Dr. Öğr. Üyesi VEYSEL GÖK

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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)

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

ÖZÇELİK F., ASLAN K., Gok V., Ari M. B., ÖZCAN A., EKEN A., et al.

Pediatric Hematology and Oncology , cilt.41, sa.4, ss.301-309, 2024 (SCI-Expanded)

Immunodeficiency associated with a novel functionally defective variant of <i>SLC19A1</i> 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) Sürdürülebilir Kalkınma

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) Sürdürülebilir Kalkınma

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) Sürdürülebilir Kalkınma

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)

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) Sürdürülebilir Kalkınma

NOVEL VARIANTS IN ETV6 AND FYB1 GENES: TWO CHILDREN WITH RARE INHERITED THROMBOCYTOPENIA

Gok V., Karaca M., Ozcan A., Yilmaz E., Bozdogan S. T., Bisgin A., et al.

HAEMOPHILIA , ss.118-119, 2022 (SCI-Expanded)

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) Sürdürülebilir Kalkınma

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) Sürdürülebilir Kalkınma

HEMOPHILIA INTERNATIONAL ACCREDITATION TRAINING PLAN IN ERCIYES UNIVERSITY PEDIATRIC HEMATOLOGY CLINIC

Gok V., Kuzucu E. G., Ataseven L., Cuce I., Dogan M. E., Abdulrezzak U., et al.

HAEMOPHILIA , ss.29-30, 2021 (SCI-Expanded)

A CHILD WHO DEVELOPED LUPUS ANTICOAGULANT HYPOPROTHROMBINEMIA SYNDROME AFTER VIRAL GASTROENTERITIS

Gok V., Simsek N., Aydin F., Ozcan A., Yilmaz E., Unal E., et al.

HAEMOPHILIA , ss.148-149, 2021 (SCI-Expanded)

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) Sürdürülebilir Kalkınma

AFIBRINOGENEMIA EXPERIENCE MULTI CENTER STUDY

Tuncel D. A., Gok V., Pekpak E., Tokgoz H., Acipayam C., Yilmaz E., et al.

HAEMOPHILIA , ss.148-149, 2020 (SCI-Expanded)

VON WILLEBRAND DISEASE TYPE 2B MIMICKING AUTOIMMUNE THROMBOCYTOPENIA IN NEONATAL PERIOD

Gok V., Isik E., Yilmaz E., Aydin F., Ozcan A., Unal E., et al.

HAEMOPHILIA , ss.135, 2020 (SCI-Expanded)

MEFV Mutation Frequency in Pediatric Patients with Familial Mediterranean Fever and its Relationship with Clinical Phenotypes in Marmara Region of Turkey

GÖK V., Yigit O., Gayret O. B., Hamilcikan S.

IRANIAN JOURNAL OF PEDIATRICS , cilt.27, sa.3, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Early Weight Loss in Exclusively Breastfed Term Neonates

Hamilcikan S., GÖK V., Bent S., Can E.

IRANIAN JOURNAL OF PEDIATRICS , cilt.27, sa.2, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Diğer Dergilerde Yayınlanan Makaleler

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)

Changes in Body Mass Index and Height Among Survivors of Childhood Acute Lymphoblastic Leukemia: A Single Institutional Experience

Gök V., Mutlu F. T., Karadoğan M.

Türkiye'de Lösemi Lenfoma Miyelom Araştırmaları , cilt.7, sa.2, ss.57-64, 2023 (Hakemli Dergi)

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 , sa.2, ss.207-210, 2023 (ESCI) Sürdürülebilir Kalkınma

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)

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)

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)

Comprehensive approach to hemophilia

Gök V., Ünal E.

JOURNAL OF HEALTH SCIENCES AND MEDICINE , cilt.5, sa.4, ss.1199-1206, 2022 (Hakemli Dergi)

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)

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)

Two Siblings Followed Up for Hereditary Multiple Exostoses

Erol M., Yigit O., Adanir O., Toksoz M., Narin H., GÖK V., et al.

HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI , cilt.52, sa.2, ss.116-119, 2014 (ESCI)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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

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

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

Metrikler

Yayın

Atıf (WoS)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

Yayınlar & Eserler