolia Region of Turkey

AKYOL Ş., ODABAŞI G. P., ÖZCAN A., YILMAZ E., KARAMAN Z. F., ÖZTÜRK F., et al.
Çocuk Dergisi , 2023 (TRDizin)

43. Assessment of extracorporeal photopheresis related cell damage.

Samur B. M., KARAKÜKCÜ Ç., ÖZCAN A., ÜNAL E., YILMAZ E., KARAKÜKCÜ M.
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis , cilt.61, sa.6, ss.103472, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

44. Intracranial hemorrhage in children with hemophilia

Akyol Ş., Göl D. K., Yılmaz E., Karaman Z. F., Özcan A., Küçük A., et al.
J Transl Pract Med , cilt.1, sa.3, ss.85-88, 2022 (Hakemli Dergi)

45. A pilot study for treatment of severe COVID-19 pneumonia by aerosolized formulation of convalescent human immune plasma exosomes (ChipEXO™)

GÜL F., GÖNEN Z. B., Jones O. Y., Taşlı N. P., ZARARSIZ G., ÜNAL E., et al.
FRONTIERS IN IMMUNOLOGY , cilt.13, 2022 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

46. Central Nervous System Fungal Infections in Children With Leukemia and Undergoing Hematopoietic Stem Cell Transplantation: A Retrospective Multicenter Study

Karaman S., Kebudi R., Kizilocak H., Karakas Z., Demirag B., SEZGİN EVİM M., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.44, sa.8, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

47. Evaluation of primary care physicians' approaches to hemophilia and bleeding disorders: a questionnaire survey

Samur B. M., Samur T. G., Çiflikli F., Özcan A., Gök V., Soykan R., et al.
BLOOD COAGULATION & FIBRINOLYSIS , cilt.33, sa.7, ss.381-388, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

48. The Significance of soluble CD40 and CD40 ligand levels in childhood acute lymphoblastic leukemia patients

Gök V., Özcan A., Yılmaz E., Karakükcü M., Patıroğlu T., Özdemir M. A., et al.
Journal of Translational and Practical Medicine , cilt.1, sa.2, ss.49-56, 2022 (Hakemli Dergi) Creative Commons License

49. Triosephosphate isomerase deficiency in an infant

Karaca M., Gök V., Sarı Ü. A., Dündar M. A., Aydın F., Özcan A., et al.
Journal of Translational and Practical Medicine , cilt.1, sa.2, ss.65-67, 2022 (Hakemli Dergi) Creative Commons License

50. Characterization of cord blood CD3+TCRVα7.2+CD161high T and innate lymphoid cells in the pregnancies with gestational diabetes, morbidly adherent placenta, and pregnancy hypertension diseases

Haliloglu Y., Ozcan A., Erdem S., Azizoglu Z. B., Bicer A., Ozarslan Ö. Y., et al.
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY , cilt.88, sa.1, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

51. Comprehensive approach to hemophilia

Gök V., Ünal E.
JOURNAL OF HEALTH SCIENCES AND MEDICINE , cilt.5, sa.4, ss.1199-1206, 2022 (TRDizin) Creative Commons License

52. A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman-Diamond syndrome

Alsavaf M. B., Verboon J. M., DOĞAN M. E., Azizoglu Z. B., Okus F. Z., ÖZCAN A., et al.
BRITISH JOURNAL OF HAEMATOLOGY , cilt.197, sa.6, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

53. The Mutation of CD27 Deficiency Presented With Familial Hodgkin Lymphoma and a Review of the Literature

Kose D., GÜZELÇİÇEK A., Oz O., Erdem A. Y., Haliloglu Y., Witzel M., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.44, sa.4, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

54. Social exclusion and behavior problems in adolescents with cancer and healthy counterparts

SEZER EFE Y., ÖZBEY H., CANER N., ERDEM E., Kuzucu E. G., KARAKÜKCÜ M., et al.
JOURNAL OF PEDIATRIC NURSING-NURSING CARE OF CHILDREN & FAMILIES , cilt.64, 2022 (SCI-Expanded, SSCI, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

55. Molecular spectrum of Von Willebrand Disease Type 3

IŞIK E., AYYILDIZ EMECEN D., Kavakli K., ŞAHİN F., Durmusalioglu E. A., ALBAYRAK C., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.30, sa.SUPPL 1, ss.227-228, 2022 (SCI-Expanded, Scopus) identifier

56. A teenager boy with a novel variant of Sitosterolemia presented with pancytopenia.

Gok V., Tada H., Ensar Dogan M., ALAKUŞ SARI Ü., ASLAN K., ÖZCAN A., et al.
Clinica chimica acta; international journal of clinical chemistry , cilt.529, ss.61-66, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

57. Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency

Kocamış B., Baser D., Akcam B., Danielson J., Eltan S. B., Haliloglu Y., et al.
ALLERGY , cilt.77, sa.3, ss.1004-1019, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

58. Therapeutic effects of vitamin D and IL-22 on methotrexate-induced mucositis in mice

YILMAZ E., Azizoglu Z. B., Aslan K., Erdem S., Haliloglu Y., Suna P. A., et al.
ANTI-CANCER DRUGS , cilt.33, sa.1, ss.11-18, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

59. A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia.

Goktas S., Azizoglu Z. B., Petersheim D., Erdogan M., Eke Gungor H., Bisgin A., et al.
Journal of pediatric hematology/oncology , cilt.44, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

60. A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia

GÖKTAŞ S., Azizoglu Z. B., Petersheim D., ERDOĞAN M., Eke Gungor H., Bisgin A., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.44, sa.1, 2022 (SCI-Expanded, Scopus) identifier identifier identifier

61. Etiological Factors of Opsoclonus Myoclonus Ataxia Syndrome: A Single Center Experience with Eight Children

Gök V., Gümüş G., Durmuş H., Ünal E., Gümüş H., Karakükcü M., et al.
TRENDS IN PEDIATRICS , cilt.3, sa.4, ss.120-125, 2022 (ESCI, TRDizin) identifier identifier

62. A NOVEL MISSENSE MUTATION OUTSIDE DNAJ DOMAIN OF DNAJC21 IS ASSOCIATED WITH SHWACHMAN-DIAMOND SYNDROME

Alsavaf M. B., Verboon J. M., Dogan M. E., Azizoglu Z. B., Okus F. Z., Ozcan A., et al.
Hematology, Transfusion and Cell Therapy , cilt.43, sa.3, ss.61-62, 2021 (Scopus)

63. Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous Candidiasis

Frede N., Rojas-Restrepo J., Caballero Garcia de Oteyza A., Buchta M., Huebscher K., Gamez-Diaz L., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.8, ss.1804-1838, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

64. Immunomagnetic separation of B type acute lymphoblastic leukemia cells from bone marrow with flow cytometry validation and microfluidic chip measurements

İçöz K., Eken A., Cinar S., Murat A., Özcan S., Ünal E., et al.
SEPARATION SCIENCE AND TECHNOLOGY , cilt.56, sa.15, ss.2659-2666, 2021 (SCI-Expanded, Scopus) identifier identifier

65. Single-center experience of childhood Hodgkin lymphoma treated without radiotherapy

YILMAZ E., ARSLAN M., AKYOL Ş., ÖZCAN A., ZARARSIZ G., ABDÜLREZZAK Ü., et al.
Journal of Health Sciences and Medicine , cilt.4, sa.6, ss.853-857, 2021 (TRDizin) identifier

66. Long-Term Follow-Up of Patients with a Diagnosis of Posterior Reversible Encephalopathy Syndrome

CANPOLAT M., Ozcora G. D. K., Poyrazoglu H., PER H., Coskun A., GÜMÜŞ H., et al.
TURKISH ARCHIVES OF PEDIATRICS , cilt.56, sa.6, ss.569-575, 2021 (ESCI, Scopus, TRDizin) Sürdürülebilir Kalkınma identifier identifier identifier

67. Blood repellent superhydrophobic surfaces constructed from nanoparticle-free and biocompatible materials

ÇELİK N., Sahin F., Ruzi M., Yay M., ÜNAL E., ÖNSES M. S.
COLLOIDS AND SURFACES B-BIOINTERFACES , cilt.205, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

68. The spectrum of underlying diseases in children with autoimmune hemolytic anemia

ÖZCAN A., CANSEVER M., YILMAZ E., ÜNAL E., KARAKÜKCÜ M., PATIROĞLU T.
Journal of Health Sciences and Medicine , cilt.4, sa.6, ss.772-778, 2021 (TRDizin) identifier

69. Transplantation for ultra high-risk neuroblastoma patients: Effect of tandem autologous stem cell transplantation

YILMAZ E., SAMUR M. B., ÖZCAN A., ÜNAL E., KARAKÜKCÜ M.
Journal of Health Sciences and Medicine , cilt.4, sa.6, ss.943-948, 2021 (TRDizin) identifier

70. Characterization of Th17 and Treg cells in leucocyte adhesion deficiency 1 patients

Erdem S., Haliloglu Y., Haskaloglu S., Arik E., KESKİN Ö., Karadag S. I. K., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.298, 2021 (SCI-Expanded, Scopus) identifier

71. A nonsense mutation in DIAPH1 gene presents with major T cell defects

Azizoglu Z. B., Okus F. Z., ÖZCAN A., Sawaf B., KÖSE M., CANÖZ Ö., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.296, 2021 (SCI-Expanded, Scopus) identifier

72. The number and activity of CD3(+)TCR V alpha 7.2(+)CD161(+) cells are increased in children with acute rheumatic fever

Ozkaya M., Baykan A., Cakir M., Vural C., Sunkak S., Unal E., et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY , cilt.333, ss.174-183, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

73. Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia

Casini A., von Mackensen S., Santoro C., Khayat C. D., Belhani M., Ross C., et al.
BLOOD , cilt.137, sa.22, ss.3127-3136, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

74. Type 1 Plasminogen Deficiency With Pulmonary Involvement: Novel Treatment and Novel Mutation

HANGÜL M., TÜZÜNER A. B., Somekh I., Klein C., PATIROĞLU T., ÜNAL E., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.43, sa.4, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

75. Refractory and Fatal Presentation of Severe Autoimmune Hemolytic Anemia in a Child With the DNASE1L3 Mutation Complicated With an Additional DOCK8 Variant.

Paç K., Witzel M., Unal E., Rohlfs M., Akyildiz B., Dogan M. E., et al.
Journal of pediatric hematology/oncology , cilt.43, sa.3, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

76. Comprehensive Mutation Analysis of the RAS/RAF/MEK/ERK Pathway in Paediatric Leukaemia and Significant Inferences

Akin-Bali D. F., AKTAŞ S. H., ÖZCAN A., YILMAZ E., AYDIN F., GÖK V., et al.
HONG KONG JOURNAL OF PAEDIATRICS , cilt.26, sa.2, ss.75-87, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier

77. Common Variable Immunodeficiency, Autoimmune Hemolytic Anemia, and Pancytopenia Associated With a Defect in IKAROS

Yilmaz E., Kuehn H., Odakir E., Niemela J., Ozcan A., Eken A., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , sa.3, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

78. Two pediatric cases of gastric adenocarcinoma and review of the literature

Altay D., Karaman Z. F., Özcan A., Deniz K., Ünal E., Patiroğlu T., et al.
Erciyes Medical Journal , cilt.43, sa.3, ss.296-299, 2021 (ESCI, TRDizin) identifier identifier

79. Type 2B Von Willebrand Disease Mimicking Autoimmune Thrombocytopenia in the Neonatal Period

GÖK V., IŞIK E., YILMAZ E., AYDIN F., ÖZCAN A., ÜNAL E., et al.
ERCIYES MEDICAL JOURNAL , cilt.43, sa.2, ss.201-203, 2021 (ESCI, TRDizin) identifier identifier

80. Effect of vitamin K2 and vitamin D3 on bone mineral density in children with acute lymphoblastic leukemia: a prospective cohort study.

SOLMAZ I., ÖZDEMİR M. A., ÜNAL E., Abdurrezzak Ü., Muhtaroglu S., KARAKÜKCÜ M.
Journal of pediatric endocrinology & metabolism : JPEM , cilt.34, sa.4, ss.441-447, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

81. Long-Term Patient-Customized Therapy for a Pathogenic EPO Mutation

Ejaz A., ÖZCAN A., ÜNAL E., KARAKÜKCÜ M., Sankaran V. G.
MED , cilt.2, sa.1, ss.33-38, 2021 (ESCI, Scopus) Creative Commons License identifier identifier identifier

82. Expanded circulating hematopoietic stem/progenitor cells as novel cell source or the treatment of TCIRG1 osteopetrosis

Capo V., Penna S., Merelli I., Barcella M., Scala S., Basso-Ricci L., et al.
HAEMATOLOGICA , cilt.106, sa.1, ss.74-86, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

83. The Spectrum of Underlying Diseases in Children with Torticollis

Tumturk A., Gorkem S. B., Ozmansur E. N., Peduk Y., Arslan U., Gok V., et al.
TURKISH NEUROSURGERY , sa.3, ss.389-398, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

84. Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

ÖZEN A. O., ÖZEN A. O., Edwards E. S. J., Pillay B., ÖZEN A. O., ÖZEN A. O., et al.
BLOOD , cilt.136, sa.23, ss.2638-2655, 2020 (SCI-Expanded, Scopus) identifier identifier identifier

85. Hepatitis-associated aplastic anemia in pediatric patients: single center experience.

Altay D., Yılmaz E., Özcan A., Karakükçü M., Ünal E., Arslan D.
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis , cilt.59, 2020 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

86. Inflammatory Myofibroblastic Tumor of the Bronchus Mimicking Asthma

HANGÜL M., ÖNAL Ö., ÖZCAN A., ÜNAL E., KÖSE M.
Journal of Pediatric Academy , cilt.1, sa.3, ss.103-104, 2020 (Hakemli Dergi)

87. Different Clinical Presentation of 3 Children With Familial Hemophagocytic Lymphohistiocytosis With 2 Novel Mutations

Akyol S., Ozcan A., Sekine T., Chiang S., Yilmaz E., Karakurkcu M., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.42, sa.7, 2020 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

88. Microfluidic Chip based direct triple antibody immunoassay for monitoring patient comparative response to leukemia treatment

İÇÖZ K., Akar U., ÜNAL E.
BIOMEDICAL MICRODEVICES , cilt.22, sa.3, 2020 (SCI-Expanded, Scopus) identifier identifier identifier

89. Impact of Intrauterine Growth Restriction Diseases on The Umbilical Cord Blood CD34 Cell Counts

Türkoglu E. M., Erdem S., Bicer A., Okus F. Z., ÖZCAN A., azizoglu z. B., et al.
Journal of Pediatric Academy , ss.51-56, 2020 (Hakemli Dergi)

90. Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community

Simon A. J., Golan A. C., Lev A., Stauber T., Barel O., Somekh I., et al.
CLINICAL IMMUNOLOGY , cilt.214, 2020 (SCI-Expanded, Scopus) identifier identifier identifier

91. Role of a second transplantation for children with acute leukemia following posttransplantation relapse: a study by the Turkish Bone Marrow Transplantation Study Group

Hazar V., Karasu G. T., Uygun V., Ozbek N., KARAKÜKCÜ M., Ozturk G., et al.
LEUKEMIA & LYMPHOMA , cilt.61, sa.6, ss.1465-1474, 2020 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

92. ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients

Eken A., Cansever M., Okus F. Z., Erdem S., Nain E., Azizoglu Z. B., et al.
ALLERGY , cilt.75, sa.4, ss.921-933, 2020 (SCI-Expanded, Scopus) identifier identifier identifier

93. Congenital afibrinogenemia in a 4-year-old girl complicated with acute lymphoblastic leukemia

ÖZCAN A., Samur B., AKYOL Ş., Erdogmus N. A., PATIROĞLU T., KARAKÜKCÜ M., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.62, sa.2, ss.289-292, 2020 (SCI-Expanded, Scopus, TRDizin) identifier identifier identifier

94. Twenty children with non-Wilms renal tumors from a reference center in Central Anatolia, Turkey

Ünal E., Yilmaz E., Özcan A., Işik B., Karakükcü M., Turan C., et al.
Turkish journal of medical sciences , cilt.50, ss.18-24, 2020 (SCI-Expanded, Scopus, TRDizin) identifier identifier identifier

95. Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

Lyszkiewicz M., Zietara N., Frey L., Pannicke U., Stern M., Liu Y., et al.
NATURE COMMUNICATIONS , cilt.11, sa.1, 2020 (SCI-Expanded, Scopus) identifier identifier identifier

96. Assesment of Patients with Von Willebrand Disease with ISTH/BAT and PBQ Scores

Belen A., Ümit E., Zengin Y., Sezgin E., Ünal E., Özbaş H., et al.
Turkish journal of haematology : official journal of Turkish Society of Haematology , cilt.37, ss.57-58, 2020 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier

97. Glioblastoma and Colorectal Adenocarcinoma in anAdolescent Girl with Constitutional Mismatch RepairDeficiency syndrome mimicking Neurofibromatosis Type-I

Aydın F., Altay D., Görükmez O., Kiraz Hafo A., Karaman Z. F., Özcan A., et al.
The Journal of Pediatric Academy , cilt.1, sa.1, ss.34-38, 2020 (Hakemli Dergi)

98. Gliomatosis Cerebri Mimicking Encephalopathy in a Teenager Boy

Isik B., Gumus U., ÖZCAN A., YILMAZ E., Mutlu F. T., CANÖZ Ö., et al.
GAZI MEDICAL JOURNAL , cilt.31, ss.726-728, 2020 (ESCI, Scopus) identifier identifier

99. Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease

Ravell J., Matsuda-Lennikov M., Chauvin S., Zou J., Biancalana M., Deeb S., et al.
JOURNAL OF CLINICAL INVESTIGATION , cilt.130, sa.1, ss.507-522, 2020 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

100. Vena cava superior syndrome in the children with mediastinal tumors: Single-center experience

ÖZCAN A., ÜNAL E., KARAKÜKCÜ M., COŞKUN A., ÖZDEMİR M. A., PATIROĞLU T.
NORTHERN CLINICS OF ISTANBUL , cilt.7, sa.3, ss.255-259, 2020 (ESCI, TRDizin) identifier identifier

101. Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations

ATİK T., IŞIK E., Onay H., Akgun B., Shamsali M., Kavaklo K., et al.
TURKISH JOURNAL OF HEMATOLOGY , cilt.37, sa.3, ss.145-153, 2020 (SCI-Expanded, Scopus, TRDizin) identifier identifier identifier

102. Invasive Fungal Infections in Children with Acute Lymphoblastic Leukemia: Experience from a Reference University Hospital in Cappadocia

YILMAZ E., Erdogmus A., ÖZCAN A., GÖRKEM S. B., Ceylan O., DENİZ K., et al.
UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , cilt.30, sa.3, ss.126-132, 2020 (SCI-Expanded, Scopus, TRDizin) Sürdürülebilir Kalkınma identifier identifier

103. A rare cause of vomiting in an adolescent: gastric Burkitt`s lymphoma.

Altay D., Özcan A., Ünal E., Deniz K., Özkan K. U., Patıroğlu T., et al.
Turkish Journal Of Pediatrics , cilt.61, sa.3, ss.431-435, 2019 (SCI-Expanded, Scopus, TRDizin)

104. CARMIL2 Deficiency Presenting as Very Early Onset Inflammatory Bowel Disease

Magg T., Shcherbina A., Arslan D., Desai M., Wall S., Mitsialis V., et al.
INFLAMMATORY BOWEL DISEASES , cilt.25, sa.11, ss.1788-1795, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

105. CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis

Somekh I., Thian M., Medgyesi D., Gülez N., Magg T., Gallón D., et al.
BLOOD , cilt.134, sa.18, ss.1510-1516, 2019 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

106. Burkitt Leukemia in a 5-Year-Old Girl with Williams-Beuren Syndrome: Review of the Literature

PATIROĞLU T., ÖZCAN A., KARAKÜKCÜ M., Ozdemir M. A., ÜNAL E.
INDIAN JOURNAL OF MEDICAL AND PAEDIATRIC ONCOLOGY , cilt.40, 2019 (ESCI, Scopus) identifier identifier

107. Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency

Farmer J., Foldvari Z., Ujhazi B., De R., Chen K., Bleesing J., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE , cilt.7, sa.6, ss.1970-1989, 2019 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

108. Successful Rapid Desensitization of Two Teenagers with Rituximab Hypersensitivity

CANSEVER M., ÖZCAN A., DURSUN I., ÜNAL E., TAHAN F.
JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH , cilt.13, sa.5, 2019 (ESCI) identifier

109. Genetic Deficiency and Biochemical Inhibition of ITK Affect Human Th17, Treg, and Innate Lymphoid Cells

Eken A., Cansever M., Somekh I., Mizoguchi Y., Zietara N., Okus F., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.39, sa.4, ss.391-400, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

110. A rare cause of vomiting in an adolescent: gastric Burkitt's lymphoma

ALTAY D., ÖZCAN A., ÜNAL E., DENİZ K., ÖZKAN K. U., PATIROĞLU T., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.61, sa.3, ss.431-435, 2019 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier

111. Propranolol treatment for chylothorax due to diffuse lymphangiomatosis

HANGÜL M., KÖSE M., ÖZCAN A., ÜNAL E.
PEDIATRIC BLOOD & CANCER , cilt.66, sa.5, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

112. Hepatosplenic Fungal Infections in Children With Leukemia-Risk Factors and Outcome: A Multicentric Study

Celkan T., Kizilocak H., Evim M., Meral G., Özbek N., Yarali N., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.41, sa.4, ss.256-260, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

113. A Rare Case of Activated Phosphoinositide 3-Kinase Delta Syndrome (APDS) Presenting With Hemophagocytosis Complicated With Hodgkin Lymphoma.

Cansever M., Zietara N., Chiang S., Ozcan A., Yilmaz E., Karakukcu M., et al.
Journal of pediatric hematology/oncology , 2019 (SCI-Expanded, Scopus) identifier identifier identifier

114. A mummy emerges from the grave: Scurvy confounding the clinical presentation of a child with Fanconi anemia

Ozcan A., Saracoglu S., Verboon J., Karakukcu M., Patiroglu T., Coskun A., et al.
AMERICAN JOURNAL OF HEMATOLOGY , cilt.94, sa.4, ss.506-507, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

115. Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition

Grabowski P., Hesse S., Hollizeck S., Rohlfs M., Behrends U., Sherkat R., et al.
MOLECULAR & CELLULAR PROTEOMICS , cilt.18, sa.4, ss.760-772, 2019 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

116. Capturing B type acute lymphoblastic leukemia cells using two types of antibodies

İÇÖZ K., Gercek T., Murat A., ÖZCAN S., ÜNAL E.
BIOTECHNOLOGY PROGRESS , cilt.35, sa.1, 2019 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

117. Biliary Rhabdomyosarcoma in an Infant Male With Neurofibromatosis Type 1

Alhashem F., Yilmaz E., Özdemir M. M., Deniz K., Yikilmaz A., Patıroğlu T., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.41, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

118. Scurvy: A rare cause of arthritis in a child with neurologic disorder.

KÜÇÜKAYDıN Z., Dursun İ., DALDABAN B., ÖZCAN A., ÜNAL E.
European journal of rheumatology , cilt.5, ss.283-284, 2018 (SCI-Expanded, TRDizin) Creative Commons License identifier identifier

119. Central Nervous System Fungal Infections in Children with Leukemia: Risk Factors and Outcome: A Multicentric Study

Karaman S., Kebudi R., Kizilocak H., Karakas Z., Evim M. S., Kaya Z., et al.
PEDIATRIC BLOOD & CANCER , cilt.65, 2018 (SCI-Expanded, Scopus) identifier

120. Vena Cava Superior Syndrome in Children with Mediastinal Tumors: Single Center Experience

PATIROĞLU T., ÖZCAN A., ÜNAL E., KARAKÜKCÜ M., COŞKUN A.
PEDIATRIC BLOOD & CANCER , cilt.65, 2018 (SCI-Expanded, Scopus) identifier

121. Tumour Lysis Syndrome in Children with Hematologic Malignancies: Single Center Experience

PATIROĞLU T., ÖZCAN A., ÜNAL E., KARAKÜKCÜ M., TURAN C.
Pediatric Blood & Cancer , cilt.65, ss.27455, 2018 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

122. DOES EVEN LOW DOSE ENALAPRIL CAUSE LIFE THREATENING ACUTE KIDNEY INJURY?

GÜNAY N., DURSUN I., ÜNAL E., ÖZCAN A., PINARBAŞI A. S., ÖZKAYA M., et al.
PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1842, 2018 (SCI-Expanded, Scopus) identifier

123. Evaluation of childhood solid pseudopapillary tumors of the pancreas.

Ozcan A., Arslanoglu C., Unal E., Patiroglu T., Ozdemir M., Deniz K., et al.
Northern clinics of Istanbul , cilt.5, ss.207-210, 2018 (Hakemli Dergi) Creative Commons License identifier identifier

124. Cerebral Sinus Venous Thrombosis and Prothrombotic Risk Factors in Children: A Single-Center Experience From Turkey

ÖZCAN A., CANPOLAT M., Doganay S., ÜNAL E., KARAKÜKCÜ M., ÖZDEMİR M., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.40, sa.6, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

125. Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma

Somekh I., Marquardt B., Liu Y., Rohlfs M., Hollizeck S., KARAKÜKCÜ M., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.38, sa.6, ss.699-710, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

126. Quartz-crystal Microbalance Measurements of CD19 Antibody Immobilization on Gold Surface and Capturing B Lymphoblast Cells: Effect of Surface Functionalization

İçöz K., Soylu M. Ç., Canıkara Z., Ünal E.
ELECTROANALYSIS , cilt.30, ss.834-841, 2018 (SCI-Expanded, Scopus) identifier identifier

127. Group 3 innate lymphoid cells are absent in DOCK8- defective HIES patients

EKEN A., okuş f. z., PATIROĞLU T., erdem ş., KARAKÜKCÜ M., CANSEVER M., et al.
The journal of İmmunology , 2018 (SCI-Expanded, Scopus)

128. ALLOGENEIC BONE MARROW TRANSPLANTATION IN THREE CASES WITH DOCK 8 DEFICIENCY

PATIROĞLU T., CANSEVER M., ÖZCAN A., Ucan G., Keles S., ÜNAL E., et al.
HLA , cilt.91, sa.5, ss.388, 2018 (SCI-Expanded, Scopus) identifier

129. The relationship between hematological parameters and prognosis of children with acute ischemic stroke

Yilmaz E., Kacar A. B., Bozpolat A., ZARARSIZ G., GÖRKEM B., KARAKÜKCÜ M., et al.
CHILDS NERVOUS SYSTEM , cilt.34, sa.4, ss.655-661, 2018 (SCI-Expanded, Scopus) identifier

130. Pansitopeni ile başvuran metilmalonik asidemi: Olgu sunumu

BAŞTUĞ O., ÖZTÜRK M. A., KORKMAZ L., MEMUR Ş., HALİS H., KARDAŞ F., et al.
Bakirkoy Tip Dergisi / Medical Journal of Bakirkoy , cilt.14, sa.1, ss.138-41, 2018 (Scopus, TRDizin)

131. A case of congenital fibrinogen deficiency complicated with acute lymphoblastic leukemia

ÖZCAN A., SAMUR M. B., ERDOĞMUŞ A., PATIROĞLU T., KARAKÜKCÜ M., ÜNAL E.
Haemophilia , cilt.24, ss.32-135, 2018 (SCI-Expanded, Scopus) Creative Commons License identifier

132. Pleural Effusion in a 17-Year-Old-Male with ChronicMiyeloid Leukemia due to the use of Imatinib

PATIROĞLU T., ÖZCAN A., köse s., ÜNAL E., KARAKÜKCÜ M., COŞKUN A.
Annals of Hematology Oncology , cilt.5, ss.1191, 2018 (Hakemli Dergi)

133. Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five Patients

TÜFEKÇİ Ö., KOÇAK Ü., KAYA Z., Yenicesu I., Albayrak C., Albayrak D., et al.
TURKISH JOURNAL OF HEMATOLOGY , cilt.35, sa.1, ss.27-34, 2018 (SCI-Expanded, Scopus, TRDizin) identifier identifier identifier

134. Effectiveness of Ankaferd BloodStopper in Prophylaxis and Treatment of Oral Mucositis in Childhood Cancers Evaluated with Plasma Citrulline Levels

Patiroglu T., Sahin N. E., Unal E., Kendirci M., KARAKÜKCÜ M., Ozdemir M. A.
TURKISH JOURNAL OF HEMATOLOGY , cilt.35, sa.1, ss.85-86, 2018 (SCI-Expanded, Scopus, TRDizin) Sürdürülebilir Kalkınma identifier identifier identifier

135. Hepatosplenic Fungal Infections in Children with Leukemia, Risk Factors and Outcome: A Multicentric Study

Kizilocak H., Kebudi R., Dikme G., Ucar A. K., Ozbek N. Y., ÜNAL E., et al.
PEDIATRIC BLOOD & CANCER , cilt.64, 2017 (SCI-Expanded, Scopus) identifier

136. A Case of Familial Hemophagocytic Lymphohistiocytosis Type 4 With Involvement of the Central Nervous System Complicated With Infarct

Ciraci S., ÖZCAN A., ÖZDEMİR M., Chiang S. C. C., Tesi B., ÖZDEMİR A. T., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.39, sa.6, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

