Arş. Gör. Seher POLAT

Yayın Ağı

Makaleler 5

1. A Nonvirilized form of Classic 3 beta-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria

ALİKAŞİFOĞLU A., Buyukyilmaz G., GÖNÇ E. N., ÖZÖN Z. A., KANDEMİR N., DÜNDAR M., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.281, 2016 (SCI-Expanded, Scopus)

2. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

MENABO S., Polat S., BALDAZZI L., KULLE A. E., HOLTERHUS P., GROETZINGER J., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.22, sa.5, ss.610-616, 2014 (SCI-Expanded, Scopus)

3. Characterisation of three novel CYP11B1 mutations in classic and non-classic 11 beta-hydroxylase deficiency

Polat S., Kulle A., Karaca Z. C., Akkurt I., Kurtoglu S., KELEŞTİMUR F., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , cilt.170, sa.5, ss.697-706, 2014 (SCI-Expanded, Scopus)

4. 17-Alpha Hydroxylase Deficiency: A Rare Case of Primary Amenorrhea and Hypertension

Şimşek Y., POLAT S., Riepe F. G., Diri H., TANRIVERDİ F., ÖZDAMAR KARACA Z. C., et al.

TURKISH JOURNAL OF ENDOCRINOLOGY AND METABOLISM , cilt.18, ss.137-139, 2014 (Scopus)

5. A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients

DÜNDAR M., Kiraz A., Emirogullari E. F., SAATÇİ Ç., Taheri S., BAŞKOL M., et al.

ANNALS OF SAUDI MEDICINE , cilt.32, sa.4, ss.343-348, 2012 (SCI-Expanded, Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 4

1. 11 beta hydroxylase deficiency : functional characterisation of three novel CYP11B1 mutations.

Polat S., Kullle A., Karaca Z., Akkurt İ., KURTOĞLU S., Keleştemur F., et al.

9th Joint Meeting of Pediatric Endocrinology, İtalya, 1 - 04 Eylül 2013, cilt.80, ss.78, (Tam Metin Bildiri)

2. The increasing importance of Medical Genetics in Turkey

POLAT S., Karabulut S. Y., BAHADIR O., DÜNDAR M.

European Biotechnology Congress 2011, İstanbul, Türkiye, 28 Ekim - 01 Kasım 2011, cilt.22, ss.90, (Özet Bildiri)

3. Investigation of PAI-1 4G/5G Polymorphism In Turkish FMF Patients.

ŞENER E. F., TAHERİ S., POLAT S., ZARARSIZ G., SAATÇİ Ç., ÖZKUL Y., et al.

IX. Ulusal Tıbbi Genetik Kongresi., İstanbul, Türkiye, 1 - 04 Aralık 2010, (Tam Metin Bildiri)

4. MEFV Gene Mutations Screening In Turkish Population.

DÜNDAR M., POLAT S., ŞENER E. F., TAHERİ S., Kiraz A., SAATÇİ Ç., et al.

IX. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 1 - 04 Aralık 2010, (Tam Metin Bildiri)

Metrikler

Arş. Gör. Seher POLAT

Yayınlar & Eserler

1. A Nonvirilized form of Classic 3 beta-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria

2. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

3. Characterisation of three novel CYP11B1 mutations in classic and non-classic 11 beta-hydroxylase deficiency

4. 17-Alpha Hydroxylase Deficiency: A Rare Case of Primary Amenorrhea and Hypertension

5. A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients

1. 11 beta hydroxylase deficiency : functional characterisation of three novel CYP11B1 mutations.

2. The increasing importance of Medical Genetics in Turkey

3. Investigation of PAI-1 4G/5G Polymorphism In Turkish FMF Patients.

4. MEFV Gene Mutations Screening In Turkish Population.

Yayın

Yayın (WoS)

Yayın (Scopus)

Atıf (WoS)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Proje

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