Vici syndrome in siblings born to consanguineous parents von Tasdemir, Sener, Sahin, Ibrahim, Cayır, Atilla, Yuce, Ihsan, Ceylaner, Serdar, Tatar, Abdulgani

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Assessment of Executive Function Skills in Children with Isolated Growth Hormone Deficiency: A Cross-sectional Study von Yitik Tonkaz, Gülsüm, Çayır, Atilla

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The clinical and laboratory features of patients with triple A syndrome: a single-center experience in Turkey von Yıldırım, Ruken, Unal, Edip, Tekmenuray-Unal, Aysel, Taş, Funda Feryal, Özalkak, Şervan, Çayır, Atilla, Özbek, Mehmet Nuri

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Is growth hormone deficiency associated with anxiety disorder and depressive symptoms in children and adolescents?: A case-control study von Akaltun, İsmail, Çayır, Atilla, Kara, Tayfun, Ayaydın, Hamza

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A rare cause of primary amenorrhea: LHCGR gene mutations von Aktar Karakaya, Amine, Çayır, Atilla, Unal, Edip, Beştaş, Aslı, Ece Solmaz, Aslı, Kenan Haspolat, Yusuf

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Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal‐recessive hypophosphataemic rickets type 2 von Dursun, Fatma, Turan, İhsan, Bitkin, Eda Çelebi, Bayramoğlu, Elvan, Çayır, Atilla, Erdeve, Şenay Savaş, Çakır, Esra Deniz Papatya, Çamtosun, Emine, Dilek, Semine Ozdemir, Kırmızıbekmez, Heves, Eser, Metin, Türkyılmaz, Ayberk, Karagüzel, Gülay

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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 von Kurnaz, Erdal, Kartal Baykan, Emine, Türkyılmaz, Ayberk, Yaralı, Oğuzhan, Yavaş Abalı, Zehra, Turan, Serap, Bereket, Abdullah, Çayır, Atilla, Guran, Tulay

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A Genetic Approach in the Evaluation of Short Stature von Turkyilmaz, Ayberk, Donmez, Ayse Sena, Cayir, Atilla

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Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study von Akıncı, Ayşehan, Türkkahraman, Doğa, Tekedereli, İbrahim, Özer, Leyla, Evren, Bahri, Şahin, İbrahim, Kalkan, Tarkan, Çürek, Yusuf, Çamtosun, Emine, Döğer, Esra, Bideci, Aysun, Güven, Ayla, Eren, Erdal, Sangün, Özlem, Çayır, Atilla, Bilir, Pelin, Törel Ergür, Ayça, Ercan, Oya

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The Relationship between Psychopathology, Self-esteem, Body Perception and Serum Sex Steroids in Pubertal Gynecomastia von Arslan, Semiha Comertoglu, Esin, Ibrahim Selcuk, Cayır, Atilla, Orbak, Zerrin, Dursun, Onur Burak

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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 von Sherif, Maha, Demirbilek, Hüseyin, Çayır, Atilla, Tahir, Sophia, Çavdarlı, Büşra, Demiral, Meliha, Cebeci, Ayşe Nurcan, Vurallı, Doğuş, Rahman, Sofia Asim, Unal, Edip, Büyükyılmaz, Gönül, Baran, Rıza Taner, Özbek, Mehmet Nuri, Hussain, Khalid

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Effect of Gluten-Free Diet on Serum Antioxidant Levels in Children with Celiac von Gul, Mehmet Ali, Ozgeris, Fatma Betul, Kurt, Nezahat, Volkan, BurcuIslek, Ali, Cayir, V

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Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship von Özsu, Elif, Çetinkaya, Semra, Bolu, Semih, Hatipoğlu, Nihal, Savaş Erdeve, Şenay, Evliyaoğlu, Olcay, Baş, Firdevs, Çayır, Atilla, Dündar, İsmail, Akbaş, Emine Demet, Uçaktürk, Seyid Ahmet, Berberoğlu, Merih, Şıklar, Zeynep, Özalkak, Şervan, Muratoğlu Şahin, Nursel, Keskin, Melikşah, Şiraz, Ülkü Gül, Turan, Hande, Öztürk, Ayşe Pınar, Mengen, Eda, Sağsak, Elif, Dursun, Fatma, Akyürek, Nesibe, Odabaşı Güneş, Sevinç, Aycan, Zehra

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Genetic Forms of Calciopenic Rickets von Donmez, Ayse Sena, Turkyilmaz, Ayberk, Cayir, Atilla

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Comparison of Treatment Regimens in Management of Severe Hypercalcemia Due to Vitamin D Intoxication in Children von Demir, Korcan, Döneray, Hakan, Kara, Cengiz, Atay, Zeynep, Çetinkaya, Semra, Çayır, Atilla, Anık, Ahmet, Eren, Erdal, Uçaktürk, Ahmet, Can Yılmaz, Gülay, Törel Ergür, Ayça, Kendirci, Mustafa, Aycan, Zehra, Bereket, Abdullah, Aydın, Murat, Orbak, Zerrin, Özkan, Behzat

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The effects of the covid-19 pandemic on puberty: a cross-sectional, multicenter study from Turkey von Yesiltepe Mutlu, Gul, Eviz, Elif, Haliloglu, Belma, Kirmizibekmez, Heves, Dursun, Fatma, Ozalkak, Servan, Cayir, Atilla, Sacli, Beste Yuksel, Ozbek, Mehmet Nuri, Demirbilek, Huseyin, Hatun, Sukru

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Is Serum Progranulin Level a Biomarker in Autism and Cognitive Development Disorders? von Özgeriş, Fatma Betül, Kurt, Nezahat, Ibili Ucuz, Ilknur, Koçak Yilmaz, Kübra, Keleş, Mevlüt Sait, Çayir, Atilla, Dursun, Onur Burak

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Combined occurrence of Alström syndrome and bronchiectasis von Kaya, Avni, Orbak, Zerrin, Cayir, Atilla, Döneray, Hakan, Tasdemir, Sener, Ozantürk, Aysegül, Bingöl, Fatih

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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort von 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

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Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience von Esen, İhsan, Bayramoğlu, Elvan, Yıldız, Melek, Aydın, Murat, Karakılıç Özturhan, Esin, Aycan, Zehra, Bolu, Semih, Önal, Hasan, Kör, Yılmaz, Ökdemir, Deniz, Ünal, Edip, Önder, Aşan, Evliyaoğlu, Olcay, Çayır, Atilla, Taştan, Mehmet, Yüksel, Ayşegül, Kılınç, Aylin, Büyükinan, Muammer, Özcabı, Bahar, Akın, Onur, Binay, Çiğdem, Kılınç, Suna, Yıldırım, Ruken, Aytaç, Emel Hatun, Sağsak, Elif

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