137. A Newborn With Familial Hemophagocytic Lymphohistiocytosis Complicated With Transfusion Associated Graft Versus Host Disease

Ozdemir A., GÜNEŞ T., CHIANG S. C. C., ÜNAL E.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.39, sa.6, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

138. Apparent diffusion coefficient in differentiation of pediatric posterior fossa tumors

Zitouni S., Koc G., Doganay S., SARAÇOĞLU S., GUMUS K. Z., Ciraci S., et al.
JAPANESE JOURNAL OF RADIOLOGY , cilt.35, sa.8, ss.448-453, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

139. Hematopoietic Stem Cell Transplant for Primary Immunodeficiency Diseases A Single Center Experience

PATIROĞLU T., AKAR H., ÜNAL E., ÖZDEMİR M. A., KARAKÜKCÜ M.
Experimental And Clinical Transplantation , cilt.15, sa.3, ss.337-343, 2017 (SCI-Expanded, Scopus)

140. Neuroblastoma in a Child With Wolf-Hirschhorn Syndrome

ÖZCAN A., Acer H., Ciraci S., GÜMÜŞ H., KARAKÜKCÜ M., PATIROĞLU T., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.39, sa.4, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

141. Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation

Kim A. R., Ulirsch J. C., WİLMES S., ÜNAL E., Moraga I., KARAKÜKCÜ M., et al.
CELL , cilt.168, sa.6, ss.1053-1079, 2017 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

142. Utility of the aspergillus galactomannan antigen testing for neutropenic paediatric patients

Sav H., ATALAY M. A., KOÇ A. N., ÜNAL E., Demir G., ZARARSIZ G.
Infezioni in Medicina , cilt.25, sa.1, ss.38-44, 2017 (Scopus) Sürdürülebilir Kalkınma identifier identifier

143. Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency

Levy R., Okada S., Beziat V., Moriya K., Liu C., Chai L. Y. A., et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , cilt.113, sa.51, 2016 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

144. Fibromuscular Dysplasia Complicated With Cerebral Stroke in a Child With Congenital Dyserythropoietic Anemia Type II

ÖZCAN A., PATIROĞLU T., Acer H., GÜMÜŞ H., Senol S., KARAKÜKCÜ M., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.38, sa.8, 2016 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

145. Diffusion weighted imaging in differentiating malignant and benign neuroblastic tumors

SERIN H., GORKEM S. B., DOGANAY S., CıRACı S., UNAL E., GUZEL M., et al.
JAPANESE JOURNAL OF RADIOLOGY , cilt.34, sa.9, ss.620-624, 2016 (SCI-Expanded, Scopus) identifier identifier identifier

146. Severe Combined Immunodeficiencies Resulting from Impaired Purine Metabolism Single Center Experience

PATIROĞLU T., AKARSU H., GÜNGOR H. E., ÜNAL E., ınes s., hersfield m., et al.
Asthma Allergy Immunology , cilt.14, sa.1, ss.18-23, 2016 (TRDizin)

147. THE ROLE OF HLA TYPING TO DIAGNOSE MATERNAL ENGRAFTMENT SYNDROME IN PATIENTS WITH SEVERE COMBINED IMMUNE DEFICIENCY

PATIROĞLU T., Bektas F., ÖZCAN A., ÜNAL E.
HLA , cilt.87, sa.4, ss.305, 2016 (SCI-Expanded, Scopus) identifier

148. Leukemia Cutis Mimicking Kerion Celsi A challenging Diagnosis for Clinicians

KARTAL D., ÇINAR L. S., GÜL KIRKAŞ Ö., ÜNAL E., CANÖZ Ö., BORLU M.
Clinical Pediatric Dermatology , cilt.2, sa.1, ss.1-3, 2016 (Hakemli Dergi)

149. Familial moyamoya disease in two Turkish siblings with same polymorphism in RNF213 gene but different clinical features.

Bayram A., Yilmaz E., Per H., Ito M., Uchino H., Doganay S., et al.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery , cilt.32, ss.569-73, 2016 (SCI-Expanded, Scopus) identifier identifier identifier

150. Prognostic Factors and a New Prognostic Index Model for Children and Adolescents with Hodgkin's Lymphoma Who Underwent Autologous Hematopoietic Stem Cell Transplantation: A Multicenter Study of the Turkish Pediatric Bone Marrow Transplantation Study Group

Kesik V., Atas E., KARAKÜKCÜ M., AKSOYLAR S., Erbey F., TAÇYILDIZ N., et al.
TURKISH JOURNAL OF HEMATOLOGY , cilt.33, sa.4, ss.265-272, 2016 (SCI-Expanded, Scopus, TRDizin) Sürdürülebilir Kalkınma identifier identifier identifier

151. Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis

TESI B., LAGERSTEDT-ROBINSON K., CHIANG S. C. C., BEN BDIRA E., ABBOUD M., Belen B., et al.
GENOME MEDICINE , cilt.7, 2015 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

152. EFFECTIVENESS OF ANKAFERD BLOOD STOPPER IN PROPHYLAXIS AND TREATMENT OF ORAL MUCOSITIS SEEN IN CHILDHOOD CANCERS AND CORRELATION WITH PLASMA CITRULLINE LEVELS

PATIROĞLU T., ŞAHİN N., ÜNAL E., KENDİRCİ M., ÖZDEMİR M. M., KARAKÜKCÜ M.
PEDIATRIC BLOOD & CANCER , cilt.62, 2015 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier

153. Torticollis in children: an alert symptom not to be turned away

TÜMTÜRK A., OZCORA G. K., BAYRAM A. K., Kabaklioglu M., Doganay S., CANPOLAT M., et al.
CHILDS NERVOUS SYSTEM , cilt.31, sa.9, ss.1461-1470, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

154. AUTOSOMAL RECESSIVE HYPER IgM SYNDROME ASSOCIATED WITH ACTIVATION-INDUCED CYTIDINE DEAMINASE GENE IN THREE TURKISH SIBLINGS PRESENTED WITH TUBERCULOSIS LYMPHADENITIS - CASE REPORT

PATIROĞLU T., AKAR H. H., VAN DER BURG M., ÜNAL E.
ACTA MICROBIOLOGICA ET IMMUNOLOGICA HUNGARICA , cilt.62, sa.3, ss.267-274, 2015 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

155. Inflammatory Myofibroblastic Tumor of the Kidney and Bilateral Lung Nodules in a Child Mimicking Wilms Tumor With Lung Metastases

DOĞAN M., Doganay S., Koc G., GÖRKEM S. B., ÜNAL E., ÖZTÜRK F., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.37, sa.6, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

156. Stem cell mobilization and collection from pediatric patients and healthy children

KARAKÜKCÜ M., ÜNAL E.
TRANSFUSION AND APHERESIS SCIENCE , cilt.53, sa.1, ss.17-22, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

157. A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease

PATIROĞLU T., AKAR H. H., Gilmour K., ÜNAL E., ÖZDEMİR M., BIBI S., et al.
CLINICAL IMMUNOLOGY , cilt.159, sa.1, ss.58-62, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

158. A case of congenital afibrinogenemia complicated with thromboembolic events that required repeated amputations

ÖZDEMİR M., Isik B., PATIROĞLU T., KARAKÜKCÜ M., MUTLU F. T., Yilmaz E., et al.
BLOOD COAGULATION & FIBRINOLYSIS , cilt.26, sa.3, ss.354-356, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

159. Malignancies in Primary Immunodeficiencies: A Single Center Experience

PATIROĞLU T., AKAR H. H., ÜNAL E., ÖZDEMİR M., KARAKÜKCÜ M., PATIROĞLU T.
PEDIATRIC ALLERGY IMMUNOLOGY AND PULMONOLOGY , cilt.28, sa.1, ss.47-54, 2015 (SCI-Expanded, Scopus) identifier identifier

160. Brain Abscesses in Children: Results of 24 Children From a Reference Center in Central Anatolia, Turkey

CANPOLAT M., Ceylan O., PER H., Koc G., TÜMTÜRK A., KUMANDAŞ S., et al.
JOURNAL OF CHILD NEUROLOGY , cilt.30, sa.4, ss.458-467, 2015 (SCI-Expanded, Scopus) identifier identifier identifier

161. The Importance of Nucleated Red Blood Cells in Patients with Beta Thalassemia Major and Comparison of Two Automated Systems with Manual Microscopy and Flow Cytometry

KARAKÜKCÜ M., Karakukcu C., ÜNAL E., ÖZTÜRK A., cıracı Z., PATIROĞLU T., et al.
CLINICAL LABORATORY , cilt.61, sa.9, ss.1289-1295, 2015 (SCI-Expanded, Scopus) identifier identifier

162. Fetal intracranial hemorrhage related to maternal autoimmune thrombocytopenic purpura

Kutuk M. S., CROISILLE L., GÖRKEM S. B., Yilmaz E., Korkmaz L., BIERLING P., et al.
CHILDS NERVOUS SYSTEM , cilt.30, sa.12, ss.2147-2150, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

163. Acute Colchicine Intoxication Complicated With Extramedullary Hematopoiesis Due to Filgrastim in a Child

Kilic S. C., Alaygut D., ÜNAL E., Koc E., PATIROĞLU T.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.36, sa.7, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

164. Atypical Severe Combined Immunodeficiency Caused by a Novel Homozygous Mutation In Rag1 Gene in a Girl who Presented with Pyoderma Gangrenosum: A Case Report and Literature Review

PATIROĞLU T., AKAR H. H., Gilmour K., ÖZDEMİR M., Bibi S., Henriquez F., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.34, sa.7, ss.792-795, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

165. Cranial metastatic alveolar rhabdomyosarcoma mimicking hematological malignancy in an adolescent boy

PATIROĞLU T., Isik B., ÜNAL E., CANÖZ Ö., DENİZ K., KÖSEMEHMETOĞLU K., et al.
CHILDS NERVOUS SYSTEM , cilt.30, sa.10, ss.1737-1741, 2014 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

166. Intracranial hemorrhage in infants as a serious, and preventable consequence of late form of vitamin K deficiency: a selfie picture of Turkey, strategies for tomorrow

ÜNAL E., ÖZSOYLU S., Bayram A., Ozdemir M. A., Yilmaz E., CANPOLAT M., et al.
CHILDS NERVOUS SYSTEM , cilt.30, sa.8, ss.1375-1382, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

167. Inherited biallelic CSF3R mutations in severe congenital neutropenia

TRIOT A., JAERVINEN P. M., Arostegui J. I., MURUGAN D., KOHISTANI N., Dapena Díaz J. L., et al.
BLOOD , cilt.123, sa.24, ss.3811-3817, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

168. Childhood Stroke: Results of 130 Children From a Reference Center in Central Anatolia, Turkey

PER H., ÜNAL E., Poyrazoglu H. G., Ozdemir M. A., DÖNMEZ H., GÜMÜŞ H., et al.
PEDIATRIC NEUROLOGY , cilt.50, sa.6, ss.595-600, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

169. Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels

SASSİ A., LAZAROSKİ S., WU G., HASLAM S. M., FLIEGAUF M., MELLOULI F., et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.133, sa.5, ss.1410-1432, 2014 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

170. Neurological complication of non Hodgkin lymphoma in childhood: experience from a single center in Turkey

Kose D., Paksoy Y., Koksal Y., ÜNAL E.
CHILDS NERVOUS SYSTEM , cilt.30, sa.4, ss.639-645, 2014 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

171. Oral and Dental Findings of the Longest Surviving Patient with Hoyeraal-Hreidarsson Syndrome

ŞEKERCİ A. E., Keskinrüzgar A., ŞİŞMAN Y., ÜNAL E., KARAKÜKCÜ M., ÖZDEMİR M. A.
Journal of Oral Health and Community Dentistry , cilt.1, sa.8, ss.65-69, 2014 (Hakemli Dergi)

172. Is there relation between COL4A1/A2 mutations and antenatally detected fetal intraventricular hemorrhage?

Kutuk M. S., Balta B., Kodera H., Matsumoto N., Saitsu H., Doganay S., et al.
CHILDS NERVOUS SYSTEM , cilt.30, sa.3, ss.419-424, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

173. Rapamycin has a beneficial effect on controlling epilepsy in children with tuberous sclerosis complex: results of 7 children from a cohort of 86

CANPOLAT M., PER H., GÜMÜŞ H., Yikilmaz A., ÜNAL E., PATIROĞLU T., et al.
CHILDS NERVOUS SYSTEM , cilt.30, sa.2, ss.227-240, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

174. Gastric Signet Ring Carcinoma in a Patient With Ataxia-Telangiectasia: A Case Report and Review of the Literature

PATIROĞLU T., Gungor H. E., ARSLAN D., DENİZ K., ÜNAL E., COŞKUN A.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.35, sa.8, 2013 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

175. The Efficacy of Vitamin K-2 and Calcitriol Combination on Thalassemic Osteopathy

ÖZDEMİR M. M., Yilmaz K., ABDÜLREZZAK Ü., Muhtaroglu S., PATIROĞLU T., KARAKÜKCÜ M., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.35, sa.8, ss.623-627, 2013 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

176. GLIOMATOSIS CEREBRI MIMICKING ENCEPHALITIS: A CASE REPORT

ÖZDEMİR M. M., Mutlu F., PER H., Isik B., ÜNAL E., YILMAZ E.
PEDIATRIC BLOOD & CANCER , cilt.60, ss.241, 2013 (SCI-Expanded, Scopus) identifier

177. PULMONARY LANGERHANS CELL HISTIOCYTOSIS MIMICKING BRONCHIAL ASTHMA

Ozdemir M., KÖSE M., CANÖZ Ö., HASDIRAZ L., ÜNAL E., Mutlu F.
PEDIATRIC BLOOD & CANCER , cilt.60, ss.242, 2013 (SCI-Expanded, Scopus) identifier

178. Infantile tremor syndrome associated with cobalamin therapy: A case report

PATIROĞLU T., ÜNAL E., Yildirim S.
CLINICAL NEUROLOGY AND NEUROSURGERY , cilt.115, sa.9, ss.1903-1905, 2013 (SCI-Expanded, Scopus) identifier identifier identifier

179. CHRONIC GRANULOMATOUS DISEASE WITH MARKEDLY ELEVATED IGE LEVELS MIMICKING HYPERIMMUNOGLOBULIN E SYNDROME A CASE REPORT

PATIROĞLU T., Gungor H. E., Lazaroski S., ÜNAL E.
ACTA MICROBIOLOGICA ET IMMUNOLOGICA HUNGARICA , cilt.60, sa.2, ss.155-162, 2013 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

180. THE CLINICAL FEATURES AND GENETIC MUTATIONS OF CHRONIC GRANULOMATOUS DISEASE: RESULTS FROM A REFERENCE CENTRE AT MIDDLE ANATOLIA

Patiroglu T., Gungor H., ÜNAL E., KÖKER M. Y.
HAEMATOLOGICA , cilt.98, ss.732, 2013 (SCI-Expanded, Scopus) identifier

