Showing 1 - 19 results of 19 for search 'Huseyin Demirbilek', query time: 0.06s
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The ımportance of art therapy ın the qualıty of lıfe ın hemodıalysıs patıents by Ergün Parmaksız, Hüseyin Demirbilek
Published 2020-10-01
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Cystoscopy-Guided Laparoscopic Excision of Prostatic Utricle: Report of a Case by Ozlem Boybeyi-Turer, Huseyin Demirbilek, Tutku Soyer
Published 2020-01-01
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The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism by Sonya Galcheva, Hüseyin Demirbilek, Sara Al-Khawaga, Khalid Hussain
Published 2019-02-01
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Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the <italic... by Meliha Demiral, Hüseyin Demirbilek, Edip Unal, Ceren Damla Durmaz, Serdar Ceylaner, Mehmet Nuri Özbek
Published 2020-09-01
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Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-Eastern Region of Turkey by Meliha Demiral, Edip Unal, Birsen Baysal, Rıza Taner Baran, Hüseyin Demirbilek, Mehmet Nuri Özbek
Published 2020-09-01
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Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes by Edip Unal, Meliha Demiral, Birsen Baysal, Mehmet Ağın, Elif Gökçe Devecioğlu, Hüseyin Demirbilek, Mehmet Nuri Özbek
Published 2021-03-01
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Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year by Şervan Özalkak, Meliha Demiral, Edip Ünal, Funda Feryal Taş, Hüseyin Onay, Hüseyin Demirbilek, Mehmet Nuri Ozbek
Published 2023-09-01
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The effects of the covid-19 pandemic on puberty: a cross-sectional, multicenter study from Turkey by Gul Yesiltepe Mutlu, Elif Eviz, Belma Haliloglu, Heves Kirmizibekmez, Fatma Dursun, Servan Ozalkak, Atilla Cayir, Beste Yuksel Sacli, Mehmet Nuri Ozbek, Huseyin Demirbilek, Sukru Hatun
Published 2022-08-01
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Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis by Maha Sherif, Hüseyin Demirbilek, Atilla Çayır, Sophia Tahir, Büşra Çavdarlı, Meliha Demiral, Ayşe Nurcan Cebeci, Doğuş Vurallı, Sofia Asim Rahman, Edip Unal, Gönül Büyükyılmaz, Riza Taner Baran, Mehmet Nuri Özbek, Khalid Hussain
Published 2021-03-01
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