Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature von Kaygusuz, Sare Betul, Alavanda, Ceren, Kirkgoz, Tarik, Eltan, Mehmet, Yavas Abali, Zehra, Helvacioglu, Didem, Guran, Tulay, Ata, Pinar, Bereket, Abdullah, Turan, Serap

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Low DHEAS Concentration in a Girl Presenting with Short Stature and Premature Pubarche: A Novel PAPSS2 Gene Mutation von Eltan, Mehmet, Yavas Abali, Zehra, Arslan Ates, Esra, Kirkgoz, Tarik, Kaygusuz, Sare Betul, Türkyılmaz, Ayberk, Bereket, Abdullah, Turan, Serap, Guran, Tulay

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A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age von Eltan, Mehmet, Alavanda, Ceren, Yavas Abali, Zehra, Ergenekon, Pinar, Yalındag Ozturk, Nilufer, Sakar, Mustafa, Dagcinar, Adnan, Kirkgoz, Tarik, Kaygusuz, Sare Betul, Gokdemir, Yasemin, Elcioglu, Huriye Nursel, Guran, Tulay, Bereket, Abdullah, Ata, Pinar, Turan, Serap

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Total oxidant and antioxidant status and paraoxonase 1 levels of children with noncystic fibrosis bronchiectasis von Gedik, Ahmet Hakan, Cakir, Erkan, Vehapoglu Turkmen, Aysel, Ozer, Omer Faruk, Kaygusuz, Sare Betul

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Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity von Turan, Serap, Mumm, Steven, Alavanda, Ceren, Kaygusuz, Betul Sare, Gurpinar Tosun, Busra, Arman, Ahmet, Huskey, Margaret, Guran, Tulay, Duan, Shenghui, Bereket, Abdullah, Whyte, Michael P.

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Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly Con... von Kırkgöz, Tarık, Eltan, Mehmet, Kaygusuz, Sare Betül, Yavaş Abalı, Zehra, Helvacıoğlu, Didem, Seven Menevşe, Tuba, Gürpınar Tosun, Büşra, Güran, Tülay, Bereket, Abdullah, Turan, Serap

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Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects von Kaygusuz, Sare Betul, Ates, Esra Arslan, Vignola, Maria Lillina, Volkan, Burcu, Geckinli, Bilgen Bilge, Turan, Serap, Bereket, Abdullah, Gaston-Massuet, Carles, Guran, Tulay

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Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects von Kaygusuz, Sare Betul, Ates, Esra Arslan, Vignola, Maria Lillina, Volkan, Burcu, Geckinli, Bilgen Bilge, Turan, Serap, Bereket, Abdullah, Gaston-Massuet, Carles, Guran, Tulay

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Catch-up Growth and Discontinuation of Fludrocortisone Treatment in Aldosterone Synthase Deficiency von Gurpinar Tosun, Busra, Kendir Demirkol, Yasemin, Seven Menevse, Tuba, Kaygusuz, Sare Betul, Ozbek, Mehmet Nuri, Altincik, Selda Ayca, Mammadova, Jamala, Cayir, Atilla, Doger, Esra, Bayramoglu, Elvan, Nalbantoglu, Ozlem, Yesiltepe Mutlu, Gul, Aghayev, AghaRza, Turan, Serap, Bereket, Abdullah, Guran, Tulay

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Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature von Abali, Zehra Yavas, Yesil, Gozde, Kirkgoz, Tarik, Kaygusuz, Sare Betul, Eltan, Mehmet, Turan, Serap, Bereket, Abdullah, Guran, Tulay

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FOXA2 as a Candidate Gene Responsible for Congenital Panhypopituitarism: A Review of the Literature von Correia, Jorge César, Corral, Laura Gómez, Kaygusuz, Sare Betül, Gualtieri, Angelica, Gaston-Massuet, Carles

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Supplementary Materials of Clinical and Molecular Genetic Characteristics of the Patients with Hereditary Hypophosphatemia Supplementary Documents von Eltan, Mehmet, Alavanda, Ceren, Abali, Zehra, Gurpinar Tosun, Busra, Kurt, Ilknur, Kirkgoz, Tarik, Guven, Sercin, Kaygusuz, Sare Betul, Abali, Saygin, Helvacioglu, Didem, guran, tulay, Gokce, Ibrahim, Arman, Ahmet, Bereket, Abdullah, Ata, Pinar, Turan, Serap

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Supplementary Figure 1 von Kaygusuz, Sare Betul, Ates, Esra Arslan, Vignola, Maria Lillina, Volkan, Burcu, Geckinli, Bilgen Bilge, Turan, Serap, Bereket, Abdullah, Gaston-Massuet, Carles, Tulay Guran

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Supplementary Figure 2 von Kaygusuz, Sare Betul, Ates, Esra Arslan, Vignola, Maria Lillina, Volkan, Burcu, Geckinli, Bilgen Bilge, Turan, Serap, Bereket, Abdullah, Gaston-Massuet, Carles, Tulay Guran

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Supplemantal Figure 1. LC-MS/MS determination of DOC, corticosterone and aldosterone over time in three ASD patients after discontinuation of fludrocortisone treatment von Gurpinar Tosun, Busra, Kendir Demirkol, Yasemin, Seven Menevse, Tuba, Kaygusuz, Sare Betul, Ozbek, Mehmet Nuri, Altıncık, Selda Ayça, Mamadova, Jamala, Cayir, Atilla, Doger, Esra, Bayramoglu, Elvan, Nalbantoğlu, Özlem, Yesiltepe Mutlu, Gul Yesiltepe, Aghayev, AghaRza, Turan, Serap, Bereket, Abdullah, Guran, Tulay

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Adrenocortical carcinoma in atypical Beckwith-Wiedemann syndrome due to loss of methylation at imprinting control region 2 von Eltan, Mehmet, Arslan Ates, Esra, Cerit, Kivilcim, Menevse, Tuba Seven, Kaygusuz, Sare Betul, Eker, Nursah, Bagci, Pelin, Ergelen, Rabia, Turan, Serap, Bereket, Abdullah, Guran, Tulay

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