181. THE CLINICAL FEATURES AND GENETIC MUTATIONS OF CHRONIC GRANULOMATOUS DISEASE: RESULTS FROM A REFERENCE CENTRE AT MIDDLE ANATOLIA

PATIROĞLU T., GUNGOR H. E., ÜNAL E., KOKER Y.
GENETIC COUNSELING , cilt.24, sa.3, ss.327-335, 2013 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

182. Multiple Fungal Brain Abscesses in a Child with Acute Lymphoblastic Leukemia

PATIROĞLU T., ÜNAL E., KARAKÜKCÜ M., Ozdemir M. A., Tucer B., Yikilmaz A., et al.
MYCOPATHOLOGIA , cilt.174, ss.505-509, 2012 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

183. Cerebellar hemangioblastoma associated with diffuse neonatal hemangiomatosis in an infant

PATIROĞLU T., SARICI D., ÜNAL E., Yikilmaz A., Tucer B., KARAKÜKCÜ M., et al.
CHILDS NERVOUS SYSTEM , cilt.28, sa.10, ss.1801-1805, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

184. The Importance of Bronchoalveolar Lavage Sample for Galactomannan, 1,3-beta-D-Glucan and PCR Tests

Sav H., Atalay M. A., ÜNAL E., Koc N.
MIKROBIYOLOJI BULTENI , cilt.46, sa.4, ss.695-701, 2012 (SCI-Expanded, Scopus, TRDizin) identifier

185. AUTOIMMUNE DISEASES DETECTED IN CHILDREN WITH PRIMARY IMMUNODEFICIENCY DISEASES: RESULTS FROM A REFERENCE CENTRE AT MIDDLE ANATOLIA

PATIROĞLU T., Gungor H. E., ÜNAL E.
ACTA MICROBIOLOGICA ET IMMUNOLOGICA HUNGARICA , cilt.59, sa.3, ss.343-353, 2012 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

186. The efficacy of Pelargonium sidoides in the treatment of upper respiratory tract infections in children with transient hypogammaglobulinemia of infancy

PATIROĞLU T., Tunc A., Gungor H. E., ÜNAL E.
PHYTOMEDICINE , cilt.19, sa.11, ss.958-961, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

187. Hemophagocytic syndrome in a 4-month-old infant with biotinidase deficiency

KARDAŞ F., PATIROĞLU T., ÜNAL E., Chiang S. C. C., Bryceson Y. T., KENDİRCİ M.
PEDIATRIC BLOOD & CANCER , cilt.59, sa.1, ss.191-193, 2012 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

188. Hemophagocytic syndrome in a 4-month-old infant with biotinidase

KARDAŞ F., PATIROĞLU T., ÜNAL E., Chiang S. C., Bryceson Y. T., KENDİRCİ M.
Pediatr Blood Cancer.. , cilt.15, ss.191-193, 2012 (SCI-Expanded)

189. Accidental intramuscular overdose administration of vincristine

PATIROĞLU T., ÜNAL E., Ozdemir M. A., Karakukucu M., Mutlu F. T.
DRUG AND CHEMICAL TOXICOLOGY , cilt.35, sa.2, ss.232-234, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

190. Orbital myositis associated with focal active colitis in a teenage girl

Kondolot M., ÜNAL E., Poyrazoglu G., Kara A., Yikilmaz A., KUMANDAŞ S., et al.
CHILDS NERVOUS SYSTEM , cilt.28, sa.4, ss.641-643, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

191. Hashimoto thyroiditis associated with ataxia telangiectasia

Patıroğlu T., Güngör H. E., Ünal E., Kurtoglu S., Yıkılmaz A., Patıroğlu T.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.25, ss.349-352, 2012 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier

192. Ataxia telangiectasia and secondary diseases

PATIROĞLU T., GUNGOR H. E., Baz H., Unal E.
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.47, sa.1, ss.38-42, 2012 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier

193. Atrial fibrillation as an uncommon presentation in a large pleomorphic xanthoastrocytoma

Sezer S., BAYKAN A., Yılmaz E., Ünal E., Onan S. H., Yıkılmaz A., et al.
CHILDS NERVOUS SYSTEM , cilt.28, sa.3, ss.475-479, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

194. Late-type vitamin K deficiency bleeding: experience from 120 patients

Ozdemir M. A., KARAKÜKCÜ M., PER H., ÜNAL E., GÜMÜŞ H., PATIROĞLU T.
CHILDS NERVOUS SYSTEM , cilt.28, sa.2, ss.247-251, 2012 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

195. The importance of MTHFR polymorphisms in pediatric cerebral stroke

ÜNAL E., Mutlu F. T., KARAKÜKCÜ M.
CHILDS NERVOUS SYSTEM , cilt.28, sa.1, ss.13, 2012 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

196. COENZYME Q(10) LEVELS IN beta-THALASSEMIA AND ITS ASSOCIATION WITH FERRITIN LEVELS AND CHELATION THERAPY

Karakukcu C., KARAKÜKCÜ M., ÜNAL E., PATIROĞLU T., ÖZDEMİR M., Torun Y. A., et al.
HEMOGLOBIN , cilt.36, sa.3, ss.219-229, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

197. Intracranial hemorrhage in children with congenital factor deficiencies

PATIROĞLU T., Ozdemir M. A., ÜNAL E., Torun Y. A., COŞKUN A., Menku A., et al.
CHILDS NERVOUS SYSTEM , cilt.27, sa.11, ss.1963-1966, 2011 (SCI-Expanded, Scopus) identifier identifier identifier

198. Web-based survey of resources for treatment and long-term follow-up for children with brain tumors in developing countries

Qaddoumi I., ÜNAL E., Diez B., Kebudi R., Quintana Y., Bouffet E., et al.
CHILDS NERVOUS SYSTEM , cilt.27, sa.11, ss.1957-1961, 2011 (SCI-Expanded, Scopus) identifier identifier identifier

199. Phenylketonuria With Acute Myeloblastic Leukemia in a 9-year-old Boy: Reporting a Rare Case

PATIROĞLU T., ÜNAL E., KARDAŞ F., Ozdemir M. A., KARAKÜKCÜ M., Sayilmaz O.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.33, sa.6, 2011 (SCI-Expanded, Scopus) identifier identifier identifier

200. Mycophenolate mofetil-induced pseudotumor cerebri in a boy with autoimmune lymphoproliferative disease

PATIROĞLU T., Ozcan A., KARAKÜKCÜ M., Ozdemir M. A., Poyrazoglu G., CANPOLAT M., et al.
CHILDS NERVOUS SYSTEM , cilt.27, sa.5, ss.853-855, 2011 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

201. Reply from the authors of the article entitled "Atypical presentation of chronic granulomatous disease in an adolescent boy with frontal lobe located Aspergillus abscess mimicking intracranial tumor"

ÜNAL E., Yikilmaz A., PATIROĞLU T.
CHILDS NERVOUS SYSTEM , cilt.26, sa.6, ss.735, 2010 (SCI-Expanded, Scopus) Creative Commons License identifier identifier

202. Release of N-terminal pro-brain natriuretic peptide in children with acute rheumatic carditis

ÇİMEN Ö., ORAN B., ÇİMEN D., BAYSAL T., Karaaslan S., Unal E., et al.
CARDIOLOGY IN THE YOUNG , cilt.20, sa.3, ss.297-301, 2010 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

203. Neuroblastoma Arising From an Unresected Sacrococcygeal Teratoma in a Child

ÜNAL E., KÖKSAL Y., TOY H., GÜNEL E., AÇIKGÖZOGLU S.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.32, sa.3, ss.233-235, 2010 (SCI-Expanded, Scopus) identifier identifier

204. Atypical presentation of chronic granulomatous disease in an adolescent boy with frontal lobe located Aspergillus abscess mimicking intracranial tumor

PATIROĞLU T., ÜNAL E., Yikilmaz A., Koker M. Y., ÖZTÜRK M.
CHILDS NERVOUS SYSTEM , cilt.26, sa.2, ss.149-154, 2010 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

205. CARDIAC FUNCTIONS EVALUATED WITH TISSUE DOPPLER IMAGING IN CHILDHOOD CANCERS TREATED WITH ANTHRACYCLINES

BAYSAL T., Köksal Y., ORAN B., SEN M., ÜNAL E., ÇİMEN D.
PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.27, sa.1, ss.13-23, 2010 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

206. The Importance of Cystatin-C for Predicting Nephrotoxicity in Children with Acute Leukemia and Non-Hodgkin Lymphoma

Unal E., Caliskan U., Koksal Y.
UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , cilt.19, sa.2, ss.69-74, 2009 (SCI-Expanded, Scopus, TRDizin) Sürdürülebilir Kalkınma identifier identifier

207. Merkel Cell Carcinoma in a Child

KÖKSAL Y., Toy H., TALİM B., Unal E., AKÇÖREN Z., CENGİZ M.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.31, sa.5, ss.359-361, 2009 (SCI-Expanded, Scopus) identifier identifier identifier

208. Hypothermia in a Child With Hodgkin Disease

Koksal Y., Caliskan U., Unal E.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.31, sa.2, ss.136-138, 2009 (SCI-Expanded, Scopus) identifier identifier identifier

209. Malignant glioblastomatous transformation of a low-grade glioma in a child

ÜNAL E., KÖKSAL Y., ÇİMEN Ö., PAKSOY Y., TAVLI L.
CHILDS NERVOUS SYSTEM , cilt.24, sa.12, ss.1385-1389, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

210. Cerebral venous sinus thrombosis in an adolescent with Ewing sarcoma

ÜNAL E., YAZAR A., KÖKSAL Y., ÇALIŞKAN Ü., PAKSOY Y., KALKAN E.
CHILDS NERVOUS SYSTEM , cilt.24, sa.9, ss.983-986, 2008 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

211. Importance of chemoprophylaxis and vaccines in the prevention of recurrent meningitis

Unal E., Koksal Y., Energin V. M., Reisli I.
PEDIATRICS INTERNATIONAL , cilt.50, sa.3, ss.416, 2008 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

212. The importance of chemoprophylaxis and vaccines in the prevention of recurrent meningitis

ÜNAL E., KOKSAL Y., ENERGİN M., REİSLİ İ.
PEDIATRICS INTERNATIONAL , cilt.50, 2008 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

213. Pilocytic astrocytoma developing at the site of a previously treated medulloblastoma in a child

KOKSAL Y., TOY H., ÜNAL E., BAYSAL T., ESEN H., PAKSOY Y., et al.
CHILDS NERVOUS SYSTEM , cilt.24, sa.3, ss.289-292, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

214. Astroblastoma in a child

Unal E., Koksal Y., Vajtai I., Toy H., Kocaogullar Y., Paksoy Y.
CHILDS NERVOUS SYSTEM , cilt.24, sa.2, ss.165-168, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

215. Childs Nerv Syst

ÜNAL E., KOKSAL Y., VAJTAI I., Toy H., KOCAOGULLAR Y., PAKSOY Y.
Astroblastoma in a child , cilt.24, ss.166-168, 2008 (SCI-Expanded)

216. Thyroid medullary carcinoma in a teenager with Cowden syndrome

KOKSAL Y., SAHIN M., KOKSAL H., ORHAN D., ÜNAL E., ALAGÖZ E.
LARYNGOSCOPE , cilt.117, sa.7, ss.1180-1182, 2007 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

217. Fatal valproate overdose in a newborn baby

ÜNAL E., Kaya Ü., AYDIN K.
HUMAN & EXPERIMENTAL TOXICOLOGY , cilt.26, sa.5, ss.453-456, 2007 (SCI-Expanded, Scopus) identifier identifier identifier

218. Pituitary-adrenal axis suppression due to topical steroid administration in an infant

Atabek M. E., Pirgon O., Unal E.
PEDIATRICS INTERNATIONAL , cilt.49, sa.2, ss.242-244, 2007 (SCI-Expanded, Scopus) identifier identifier identifier

219. Kluver-Bucy syndrome in a boy with non-Hodgkin lymphoma

ÜNAL E., KOKSAL Y., BAYSAL T., ENERGIN M., AYDIN K., ÇALIŞKAN Ü.
PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.24, sa.2, ss.149-152, 2007 (SCI-Expanded, Scopus) identifier identifier identifier

220. Pulmonary arterial pressure in infants with laryngomalacia

ÜNAL E., ORAN B., Baysal T., BAŞPINAR O., Keser M., Karaarslan S., et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , cilt.70, sa.12, ss.2067-2071, 2006 (SCI-Expanded, Scopus) identifier identifier identifier

221. The real incidence of thyroid carcinoma in childhood

ÜNAL E.
LARYNGOSCOPE , cilt.116, 2006 (SCI-Expanded, Scopus)

222. Refractory cutaneous leishmaniasis in an adolescent: initial manifestation of type 1 diabetes

PIRGON O., ATABEK E., ÜNAL E.
J Infect , cilt.53, ss.290-291, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 127

1. Graft Versus Host Hastalığı tedavisinde Schisandrin-B’nin etkisinin araştırılması

Aslan K., Odabaşı G. P., Alişan Suna P., Yay A. H., Özcan A., Yılmaz E., et al.
49.Ulusal Hematoloji Kongresi, Antalya, Türkiye, 2 - 05 Kasım 2023, ss.1, (Özet Bildiri)

2. Anti-biofouling, blood-repellent and biocompatible coatings for medical equipment interfaces

Sahin F., ÇELİK N., ÜNAL E., SEZER G., CEYLAN A., ÖNSES M. S.
2022 Medical Technologies Congress, TIPTEKNO 2022, Antalya, Türkiye, 31 Ekim - 02 Kasım 2022, (Tam Metin Bildiri) Sürdürülebilir Kalkınma identifier identifier

3. Novel variant detected in the FAS gene of a patient with Autoimmune Lymphoproliferative Syndrome

ARI M. B., YAMAN T., ÇALIŞKAN Ç., ÖZÇELİK F., ÖZCAN A., ÖZKUL Y., et al.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.56, (Özet Bildiri)

4. Nanopartikül İçermeyen Biyouyumlu Malzemelerle Yapılmış Kan İtici Süperhidrofobik Yüzeyler

ÇELİK N., ŞAHİN F., Ruzi M., YAY M., ÜNAL E., ÖNSES M. S.
XIV ULUSAL KAN MERKEZLERİ VE TRANSFÜZYON TIBBI KONGRESİ, Antalya, Türkiye, 03 Kasım 2021, (Tam Metin Bildiri)

5. Refrakter Nöroblastom Hastalarında Tandem Yüksek Doz MIBG ve Otolog Hematopoetik Kök Hücre Nakli

YILMAZ E., SAMUR M. B., ÖZCAN A., GÖK V., AYDIN F., ÜNAL E., et al.
13. Ulusal Kemik İliği Transplantasyonu ve Hücresel Tedaviler Kongresi, Türkiye, 2 - 03 Nisan 2021, ss.108, (Özet Bildiri)

