17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
Siklar, Zeynep, Camtosun, Emine, Bolu, Semih, Yildiz, Melek, Akinci, Aysehan, Bas, Firdevs, Dündar, İsmail, Bestas, Asli, Ünal, Edip, Kocaay, Pinar, Guran, Tulay, Buyukyilmaz, Gonul, Ugurlu, Aylin Kilinc, Tosun, Buşra Gurpinar, Turan, Ihsan, Kurnaz, Erdal, Yuksel, Bilgin, Turkkahraman, Doga, Cayir, Atilla, Celmeli, Gamze, Gonc, E. Nazli, Eklioğlu, Beray Selver, Cetinkaya, Semra, Yilmaz, Seniha Kiremitci, Atabek, Mehmet Emre, Buyukinan, Muammer, Arslan, Emrullah, Mengen, Eda, Cakir, Esra Deniz Papatya, Karaoglan, Murat, Hatipoglu, Nihal, Orbak, Zerrin, Ucar, Ahmet, Akyurek, Nesibe, Akbas, Emine Demet, Isik, Emregül, Kaygusuz, Sare Betul, Sutcu, Zumrut Kocabey, Seymen, Gulcan, Berberoglu, Merih
Published in Endocrine (2024)
Published in Endocrine (2024)
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Antimüllerian Hormone Levels of Infants with Premature Thelarche
Muratoğlu Şahin, Nursel, Bayramoğlu, Elvan, Nursun Özcan, Hatice, Kurnaz, Erdal, Keskin, Melikşah, Savaş-Erdeve, Şenay, Çetinkaya, Semra, Aycan, Zehra
Published in Journal of clinical research in pediatric endocrinology (01.09.2019)
Published in Journal of clinical research in pediatric endocrinology (01.09.2019)
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Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty
Aycan, Zehra, Savaş-Erdeve, Şenay, Çetinkaya, Semra, Kurnaz, Erdal, Keskin, Melikşah, Muratoğlu Şahin, Nursel, Bayramoğlu, Elvan, Ceylaner, Gülay
Published in Journal of clinical research in pediatric endocrinology (01.09.2018)
Published in Journal of clinical research in pediatric endocrinology (01.09.2018)
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Sever’s Disease in a Patient Receiving Growth Hormone with no Causative Relation
Kurnaz, Erdal, Savas-Erdeve, Senay, Aycan, Zehra, Çetinkaya, Semra
Published in Journal of clinical and diagnostic research (01.03.2018)
Published in Journal of clinical and diagnostic research (01.03.2018)
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A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make
Çetinkaya, Semra, Güran, Tülay, Kurnaz, Erdal, Keskin, Melikşah, Sağsak, Elif, Savaş Erdeve, Senay, Suntharalingham, Jenifer P, Buonocore, Federica, Achermann, John C, Aycan, Zehra
Published in Journal of clinical research in pediatric endocrinology (01.03.2018)
Published in Journal of clinical research in pediatric endocrinology (01.03.2018)
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Is Chromosomal Study Necessary for Girls with Inguinal Hernia?
Kurnaz, Erdal, Savas-Erdeve, Senay, Aycan, Zehra
Published in Journal of clinical and diagnostic research (01.08.2016)
Published in Journal of clinical and diagnostic research (01.08.2016)
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A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene
Keskin, Melikşah, Muratoğlu Şahin, Nursel, Kurnaz, Erdal, Bayramoğlu, Elvan, Savaş Erdeve, Şenay, Aycan, Zehra, Çetinkaya, Semra
Published in Journal of clinical research in pediatric endocrinology (01.03.2017)
Published in Journal of clinical research in pediatric endocrinology (01.03.2017)
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Near final height in patients with idiopathic growth hormone deficiency: A single‐centre experience
Kurnaz, Erdal, Çetinkaya, Semra, Aycan, Zehra
Published in Journal of paediatrics and child health (01.11.2018)
Published in Journal of paediatrics and child health (01.11.2018)
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Quantitative evaluation of early retinal changes in children with type 1 diabetes mellitus without retinopathy
Tekin, Kemal, Inanc, Merve, Kurnaz, Erdal, Bayramoglu, Elvan, Aydemir, Emre, Koc, Mustafa, Kiziltoprak, Hasan, Aycan, Zehra
Published in Clinical and experimental optometry (01.09.2018)
Published in Clinical and experimental optometry (01.09.2018)
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Functional assessment of variants associated with Wolfram syndrome
Riachi, Melissa, Yilmaz, Sebahat, Kurnaz, Erdal, Aycan, Zehra, Çetinkaya, Semra, Tranebjærg, Lisbeth, Rendtorff, Nanna Dahl, Bitner-Glindzicz, Maria, Bockenhauer, Detlef, Hussain, Khalid
Published in Human molecular genetics (15.11.2019)
Published in Human molecular genetics (15.11.2019)
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Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency
Kurnaz, Erdal, Kartal Baykan, Emine, Türkyılmaz, Ayberk, Yaralı, Oğuzhan, Yavaş Abalı, Zehra, Turan, Serap, Bereket, Abdullah, Çayır, Atilla, Guran, Tulay
Published in Hormone research in paediatrics (01.04.2021)
Published in Hormone research in paediatrics (01.04.2021)
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Clinical characteristics and molecular genetic analysis of a cohort with idiopathic congenital hypogonadism
Turkyilmaz, Ayberk, Cayir, Atilla, Yarali, Oguzhan, Kurnaz, Erdal, Kartal Baykan, Emine, Arslan Ates, Esra, Demirbilek, Huseyin
Published in Journal of Pediatric Endocrinology & Metabolism (25.06.2021)
Published in Journal of Pediatric Endocrinology & Metabolism (25.06.2021)
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Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene
Kurnaz, Erdal, Savaş Erdeve, Şenay, Çetinkaya, Semra, Aycan, Zehra
Published in Hormone research in paediatrics (01.01.2019)
Published in Hormone research in paediatrics (01.01.2019)
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Systemic Pseudohypoaldosteronism Type 1 due to 3 Novel Mutations in SCNN1Aand SCNN1BGenes
Cayir, Atilla, Demirelli, Yasar, Yildiz, Duran, Kahveci, Hasan, Yarali, Oguzhan, Kurnaz, Erdal, Vuralli, Doğuş, Demirbilek, Huseyin
Published in Hormone research in paediatrics (2019)
Published in Hormone research in paediatrics (2019)
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The Spectrum of Low-Density Lipoprotein Receptor Mutations in a Large Turkish Cohort of Patients with Familial Hypercholesterolemia
Turkyilmaz, Ayberk, Kurnaz, Erdal, Alavanda, Ceren, Yarali, Oguzhan, Kartal Baykan, Emine, Yavuz, Dilek, Cayir, Atilla, Ata, Pinar
Published in Metabolic syndrome and related disorders (01.08.2021)
Published in Metabolic syndrome and related disorders (01.08.2021)
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