6. Ekstrakorporeal Fotoferez İlişkili DNA Hasarlarının Araştırılması

SAMUR M. B., KARAKÜKCÜ Ç., YILMAZ E., ÖZCAN A., KEKLİK M., GÖK V., et al.
13. Ulusal Kemik İliği Transplantasyonu ve Hücresel Tedaviler Kongresi, Türkiye, 2 - 03 Nisan 2021, ss.102-103, (Özet Bildiri)

7. HEMOPHILIA INTERNATIONAL ACCREDITATION TRAINING PLAN IN ERCIYES UNIVERSITY PEDIATRIC HEMATOLOGY CLINIC

GÖK V., GÜL KUZUCU E., ATASEVEN L., CÜCE İ., DOĞAN M. E., ABDÜLREZZAK Ü., et al.
HAEMOPHILIA, 10 Şubat 2021, cilt.27, ss.29-30, (Özet Bildiri)

8. Hemophilia International Accreditation Training Plan in Erciyes University Pediatric Hematology Clinic

GÖK V., KUZUCU E. G., ATASEVEN L., CÜCE İ., DOĞAN M. E., ABDÜLREZZAK Ü., et al.
Virtual Congress of the European Association for Haemophilia and Allied Disorders, 3 - 05 Şubat 2021, cilt.27, ss.29-30, (Özet Bildiri)

9. A PERSISTENT MONOARTHRITIS AND CLINICAL DETERIORATION IN A PATIENT RECEIVING TNF INHIBITOR THERAPY FOR JUVENILE IDIOPATHIC ARTHRITIS

ÇETİN B. Ş., PAÇ KISAARSLAN A., ÜNAL E., HANGÜL M., KÖSE M.
38th Annual Meeting of the European Society for Paediatric Infectious Diseases (ESPID 2020), 26 - 29 Ekim 2020, (Özet Bildiri)

10. AN INFANT WITH NOVEL MUTATION OF ALDOLASE A DEFICIENCY PRESENTED WITH NEUROMETABOLIC SIGNS AND BASOPHILIC STRIPPING ON PERIPHERAL BLOOD SMEAR

ÖZCAN A., KADIOĞLU YILMAZ B., ÜNAL E., KARDAŞ F., ELKATMIŞ T., KUMANDAŞ S.
EHA 2020, 11 - 13 Haziran 2020, (Özet Bildiri)

11. SEIZURE AS A RARE SIDE EFFECT OF L-ASPARAGINASE INFUSION IN A LEUKEMIC CHILD WITH DOWN SYNDROME

GÖK V., AYDIN F., ÖZCAN A., YILMAZ E., ACER H., GÖRKEM S. B., et al.
EHA, 11 - 21 Haziran 2020, cilt.1, ss.1, (Özet Bildiri)

12. COMBINATION OF TWO RARE GENETIC DISEASES OF FANCONI APLASTIC ANEMIA AND 46,X,DEL(X)(Q23) IN A TURKISH GIRL

GÖK V., DOĞAN M. E., YILMAZ E., ÖZCAN A., TORUN Y., AYDIN F., et al.
EHA 2020, 11 - 13 Haziran 2020, (Özet Bildiri)

13. NAKİL HASTALARINDA GRANÜLOSİT SÜSPANSİYONUKULLANIMININ ENGRAFTMAN SÜRECİNE ETKİSİ

YILMAZ E., ÖZCAN A., KAYNAR L., ÜNAL E., PATIROĞLU T., KARAKÜKCÜ M.
12. Ulusal Kemik İliği Transplantasyonu ve Hücresel Tedaviler Kongresi, Türkiye, 5 - 07 Mart 2020, ss.71, (Tam Metin Bildiri)

14. Cafe Au Late Lekeleri ve Malignite Birlikteliği Nörofibromatozis Tip-1 mi DNA Yanlış Eşleşme Onarımı Sendromu mu?

AYDIN F., GÖRÜKMEZ O., GÖRKEM S. B., GÖK V., ÖZCAN A., YILMAZ E., et al.
6. Erciyes Pediatri Akademisi Kış Kongresi, Kayseri, Türkiye, 27 - 29 Şubat 2020, ss.195, (Özet Bildiri)

15. L- asparaginaz infüzyonu sırasında konvulziyon olur mu?

GÖK V., AYDIN F., ÖZCAN A., YILMAZ E., ACER H., Erdoğmuş N. A., et al.
6. Erciyes Pediatri Akademisi Kış Kongresi, Kayseri, Türkiye, 27 - 29 Şubat 2020, ss.192-193, (Özet Bildiri)

16. Afibrinogenemia Experience: Multicenter Study

TUNCEL D. A., GÖK V., PEKPAK E., TOKGÖZ H., ACIPAYAM C., YILMAZ E., et al.
13th Annual Congress of European Association for Hemophilia and Allied Disorders 2020, Hollanda, 5 - 07 Şubat 2020, (Özet Bildiri)

17. İmmun Yetmezlikte TcR αβ (+) Deplesyonu ile Haploidentik Hematopoietik Kök Hücre Nakli

YILMAZ E., ÖZCAN A., ÜNAL E., PATIROĞLU T., KARAKÜKCÜ M.
1. Uluslararası Rûmi Pediatri Kongresi, Konya, Türkiye, 4 - 07 Aralık 2019, ss.157-159, (Tam Metin Bildiri)

18. BİLATERAL AURİKULER KİTLEHİPERİMMÜNGLOBULİNE SENDROMU

VURAL A., NURSAÇAN C. O., KARA İ., KETENCİ İ., KARAKÜKCÜ M., PATIROĞLU T., et al.
39. Türk Ulusal Kulak Burun Boğaz ve Baş Boyun Cerrahisi Kongresi, Türkiye, 8 - 12 Kasım 2019, (Özet Bildiri)

19. AUTOIMMUNE HEMOLITIC ANEMIA (AIHA) IN CHILDHOOD IS PRIMARY IMMUNE DISORDERS MORE OFTEN THAN EXPECTED IN ETIOLOGY OF SECONDARY AIHA

PATIROĞLU T., ÖZCAN A., CANSEVER M., ÜNAL E., YILMAZ E., KARAKÜKCÜ M.
24th Congress of the European Hematology Association, Amsterdam, Hollanda, 13 - 16 Haziran 2019, ss.895, (Özet Bildiri)

20. A neglected enemy of hematopoietic stem cell transplant patients: tuberculosis

HANGÜL M., ÖZCAN A., KARAKÜKCÜ M., PATIROĞLU T., ÇETİN B. Ş., ÜNAL E., et al.
37th Annual Meeting of the European Society for Paediatric Infectious Diseases, ESPID 2019, Slovenya, 6 - 11 Mayıs 2019, (Özet Bildiri) Sürdürülebilir Kalkınma

21. Vena Cava Superior Syndrome in Children with Mediastinal Tumors: Single Center Experience

PATIROĞLU T., ÖZCAN A., ÜNAL E., KARAKÜKCÜ M.
international society of pediatric oncology, 16 - 19 Kasım 2018, (Tam Metin Bildiri)

22. CENTRAL NERVOUS SYSTEM FUNGAL INFECTIONS IN CHILDREN WITH LEUKEMIA:RISK FACTORS AND OUTCOME: A MULTICENTRIC STUDY

KARAMAN S., KEBUDİ R., KIZILOCAK H., KARAKAŞ Z., SEZGİN EVİM M., KAYA Z., et al.
50 TH SIOP, KYOTO, JAPON, PEDIATRIC BLOOD CANCERVolume: 65 Pages: S390-S390 Supplement: 2 Meeting Abstract: PO, 16 - 19 Kasım 2018, (Tam Metin Bildiri)

23. RELAPS AKUT LÖSEMİSİ OLAN PEDİATRİK OLGULARDAİKİNCİ HEMATOPOİETİK KÖK HÜCRE NAKİL SONUÇLARI

HAZAR V., KARASU G., UYGUN V., ÖZBEK N. Y., KARAKÜKCÜ M., ÖZTÜRK H. G., et al.
44.ULUSAL HEMATOLOJİ KONGRESİ, Türkiye, 31 Ekim - 03 Kasım 2018, ss.195, (Tam Metin Bildiri)

24. Emerging pathogen: Candida kefyr (Kluvyeromyces marxianus) in pediatric hematopoietic stem cell transplant recipients

YILMAZ E., Erdogmus A., Ucan G., Atalay A., ÖZCAN A., PATIROĞLU T., et al.
44th Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation (EBMT), Lisbon, Portekiz, 18 - 21 Mart 2018, cilt.53, ss.557-558, (Özet Bildiri) identifier

25. Engraftment Follow Up with New CBC Parameters of The Children in Hematopoietic Stem Cell Transplantation

KARAKÜKCÜ M., ÜNAL E., Ucan G., ÖZCAN A., PATIROĞLU T.
44th Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation (EBMT), Lisbon, Portekiz, 18 - 21 Mart 2018, cilt.53, ss.628-629, (Özet Bildiri) identifier

26. ALLOGENEIC BONE MARROW TRANSPLANTATION IN THREE CASES WITH DOCK 8 DEFICIENCY

PATIROĞLU T., CANSEVER M., ÖZCAN A., UÇAN G., KELEŞ S., ÜNAL E., et al.
32nd European Immunogenetics and Histocompatibility Conference, Venice, İtalya, 9 - 12 Mayıs 2018, ss.38-388, (Özet Bildiri)

27. TPOG-NÖROBLASTOM 2009 PROTOKOLU: YÜKSEK RISK GRUBU- OTOLOG KÖK HÜCRE TRANSPLANTASYONU TEDAVI KOLU GÜNCEL ÖN SONUÇLARI

AKSOYLAR S., ÇEÇEN R. E., EMİR S., GÜLER E., ÜNAL E., DEMİRAĞ B., et al.
XX. Ulusal Pediatrik Kanser Kongresi, BELEK-ANTALYA, Türkiye, 2 - 06 Mayıs 2018, (Özet Bildiri)

28. Çocukluk Çağı Malign Over Tümörleri: Çok Merkezi 60 Olgunun Değerlendirilmesi

AKYOL Ş., ÇAKMAKÇI S., KARA B., ACIPAYAM C., TUNCEL D. A., DURMUŞ H. S., et al.
XX. Ulusal Pediatrik Kanser Kongresi, Antalya, Türkiye, 2 - 06 Mayıs 2018, (Tam Metin Bildiri)

29. TPOG-Nöroblastom 2009 Protokolü: Yüksek Risk Grubu-Otolog Kök Hücre Transplantasyonu Tedavi Kolu Güncel ön Sonuçları

AKSOYLAR S., ÇEÇEN R. E., emir s., GÜLER E., ÜNAL E., DEMİRAĞ B., et al.
XX. ULUSAL PEDİATRİK KANSER KONGRESİ, Türkiye, 2 - 06 Mayıs 2018, (Tam Metin Bildiri)

30. TPOG NÖROBLASTOMA 2009 PROTOKOL YÜKSEK RİSK GRUBU OYOLOG KÖK HÜCRE TEDAVİ KOLU GÜNCEL SONUÇLAR

AKSOYLAR S., ÇEÇEN R. E., GÜLER E., ÜNAL E., ÜNAL E., DEMİRAĞ B., et al.
UKK 2018, Türkiye, 2 - 05 Mayıs 2018, (Tam Metin Bildiri)

31. Group 3 Innate Lymphoid Cells in DOCK8 Deficiency: From Mice to Human

EKEN A., Okuş F., PATIROĞLU T., Erdem Ş., KARAKÜKCÜ M., CANSEVER M., et al.
Işıl Barlan İmmün Yetmezlikler Sempozyumu, İstanbul, Türkiye, 19 - 20 Nisan 2018, (Tam Metin Bildiri)

32. HEMOPHILIA A HASTALARINDA F8 GEN MUTASYON SPEKTRUMU: 21 YENİ MUTASYON TANIMLAMASI

ATİK T., IŞIK E., AKGÜN B., ONAY H., KAVAKLI R. K., ÖZBEK N. Y., et al.
15. International Hemophilia Congress of Turkey, Istanbul, Türkiye, 14 - 17 Nisan 2018, ss.94-95, (Tam Metin Bildiri)

33. Dedicator of cytokinesis 8 defektif hastalarda grup 3 innate lenfoid hücreleri eksikliği mevcuttur

EKEN A., Okuş F., PATIROĞLU T., Erdem Ş., KARAKÜKCÜ M., CANSEVER M., et al.
4. Klinik İmmunoloji Kongresi, Antalya, Türkiye, 11 - 14 Nisan 2018, (Özet Bildiri)

34. Absence of group 3 innate Iymphoid cells in DOCK8- defective HIES patients

EKEN A., PATIROĞLU T., Okuş F. Z., Erdem Ş., KARAKÜKCÜ M., Cansever M., et al.
The World Immune Regulation Meeting XII (WIRM XII) kongresi, Davos, İsviçre, 14 - 17 Mart 2018, ss.66, (Tam Metin Bildiri)

35. THREE CASES WITH HYPERIMMUNLOBULIN E SYNDROMEDIAGNOSIS DEPENDENT ON DOCK 8 MUTATION THAT AREMADE ALLOGENIC BONE MARROW TRANSPLANTATION

CANSEVER M., ÖZCAN A., Uçan G., VURAL A., KELEŞ S., ÜNAL E., et al.
4. Erciyes Pediatri Akademisi Kış Kongresi, Türkiye, 22 - 24 Şubat 2018, (Özet Bildiri)

36. NON-TRAUMATIC INTRACRANIAL HEMORRHAGES; CASE PRESENTATIONS

ACER H., ÖZCAN A., Saracoglu S., DÖNMEZ H., ÜNAL E., GÜMÜŞ H., et al.
4. Erciyes Pediatri Akademisi Kış Kongresi, Kayseri, Türkiye, 22 - 24 Şubat 2018, ss.16, (Özet Bildiri)

37. CHILDHOOD THROID CANCERS: RESULTS IN A SINGLE CENTER STUDY

KART K. K., KARA B., GÜNDÜZ M., KARA GEDİK G., BUĞRUL F., ÜNAL E., et al.
4. ERCİYES PEDİATRİ AKADEMİSİ KIŞ KONGRESİ, Türkiye, 22 - 24 Şubat 2018, (Özet Bildiri) Sürdürülebilir Kalkınma

38. HEMOFİLİ A HASTALARINDA F8 GEN MUTASYON SPEKTURUMU: 18 YENİ MUTASYON TANIMLANMASI

ATİK T., IŞIK E., AKGÜN B., ONAY H., ÇULHA V., SEZGİN EVİM M., et al.
3. Hematolojik Genetik Sempozyumu, Türkiye, 14 - 16 Şubat 2018

39. Mutation spectrum of F8 gene in Turkish hemophilia A patients: identification of 14 novel mutations

ATİK T., IŞIK E., ÖZBEK N. Y., AKGÜN B., KAVAKLI R. K., ONAY H., et al.
EAHAD 2018 Congress, Madrid, Spain, Madrid, İspanya, 01 Şubat 2018, cilt.24, ss.124, (Tam Metin Bildiri)

40. Novel Mutations in RASGRP1 Are Associated with Immune Dysregulation and Predispose to EBV-Induced Lymphoma

SOMEKH I., MARQUARDT B., LIU Y., ROHLFS M., FRIZINSKY S., ÜNAL E., et al.
American Society of Hematology, SAN DIAGO, Amerika Birleşik Devletleri, 1 - 04 Aralık 2017, cilt.130, ss.2287, (Tam Metin Bildiri)

41. Hastane Kaynaklı Amfoterisin B Dirençli Aspergillus flavus’xxa Bağlı Osteomyelit Olgusu

Erdoğmuş N. A., ATALAY M. A., KOÇ A. N., ÖZCAN A., SARAÇOĞLU S., PATIROĞLU T., et al.
10. Uluslararası Sterilizasyon Dezenfeksiyon Kongresi, 29 Kasım - 03 Aralık 2017, (Tam Metin Bildiri)

42. Hastane kaynaklı amfoterisin B dirençli Aspergillus flavus'a bağlı osteomyelit olgusu

ERDOĞMUŞ N. A., ATALAY M. A., KOÇ A. N., ÖZCAN A., SARAÇOĞLU S., PATIROĞLU T., et al.
10. Uluslararası Sterilzasyon Dezenfeksiyon Kongresi, Antalya, Türkiye, 29 Kasım - 03 Aralık 2017, ss.251-252, (Tam Metin Bildiri)

43. DOCK 8 MUTASYONUNA BAĞLI HİPERİMMUNGLOBULİN E SENDROMU TANISI İLE ALLOJENİK KEMİK İLİĞİ NAKLİ YAPILAN ÜÇ OLGU

CANSEVER M., ÖZCAN A., UÇAN G., VURAL A., KELEŞ S., ÜNAL E., et al.
24.ULUSAL ALLERJİ İMMUNOLOJİ KONGRESİ, Türkiye, 18 - 22 Kasım 2017, (Özet Bildiri)

44. Hepatosplenic Fungal Infections in Children with Leukemia, Risk Factors and Outcome: A Multicentric Study

PATIROĞLU T., ÜNAL E.
Society of pediatric Oncology congress, Türkiye, 17 - 19 Kasım 2017, (Özet Bildiri)

45. Bilateral Auriküler Kitle-Hiperimmünglobülin E Sendromu

VURAL A., NURSAÇAN C. O., KARA I., KETENCİ I., KARAKÜKCÜ M., PATIROĞLU T., et al.
39.Türk ulusal Kulak Burun Boğaz ve Baş Boyun Cerrahisi Kongresi, Antalya, Türkiye, 8 - 12 Kasım 2017, ss.25, (Tam Metin Bildiri)

46. Her tekrarlayan hışıltı astım mıdır?

HANGÜL M., ÖNAL Ö., ÖZCAN A., ÜNAL E., KÖSE M.
Çocuk Göğüs Hastalıkları 2. Kongresi, İstanbul, Türkiye, 27 - 29 Eylül 2017, (Özet Bildiri)

47. Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of 65 Patient

TÜFEKÇİ Ö., KOÇAK Ü., KAYA Z., YENİCESU İ., ALBAYRAK C., ALBAYRAK D., et al.
EHA, 22 - 27 Haziran 2017, (Özet Bildiri)

48. JUVENILE MYELOMONOCYTIC LEUKEMIA IN TURKEY: A RETROSPECTIVE ANALYSIS OF 65 PATIENTS

TÜFEKÇİ Ö., KOÇAK Ü., KAYA Z., Yenicesu I., Albayrak C., Albayrak D., et al.
22nd Congress of the European-Hematology-Association, Madrid, İspanya, 22 - 25 Haziran 2017, cilt.102, ss.769, (Özet Bildiri) identifier

49. THE PROGNOSTIC EFFECT OF CDKN2B-AS, HDAC9, NINJ2, NAA25 POLYMORPHISMS IN CHILDREN WITH ACUTE ARTERIAL ISCHEMIC STROKE: RESULTS IN A REFERENCE CENTER AT MIDDLE ANATOLIA, TURKEY

bozbolat a., ÜNAL E., topaloğlu t., TAHERİ S., bayram kaçar a., ÖZCAN A.
erciyes medical journal, 16 - 19 Mayıs 2017, (Tam Metin Bildiri)

50. HAPLOIDENTICAL HEMATOPOIETIC STEM CELL TRANSPLANTATION WITH DEPLETION OF TCR AB() IN CHILDREN:ERCIYES PEDIATRIC BMT CENTER

KARAKÜKCÜ M., ÜNAL E., YILMAZ E., ÖZCAN A., KÖSE S., UÇAN G., et al.
EHA, 18 Mayıs 2017, (Özet Bildiri)

51. PNÖMEKTOMİ VE LOBEKTOMİ SONRASI KEMİK İLİĞİ NAKLİ YAPILAN ÇOCUK OLGU

KÖSE M., ÖZCAN A., YILMAZ E., SARAÇOĞLU S., ÜNAL E., PATIROĞLU T., et al.
11.ULUSAL PEDİATRİK HEMATOLOJİ KONGRESİ, Türkiye, 4 - 07 Mayıs 2017, (Özet Bildiri)

52. ALFA/BETA HÜCRE AZALTILMIŞ, GAMA/DELTA T HÜCRE VE NK HÜCRE ZENGİNLEŞTİRİLMİŞ DONÖR LENFOSİT İNFÜZYONU

KARAKÜKCÜ M., ÜNAL E., KAYNAR L., ÖZCAN S., KARASU G., ÖZDEMİR M. A., et al.
11.ULUSAL PEDİATRİK HEMATOLOJİ KONGRESİ, Türkiye, 4 - 07 Mayıs 2017, (Özet Bildiri)

53. ÇOCUKLARDA TCR AB() AZALTILMIŞ HAPLOİDENTİK KEMİK İLİĞİ NAKLİ:ERCİYES PEDİATRİK KİT DENEYİMİ

KARAKÜKCÜ M., ÜNAL E., YILMAZ E., ÖZCAN A., UÇAN G., PATIROĞLU T.
11.ULUSAL PEDİATRİK HEMATOLOJİ KONGRESİ, Türkiye, 4 - 07 Mayıs 2017, (Özet Bildiri)

54. XLF EKSİKLİĞİ BULUNAN BİR ÇOCUK HASTADA TCR AB() AZALTILMIŞ HAPLOİDENTİK KEMİK İLİĞİ NAKLİ

ÖZCAN A., YILMAZ E., UÇAN G., PATIROĞLU T., ÜNAL E., KARAKÜKCÜ M.
11.ULUSAL PEDİATRİK HEMATOLOJİ ONGRESİ, Türkiye, 4 - 07 Mayıs 2017, (Özet Bildiri)

55. KANAMADAN HEMORAJİK ŞOKAHEMOFİLİ A

ÜNAL E., ÖZDEMİR M. M., ÖZCAN A., ELİF ÜNVER K., KARAKÜKCÜ M., PATIROĞLU T.
14.TÜRKİYE HEMOFİLİ KONGRESİ, Türkiye, 12 - 15 Nisan 2017, (Özet Bildiri)

56. ÇOCUKLARDA KEMOTERAPİNİN NADİR BİR KOMPLİKASYONU:PULMONER EMBOLİ

PATIROĞLU T., KÖSE S., ÖZCAN A., ÜNAL E., KARAKÜKCÜ M., KÖSE M., et al.
14.TÜRKİYE HEMOFİLİ KONGRESİ, Türkiye, 12 - 15 Nisan 2017, (Özet Bildiri)

57. YENİDOĞAN DÖNEMİNDE KASABACH-MERRİTT SENDROMUNA YOL AÇANKONJENİTAL DEV HEMANJİOMOLGUSU

CEYLAN M., ÖZSOY N. S., ÖZDEMİR A., ÖZCAN A., DÖNMEZ H., ÜNAL E., et al.
25. ULUSAL NEONATOLOJİ KONGRESİ, Türkiye, 12 - 16 Nisan 2017, (Özet Bildiri)

58. Alpha/Beta T cell depleted Donor Lymphocyte Infusion

KAYNAR L., KARAKÜKCÜ M., ÜNAL E., ÖZCAN S., TEZCAN KARASU G., ACAR M. B.
43rd Annual Meeting of the European Society for Blood and Marrow Transplantation, 26 - 29 Mart 2017, ss.86, (Özet Bildiri) identifier

59. Discovery of the First Pathogenic Human EPO Mutation Provides Mechanistic Insight into Cytokine Signaling

Kim A. R., Ulirsch J. C., Wilmes S., ÜNAL E., Moraga I., KARAKÜKCÜ M., et al.
58th Annual Meeting and Exposition of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 3 - 06 Aralık 2016, cilt.128, (Özet Bildiri) identifier

60. Constitutive mismatch repair defect syndrome: New insights from whole exome sequencing data and functional studies

Caglayan A. O., Omay Z. E. E., Koksal Y., Coskun S., ÜNAL E., PER H., et al.
European Biotechnology Conference, Letonya, 5 - 07 Mayıs 2016, cilt.231, (Özet Bildiri) identifier

61. Immüne reconsruction TCR Alfa Beta epleted Haploidentical Hematopoetic Cell Cell Transplantation in Children Preliminary Result of Reference Centre of Middle Antolia TURKEY

KARAKÜKCÜ M., ÜNAL E., yılmaz e., ÖZCAN A., Uçan G., PATIROĞLU T., et al.
EHA, Kayseri, Türkiye, 09 Temmuz 1900 - 12 Temmuz 2016, (Özet Bildiri)

62. INVASIVE FUNGAL INFECTIONS IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMİA SINGLE CENTRE EXPRIENCE OF IN TURKEY

PATIROĞLU T., YILMAZ E., ÖZCAN A., ÜNAL E., KARAKÜKCÜ M., ÖZDEMİR M. A.
EHA, Kayseri, Türkiye, 9 - 12 Temmuz 2016, (Özet Bildiri)

63. CERECRAL STROKE IN A CHİLD WITH CONGENİTAL DYSERYTROPOETİC ANEMİA TYPE II

ÖZCAN A., PATIROĞLU T., ACER H., GÜMÜŞ H., ŞENOL S., KARAKÜKCÜ M., et al.
EHA, Kayseri, Türkiye, 9 - 12 Temmuz 2016, (Özet Bildiri)

64. Chronic mucocutaneous candidiasis with mutation of CARD9 gene mimicking hyperimmunoglobulin E syndrome

PATIROĞLU T., GÜNGOR EKE H., GRIMBACHER B., ÜNAL E.
Meeting of the European-Academy-of-Allergy-and-Clinical-Immunology Location: Vienna, AUSTRIA Date: JUN 11-15, 2016, 11 - 15 Haziran 2016, (Özet Bildiri)

65. CEREBRAL STROKE IN A CHILD WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE II

ÖZCAN A., PATIROĞLU T., ACER H., GÜMÜŞ H., ŞENOL S., KARAKÜKCÜ M., et al.
21st Congress ofthe European Hematology Association Copenhagen, Denmark, June 9 - 12, 2016, 9 - 12 Haziran 2016, (Tam Metin Bildiri)

66. INHIBITOR TO FIBRINOGEN WITHOUT PROPHYLACTIC THERAPY IN A PATIENT WITH CONGENITAL AFIBRINOGENEMIA A CASE REPORT

PATIROĞLU T., YILMAZ E., ÜNAL E., KARAKÜKCÜ M., ÖZDEMİR M. A.
21st Congress of the European-Hematology-Association Location: Copenhagen, DENMARK Date: JUN 09-12, 2016, 9 - 12 Haziran 2016, (Tam Metin Bildiri)

67. Invasive Fungal Infections in Children with Acute Lymphoblastic Leukemia Single Center Experience in Turkey

PATIROĞLU T., YILMAZ E., ÖZCAN A., ÜNAL E., KARAKÜKCÜ M., ÖZDEMİR M. A.
21st Congress of the European-Hematology-Association Location: Copenhagen, DENMARK Date: JUN 09-12, 2016 , 9 - 12 Haziran 2016, (Tam Metin Bildiri)

68. WISCOTT ALDRICH SYNDROME IN A GIRL WHAT IS THE MYSTERY

AKDEMİR A., WİTZEL M., PATIROĞLU T., ÖZDEMİR M. A., KARAKÜKCÜ M., KLEIN C., et al.
21st Congress of the European-Hematology-Association Location: Copenhagen, DENMARK Date: JUN 09-12, 2016 , 9 - 12 Haziran 2016, (Tam Metin Bildiri)

69. Fibromuscular Dysplasia Complicated With Cerebral Stroke in a Child With Congenital Dyserythropoietic Anemia Type II

ÖZCAN A., PATIROĞLU T., ACER H., GÜMÜŞ H., ŞENOL S., KARAKÜKCÜ M., et al.
21st Congress of the European-Hematology-Association Location: Copenhagen, DENMARK Date: JUN 09-12, 2016, 9 - 12 Haziran 2016, (Tam Metin Bildiri)

70. Constitutional Mismatch Repair Defect Syndrome New Insights from Whole Exome Sequencing Data and Functional Studies

Çağlayan A. O., Omay Z. E., Çoskun S., Ünal E., Köksal Y., Per H., et al.
European Biotechnology Congress 2016, Vilniaus, Litvanya, 5 - 07 Mayıs 2016, (Tam Metin Bildiri)

71. Çocukluk çağı nörofibromatozis tip 1 olgularına eşlik eden tümörler Erciyes Üniversitesi deneyimi

PER H., KAÇAR BAYRAM A., GÖRKEM S. B., GÜMÜŞ H., CANPOLAT M., ÜNAL E., et al.
18.Ulusal çocuk nöroloji kongresi, Türkiye, 20 - 24 Nisan 2016, (Özet Bildiri)

72. THE ROLE OF HLA TYPING TO DIAGNOSE MATERNAL ENGRAFTMENT SYNDROME IN PATIENTS WITH SEVERE COMBINED IMMUNE DEFICIENCY

PATIROĞLU T., BEKTAŞ F., ÖZCAN A., ÜNAL E.
30th European Immunogenetics and Histocompatibility Conference, Kos Island, Greece, May 11–14, 2016, 11 - 14 Nisan 2016, (Tam Metin Bildiri)

73. TcR Depleted Haploidentical Hematopoietic StemCell Transplantation in Children The Single CenterExperiences

KARAKÜKCÜ M., ÜNAL E., YILMAZ E., ÖZCAN A., UÇAN G., PATIROĞLU T., et al.
42nd Annual Meeting of the European Societyfor Blood and Marrow TransplantationValencia, Spain3–6 April 2016, 3 - 06 Nisan 2016, (Tam Metin Bildiri)

74. Immune Reconstitution of TCR Depleted Haploidentical Hematopoietic Stem Cell Transplantation in Children Preliminary Results of a Reference Center in Middle Anatolia Turkey

KARAKÜKCÜ M., ÜNAL E., YILMAZ E., ÖZCAN A., UÇAN G., PATIROĞLU T., et al.
42nd Annual Meetingof the European Society forBlood and Marrow Transplantation 3–6 April 2016 Valencia, Spain, 3 - 06 Nisan 2016, (Tam Metin Bildiri)

75. TcR alpha beta Depleted Haploidentical Hematopoietic Stem Cell Transplantation in Children The Single Center Experiences

KARAKÜKCÜ M., ÜNAL E., YILMAZ E., ÖZCAN A., UÇAN G., PATIROĞLU T., et al.
42nd Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation Location: Valencia, SPAIN Date: APR 03-06, 2016 , 3 - 06 Nisan 2016, (Tam Metin Bildiri)

76. Immune Reconstitution of TCR alpha beta Depleted Haploidentical Hematopoietic Stem Cell Transplantation in Children Preliminary Results of a Reference Center in Middle Anatolia Turkey

KARAKÜKCÜ M., ÜNAL E., YILMAZ E., ÖZCAN A., UÇAN G., PATIROĞLU T., et al.
42nd Annual Meeting of the European Societyfor Blood and Marrow Transplantation Valencia, Spain 3–6 April 2016, 3 - 06 Nisan 2016, (Tam Metin Bildiri)

77. Oxidative stress and anti oxidant capacity in hematopoietic stem cell transplantation performed children

KARAKÜKCÜ M., KARAKÜKÇÜ Ç., ÜNAL E., ÖZCAN A., UÇAN G., PATIROĞLU T., et al.
42nd Annual Meetingof the European Society for Blood and Marrow Transplantation 3–6 April 2016 Valencia, Spain, 3 - 06 Nisan 2016, (Özet Bildiri)

78. The mesenchymal stem cell therapy for steroid refractory acute graft versus host disease in Children a Multicenter Survey by the Turkish Pediatric Bone Marrow Transplantation Study Group TPBMT SG

KARAKÜKCÜ M., ÖZTÜRK G., ERBEY M. F., UYGUN V., KARASU G., ATAY D., et al.
42nd Annual Meetingof the European Society for Blood and Marrow Transplantation 3–6 April 2016 Valencia, Spain, 3 - 06 Nisan 2016, (Tam Metin Bildiri)

79. ÇOCUKLARDA TCR AB AZALTILMIŞ HAPLOİDENTİK KÖK HÜCRE TARNSPLANTASYONU

KARAKÜKCÜ M., ÜNAL E., PATIROĞLU T., ÖZDEMİR M. A.
9.ULUSAL KEMİK İLİĞİ TRANSPLANTASYONU VE KÖK HÜCRE TEDAVİLERİ KONGRESİ, Kayseri, Türkiye, 3 - 05 Mart 2016, ss.139, (Özet Bildiri)

80. ÇOK YÜKSEK RİSKLİ NÖROBLASTOM HASTALARINDA TANDEM YÜKSEK DOZ MIBG VE OTOLOG HEMATOPOETİK KÖK HÜCRE NAKLİ

ÜNAL E., KARAKÜKCÜ M., YILMAZ E., UÇAN G., ÖZCAN A., PATIROĞLU T., et al.
9.ULUSAL KEMİK İLİĞİ TRANSPLANTASYONU VE KÖK HÜCRE TEDAVİLERİ KONGRESİ, Türkiye, 3 - 05 Mart 2016, (Özet Bildiri)

81. B ALL HÜCRE DİZİSİNDE TCR AB DEPLESE DLI TCR AB TCR IDELTA VE NK HÜCRELERİNİN BLASTLAR ÜZERİNE ETKİLERİ

KARAKÜKCÜ M., ÜNAL E.
9.ULUSAL KEMİK İLİĞİ TRANSPLANTASYONU VE KÖK HÜCRE TEDAVİLERİ KONGRESİ, Kayseri, Türkiye, 3 - 05 Mart 2016, (Özet Bildiri)

82. DİSTROFİK EPİDERMOLİZİS BÜLLOSADA ALLOJENİK VE MEZENKİMAL KÖK HÜCRE TEDAVİSİ

KARAKÜKCÜ M., YILMAZ E., UÇAN G., ÖZDEMİR M. A., PATIROĞLU T., ÜNAL E.
9.ULUSAL KEMİK İLİĞİ TRANSPLANTASYONU VE KÖK HÜCRE TEDAVİLERİ KONGRESİ, Türkiye, 3 - 05 Mart 2016, (Özet Bildiri)

83. ÇOCUKLARDA HEMATOPOETİK KÖK HÜCRE NAKLİNDE OKSİDATİF HASAR VE ANTİOKSİDAN KAPASİTE

KARAKÜKCÜ M., KARAKÜKCÜ Ç., ÜNAL E., ÖZCAN A., UÇAN G., PATIROĞLU T., et al.
9.ULUSAL KEMİK İLİĞİ TRANSPLANTASYONU VE KÖK HÜCRE TEDAVİLERİ KONGRESİ, 3 - 05 Mart 2016, (Özet Bildiri)

84. ÇOCUKLUK ÇAĞI REFRAKTER AKUT GVHH TEDAVİSİNDE MEZENKİMAL KÖK HÜCRE KULLANIMI

KARAKÜKCÜ M., ÖZTÜRK G., KARASU G., UYGUN V., ERBEY M. F., ÇAKI KILIÇ S., et al.
9.ULUSAL KEMİK İLİĞİ TRANSPLANTASYONU VE KÖK HÜCRE TEDAVİLERİ KONGRESİ, Kayseri, Türkiye, 3 - 05 Mart 2016, (Özet Bildiri)

85. Hurler sendromu tanılı iki hastada hematopoetik kök hücre nakli

YILMAZ E., KARAKÜKCÜ M., KARDAŞ F., ÜNAL E., UÇAN G., PATIROĞLU T., et al.
9.ULUSAL KEMİK İLİĞİ TRANSPLANTASYONU VE KÖK HÜCRE TEDAVİLERİ KONGRESİ, Türkiye, 3 - 05 Mart 2016, (Tam Metin Bildiri)

86. LUPUS ANTICOAGULANT-HYPOPROTHROMBINEMIA SYNDROME IN A 7-YEAR OLD GIRL: A CASE REPORT

PATIROĞLU T., YILMAZ E., ÜNAL E., KARAKÜKCÜ M., ÖZDEMİR M. A.
20th Congress of European-Hematology-Association, Viyana, Avusturya, 11 Haziran 2015 - 14 Ocak 2016, ss.1700, (Tam Metin Bildiri)

87. Pediatric CNS Tumors: Result of a reference center in middle Anatolia

TÜMTÜRK A., ÜNAL E., PER H., DOĞANAY S., YILDIZ O. G., ULUTABANCA H., et al.
43rd Annual Meeting of İnternational Society for Pediatric Neurosurgery, İzmir, Türkiye, 4 - 08 Ekim 2015, cilt.31, sa.10, ss.1959, (Tam Metin Bildiri)

88. Pediatric CNC tumors result of areference center in middle Anatolia

abdulfettah t., ÜNAL E., PER H., DOĞANAY S., YILDIZ O. G., ÖZDEMİR M. A., et al.
43. Annual meeting of international society for pediatric Neurosurgery Izmir, Oct 4-8, 2015, 4 - 08 Ekim 2015, cilt.31, ss.1891-1993

89. Acquired Torticollis related to nervous system pathologies in childhood

TÜMTÜRK A., ÜNAL E., KÜÇÜK A., DOĞANAY S., PER H., KUMANDAŞ S., et al.
43rd Annual Meeting of International Society for Pediatric Neurosurgery, 4 - 08 Ekim 2015, sa.10, (Özet Bildiri)

90. HEMATOPOIETIC STEM CELL TRANSPLANTATION IN RELAPSED OR REFRACTORY EXTRACRANIAL PRIMITIVE NEUROECTODERMAL TUMOR OF CHILDREN AND ADOLESCENTS A MULTICENTER SURVEY STUDY

HAZAR V., KARAKÜKCÜ M., KÜPESİZ O. A., KESİK V., ÜNAL E., KOÇAK Ü., et al.
47th CONGRESS OF THEINTERNATIONAL SOCIETY OFPAEDIATRIC ONCOLOGY (SIOP)CAPE TOWN, SOUTH AFRICAOCTOBER 8–11, 2015, 8 - 11 Ekim 2015, (Tam Metin Bildiri)

91. Leukemia cutis mimicking kerion celci a challenging diagnosis for clinicians

KARTAL D., ÇİNAR S. L., kırkaş ö. g., ÜNAL E., BORLU M.
ESPD 2015 summer school, 25 - 27 Temmuz 2015

92. Leukemia cutis mimicking kerion celsi a challenging diagnosis for clinicians

KARTAL D., ÇİNAR S. L., Kırkaş Ö. G., ÜNAL E., BORLU M.
ESPD 2015 Summerschool, 25 - 27 Haziran 2015, (Özet Bildiri)

93. Inherited prothrombotic risk factors in children with intracranial venous thrombosis single center experience in Turkey

PATIROĞLU T., Gonca K., CANPOLAT M., ÜNAL E., DOĞANAY S., KARAKÜKCÜ M., et al.
XXV Congress of the International Society on Thrombosis and Haemostasis, 20 - 25 Haziran 2015, cilt.13, ss.1-997 identifier identifier

94. HEMATOPOIETIC STEM CELL TRANSPLANTATION FOR PRIMARY IMMUNE DEFICIENY DISEASES: A SINGLE CENTER EXPERIENCE

PATIROĞLU T., KARAKÜKCÜ M., ÜNAL E., AKAR H. H., ÖZDEMİR M. A.
20th Congress of European-Hematology-Association, Viyana, Avusturya, 11 - 14 Haziran 2015, (Tam Metin Bildiri)

95. ANALYSIS OF THERAPY RESULTS IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKAEMIA. A SINGLE CENTER EXPERIENCE IN TURKEY

PATIROĞLU T., ÖZDEMİR M. A., ÜNAL E., DEĞİRMENCİ K., KARAKÜKCÜ M.
20th Congress of European-Hematology-Association, Viyana, Avusturya, 11 - 14 Haziran 2015, ss.1618, (Tam Metin Bildiri)

96. EFFECTIVENESS OF ANKAFERD BLOOD STOPPER IN PROPHYLAXIS AND TREATMENT OF ORAL MUCOSITIS SEEN IN CHILDHOOD CANCERS AND CORRELATION WITH PLASMA CITRULLINE LEVELS

PATIROĞLU T., ŞAHİN N., ÜNAL E., KENDİRCİ M., ÖZDEMİR M. A., KARAKÜKCÜ M.
20th Congress of European-Hematology-AssociationLocation: Vienna, AUSTRIADate: JUN 11-14, 2015, 11 - 14 Haziran 2015, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

97. A rare cause of ptosis in four years old girl Superior mediastinal malignant peripheral nevre sheath tumor

CANPOLAT M., KONTAŞ O., KAYA ÖZÇORA G. D., ÜNAL E., KAÇAR BAYRAM A., KÜÇÜKAYDIN M., et al.
11th European Paediatric Neurology Society (EPNS) Congress, 27 - 30 Mayıs 2015, cilt.19, ss.91-92

98. THE INFLUENCE OF METHYLENETETRAHYDROFOLATEREDUCTASE MTHFR POLYMORPHISMS ON THESIDE EFFECTS OF MEDIUM DOSE METHOTREXATEINFUSION IN CHILDREN WITH ACUTE LYMPHOBLASTICLEUKEMIA

KARAKÜKCÜ M., ÜNAL E., FT M., ÖZDEMİR M. A., PATIROĞLU T., ÖZKUL Y.
XXVIIIth International Symposium on Technological Innovations in Laboratory Hematology., 19 - 21 Mayıs 2015, (Özet Bildiri)

99. THE IMPORTANCE OF NUCLEATED RED BLOOD CELLSIN PATIENTS WITH BETA THALASSEMIA MAJORAND COMPARISON OF TWO AUTOMATED SYSTEMSWITH MANUAL MICROSCOPY AND FLOW CYTOMETRY

KARAKÜKCÜ M., CİĞDEM K., ÜNAL E., ÖZTÜRK A., PATIROĞLU T., ÖZDEMİR M. A.
XXVIIIth International Symposium on Technological Innovations in Laboratory Hematology., 19 - 21 Mayıs 2015, (Özet Bildiri)

100. Prognostic factors and long term outcome after autologous hematopoietic stem cell transplantation in refractory or recurrent Hodgkin s lymphoma of children and adolescents a multicenter survey of Turkish Pediatric BMT Study Group

KESİK V., ATAŞ E., KARAKÜKCÜ M., AKSOYLAR S., ERBEY M. F., TAÇYILDIZ N., et al.
41st Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation, 22 - 25 Mart 2015, (Tam Metin Bildiri)

101. Hematopoietic Stem Cell Transplantation in Relapsed or Refractory Extracranial Primitive Neuro-Ectodermal Tumor of Children and Adolescents: a Multicenter Survey by the Turkish Pediatric Bone Marrow Transplantation Study Group (TPBMT-SG)

HAZAR V., KARAKÜKCÜ M., KÜPESİZ A., KESIK V., ÜNAL E., KOÇAK Ü., et al.
41st Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation,, İstanbul, Türkiye, 22 - 25 Mart 2015, ss.380, (Tam Metin Bildiri)

102. Allogeneic stem cell transplantation in children with relapsed and refractory leukemia

KAYA Z., KARAKÜKCÜ M., ÜNAL E., KOÇAK Ü., YENİCESU İ., GURSEL T.
41st Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation,, İstanbul, Türkiye, 22 - 25 Mart 2015, (Tam Metin Bildiri)

103. Anti-cancer and anti-viral effect of TcR alpha beta(+) depleted DLI: Lessons learned from three children and utility for further indications

KARAKÜKCÜ M., ÜNAL E., MUTLU F. T., YILMAZ E., IŞIK B., GÜL KIRKAŞ Ö., et al.
41st Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation,, İstanbul, Türkiye, 22 - 25 Mart 2015, ss.526, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

104. The mesenchymal stem cells as salvage treatment for refractory acute graft versus host disease in pediatric patients: a Multicenter Survey by the Turkish Pediatric Bone Marrow Transplantation Study Group (TPBMT-SG)

KARAKÜKCÜ M., ÖZTÜRK G., UYGUN V., ERBEY F., KARASU G., DALOĞLU H., et al.
41st Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation,, İstanbul, Türkiye, 22 - 25 Mart 2015, ss.525, (Tam Metin Bildiri)

105. Evaluation of risk factors and outcomes of invasive fungal infections in the first six months after allogeneic hematopoietic stem cell transplantation in pediatric acute leukemia: A Turkish multicenter study

HAZAR V., KARASU G., ÖZTÜRK G., KILIÇ S., UYGUN V., KARAKÜKCÜ M., et al.
41st Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation, İstanbul, Türkiye, 22 - 25 Mart 2015, (Tam Metin Bildiri)

106. Haploidentical Hematopoietic Stem Cell Transplantation with Depletion of TcR alpha beta (+) in Children: Erciyes Pediatric BMT Center

ÜNAL E., KARAKÜKCÜ M., MUTLU F. T., YILMAZ E., IŞIK B., GÜL KIRKAŞ Ö., et al.
41st Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation,, İstanbul, Türkiye, 22 - 25 Mart 2015, ss.704, (Tam Metin Bildiri)

107. Allogeneic bone marrow and mesenchymal stem cells therapy for dystrophic epidermolysis bullosa

KARAKÜKCÜ M., YILMAZ E., KURTOĞLU S., ÖZDEMİR M. A., PATIROĞLU T., ÜNAL E.
41st Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation, İstanbul, Türkiye, 22 - 25 Mart 2015, (Tam Metin Bildiri)

108. Comparison of Cellular Immune Reconstitution for two different method of Haploidentical Hematopoietic Stem Cell Transplantation in children (Post Transplantation Cyclophosphamide versus Negative Depletion of TcR alpha beta(+)); Preliminary results

KARAKÜKCÜ M., UYGUN V., ÜNAL E., KARASU G. T., PATIROĞLU T., ÖZDEMİR M. A., et al.
41st Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation,, İstanbul, Türkiye, 22 - 25 Mart 2015, ss.710, (Tam Metin Bildiri)

109. Sıngle center registry of rare bleedıng dısorders from Turkey

PATIROĞLU T., ÖZDEMİR M. A., KARAKÜKCÜ M., ÜNAL E.
19th Congress of the European Hematology Association, Milan, İtalya, 12 - 15 Haziran 2014, ss.52-54, (Tam Metin Bildiri)

110. Concomitant therapy of a hemophilia-a patient with inhibitor by using low dose by-pass agents

PATIROĞLU T., ÖZDEMİR M. A., IŞIK B., ÜNAL E., KARAKÜKCÜ M.
19th Congress of the European Hematology Association, Milan, İtalya, 12 - 15 Haziran 2014, ss.96-98, (Tam Metin Bildiri)

111. Kemoterapiye sekonder mukozal hasarda sitrülin düzeyleri ve ankaferd kullanımının oral mükozit ve sitrülin düzeyleri üzerine oloan etkisi

PATIROĞLU T., ERDOĞ ŞAHİN N., ÜNAL E., KENDİRCİ M., ÖZDEMİR M. A., KARAKÜKCÜ M.
4. Pediatrik Hematoloji sempozyumu, Eskişehir, Türkiye, 30 Mayıs - 01 Haziran 2014, ss.83, (Tam Metin Bildiri)

112. TWO CASES OF GUILLAIN BARRE SYNDROME DEVELOPED AFTER HEMATOPOIETIC STEM CELL TRANSPLANTATION

KARAKÜKCÜ M., KAYNAR L., ÜNAL E., ESER B., ÖZDEMİR M. M., Cetin M., et al.
40th Annual Meeting of the European-Group-for-Blood-and-Marrow-Transplantation, Milan, İtalya, 30 Mart - 02 Nisan 2014, cilt.49, (Özet Bildiri) identifier

113. IDIOPATHIC PNEUMONIA SYNDROME COMPLICATED WITH PULMONARY HYPERTENSION IN A CHILD AFTER HEMATOPOIETIC STEM CELL TRANSPLANTATION TREATED WITH BOSENTAN AND STEROID

Gul-Kirkas O., Koser N., ÜNAL E., KÖSE M., BAYKAN A., DOĞANAY S., et al.
40th Annual Meeting of the European-Group-for-Blood-and-Marrow-Transplantation, Milan, İtalya, 30 Mart - 02 Nisan 2014, cilt.49, (Özet Bildiri) identifier

114. Inherited Biallelic Loss-Of-Function Mutations In CSF3R Define a Novel Type Of Severe Congenital Neutropenia With Full Myeloid Cell Maturation and Refractoriness To RhG-CSF

Triot A., Jaervinen P. M., Arostegui J. I., Racek T., Puchalka J., Diaz J. L. D., et al.
55th Annual Meeting of the American-Society-of-Hematology, Louisiana, Amerika Birleşik Devletleri, 7 - 10 Aralık 2013, cilt.122, (Özet Bildiri) identifier

115. Wiskott Aldrich Syndrome A Case Report

AYDINBELGE M., DOĞAN S., GÜNDÜZ G., ÜNAL E., PATIROĞLU T.
FDI Annual World Dental Congress, 28 - 30 Ağustos 2013

116. Idiopathic CD4+ lymphocytopenia complicated with diffuse large B-cell lymphoma in two Turkish pediatric patients

PATIROĞLU T., KARAKÜKCÜ M., ÜNAL E., MUTLU F. T.
EFI meeting, Maastricht, Hollanda, 11 - 14 Nisan 2013, ss.44-45, (Tam Metin Bildiri)

117. The experience of pediatric allogeneic hematopoietic stem cell transplantation: Results from a single center at middle Anatolia, Turkey

PATIROĞLU T., KARAKÜKCÜ M., ÜNAL E., MUTLU F. T.
EFI meeting, Maastricht, Hollanda, 11 - 14 Nisan 2013, ss.32-35, (Tam Metin Bildiri)

118. Clinical experience of granulocyte transfusion in the management of pediatric patients with febrile neutopenia: retrospective study from a reference center in Turkey

PATIROĞLU T., KARAKÜKCÜ M., ÜNAL E., MUTLU F. T.
EFI meeting, Maastricht, Hollanda, 11 - 14 Nisan 2013, ss.2-4, (Tam Metin Bildiri)

119. Pansitopeni ile başvuran metilmalonik asidemi : vaka sunumu

Baştuğ O., Ozturk M. A., Korkmaz L., Memur Ş., Halis H., Kardaş F., et al.
21. Ulusal Neonatoloji Kongresi ( UNEKO-21), Antalya, Türkiye, 1 - 04 Nisan 2013, ss.260, (Tam Metin Bildiri)

120. Non-Wılms Renal Tumors In Chıldren Are Stıll A Challenge

PATIROĞLU T., ÖZDEMİR M. A., MUTLU F. T., ÜNAL E., KARAKÜKCÜ M.
Ped Blood and Cancer, Hong-Kong, Çin, 01 Ocak 2013, ss.242, (Tam Metin Bildiri)

121. AML Hastalarında MDM2 SNP309 Polimorfizminin Değerlendirilmesi

AKALIN H., ÖNAL M. G., AKBAROVA Y., SAR Ş., ÜNAL E., KAYNAR L., et al.
10. ULUSAL TIBBİ GENETİK KONGRESİ, Bursa, Türkiye, 13 Ekim - 23 Aralık 2012, (Özet Bildiri)

122. Pediatrik Hastalarda Galaktomannan Antijenemi Testinin Değerlendirilmesi

SAV H., ATALAY M. A., KOÇ A. N., ÜNAL E., DEMİR G., ZARARSIZ G.
XXXV. Türk Mikrobiyoloji Kongresi, Aydın, Türkiye, 1 - 04 Kasım 2012, ss.327, (Tam Metin Bildiri)

123. Serabral aspergillozun çeşitli yöntemlerle erken tanısı: olgu sunumu

SAV H., ATALAY M. A., ÜNAL E., Demir G., ÖZDEMİR M. A., KOÇ A. N.
27. ANKEM Antibiyotik ve Kemoterapi Kongresi, Muğla, Türkiye, 25 - 29 Nisan 2012, ss.3, (Tam Metin Bildiri)

124. Galaktomannan, 1,3- Beta–D-glukan ve PCR testlerinde bronkoalveolar lavaj örneğinin önemi: Olgu sunumu

SAV H., ATALAY M. A., ÜNAL E., KOÇ A. N.
1. Klinik Mikrobiyoloji Kongresi, Antalya, Türkiye, 12 - 16 Kasım 2011, (Tam Metin Bildiri)

125. Neonatal hemofagositik lenfohistiositoz olgusu

Sarıcı D., KURTOĞLU S., Akın M. A., Karakukcu M., Ünal E., Sayılmaz Ö.
19. Ulusal Neonatoloji Kongresi ( UNEKO -19), Muğla, Türkiye, 1 - 04 Nisan 2011, ss.372-373, (Tam Metin Bildiri)

126. Beş Yaşındaki Kız Hastada Williams Beuren Sendromu ve Akut Lenfoblastik Lösemi Birlikteliği

PATIROĞLU T., ÖZCAN A., KARAKÜKCÜ M., ÖZDEMİR M. A., ÜNAL E.
XVI. TPOG Ulusl Pediatrik Kanser Kongresi, Samsun, Türkiye, 18 - 22 Mayıs 2010, ss.161, (Özet Bildiri)

127. Otoimmün Lenfoproliferatif Sendromlu Çocuk Hastada Mikofenolat Mofetil Kullanımına Bağlı Gelişen Pseudotümör Serebri

PATIROĞLU T., ÖZCAN A., KARAKÜKCÜ M., ÖZDEMİR M. A., POYRAZOĞLU H. G., CANPOLAT M., et al.
XVI. TPOG Ulusl Pediatrik Kanser Kongresi, Samsun, Türkiye, 18 - 22 Mayıs 2010, ss.204, (Özet Bildiri)
Kitaplar 13

1. Hematolog-Hemofili

Kardaş N., TUNCEL D. A., KARAKURT N., DEMİR A. M., ATİK T., Avcı Durmuşoğlu E., et al.
Galenos Yayınevi Tic. Ltd. Şti., İstanbul, 2022

2. Çocuklarda boyun kanserlerinde kemoterapi ve radyoterapi.

GÖK V., ÜNAL E.
Çocuklarda Boyun Kitleleri, KETENCİ İBRAHİM, Editör, Türkiye Klinikleri, Ankara, ss.79-86, 2022

3. Nörokutan Hastalıkların Hematolojik-Onkolojik Bulguları ve Yönetimi

GÖK V., ÜNAL E.
Temel Pediatrik Nöroloji Tanı ve Tedavi, KUMANDAŞ SEFER, CANPOLAT MEHMET, Editör, Akademisyen Yayın evi, Ankara, ss.945-954, 2022

4. HEMOFİLİDE İZLEM VE DEĞERLENDİRME

GÖK V., ÜNAL E.
HematoLog Hemofili, MUHLİS CEM AR, Editör, GALENOS, İstanbul, ss.180-188, 2022

5. NÜTRİSYONEL ANEMİ ve BESLENME YÖNETİMİ

GÖK V., AYDIN F., ÜNAL E.
ÇOCUK KRONİK HASTALIKLARINDA BESLENME -1- Çocuk Gastroenteroloji ve Beslenme Çocuk Nefroloji ve Beslenme Çocuk Hematoloji ve Onkolojide Beslenme Cilt Hastalıkları ve Beslenme, Prof. Dr. Yusuf Kenan Haspolat, Prof. Dr. Coşkun Çeltik, Prof. Dr. Kürşat Bora Çarman, Doç. Dr. Ulaş Emre Akbulut, Uzm. Dr. Taşkın Taş, Editör, Orient, Ankara, ss.439-450, 2021

6. Rare Diseases in Children: Focusing on Rare Diseases Pediatric Immunolgy, Neurology

Per H. (Editör), Ünal E. (Editör), Paç Kısaarslan A. (Editör), Karakükçü M. (Editör)
Nobel Yayınevi, Ankara, 2020

7. Dock8 Mutasyonuna Bağlı Hiprimmünglobulin E Sendromu Tanısı ile Allojenik Kemik İliği Nakli Yapılan Üç Olg

PATIROĞLU T., CANSEVER M., ÖZCAN A., UÇAN G., VURAL A., KELEŞ S., et al.
ÇOCUK HEMATOLOJİ-ONKOLOJİİDE OLGULAR, Prof.Dr. Tülin Tiraje Celkan, Editör, Galenos Yayınevi, ss.467-470, 2020

8. T lymphocyte-specific protein tyrosine kinasedeficiency

erdem s., ÜNAL E., EKEN A.
Rare Diseases in Children Focusing on Pediatric Immunology Neurology, Musa Karakükçü, Hüseyin Per, Ekrem Ünal, Ayşenur Paç Kısaarslan, Editör, Nobel Tıp Kitabevi, Ankara, ss.9-16, 2020

9. Bölüm 15 Adelösan ve Genç Erişkin Kanserleri

ÜNAL E., KÖKSAL Y.
Principles and Practice of Pediatric Oncology, 7e, Nur Olgun, Tezer KUTLUK, Editör, Otıp, ss.433-453, 2018

10. Sayısal Lökosit Bozukluklarına yaklaşım (Lökositoz-Lökopeni ile Giden Hastalıklarda Algoritma)

KARAKÜKCÜ M., ÜNAL E., ÖZCAN A.
Türk Pediatrik Hematoloji Derneği Eğitim Serisi V Lökosit Hastalıkları, Ören Hale, Karakaş Zeynep, Koç Ahmet, Özbek Namık Kemal, Editör, Galenos, İstanbul, ss.209-220, 2017

11. KONSÜLTASYON HEMATOLOJİSİ

KARAKÜKCÜ M., ÜNAL E.
TPHD EĞİTİM SERİSİ 2, HALE ÖREN,TİRAJE CELKAN,NAMIK ÖZBEK, Editör, TÜRK PEDİATRİK HEMATOLOJİ DERNEĞİ, Ankara, ss.473-482, 2016

12. Hematoloji-Onkoloji Hastalarında Endokrin Aciller

PATIROĞLU T., ÜNAL E., KARAKÜKCÜ M.
Çocuklarda Acil Endokrin Hastalıklar, Kurtoğlu S, Editör, Nobel Tıp Kitabecleri, İstanbul, ss.315-330, 2014

13. Erkek yenidoğanın zor doğumu

ÜNAL E.
Klinik Olgu Çözümleri Hematoloji, McCann S, Foa R, Smith O, Conneally E (Çeviri editörü: Çetin M), Editör, Nobel Kitabevi, Adana, ss.126-132, 2012
Metrikler

Yayın

385

Yayın (WoS)

228

Yayın (Scopus)

207

Atıf (WoS)

2068

H-İndeks (WoS)

23

Atıf (Scopus)

3115

H-İndeks (Scopus)

29

Atıf (Scholar)

4838

H-İndeks (Scholar)

36

Atıf (TrDizin)

3

H-İndeks (TrDizin)

1

Atıf (Diğer Toplam)

3

Proje

20

Açık Erişim

35
BM Sürdürülebilir Kalkınma Amaçları