Aydilek Dağdeviren Çakır

Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

Leman Damla Kotan, Gaëtan Ternier, Aydilek Dağdeviren Çakır et al. · Genetics in Medicine · 2021 · 54 citations · Full text

Infertility, Andrology, Female Infertility +14

Serum vitamin D levels during activation and remission periods of patients with juvenile idiopathic arthritis and familial Mediterranean fever

Aydilek Dağdeviren Çakır, Ahmet Arvas, Kenan Barut et al. · The Turkish Journal of Pediatrics · 2016 · 38 citations · Full text

Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation

Olcay Evliyaoğlu, Oya Ercan, Emel Ataloğlu et al. · Journal of Clinical Research in Pediatric Endocrinology · 2017 · 22 citations · Full text

Genetics, Genetic Epidemiology, Pathology +22

Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

Aydilek Dağdeviren Çakır, Firdevs Baş, Onur Akın et al. · Journal of Clinical Research in Pediatric Endocrinology · 2021 · 18 citations · Full text

Incidence of Type 1 Diabetes in Children Aged Below 18 Years During 2013-2015 in Northwest Turkey

Şükran Poyrazoğlu, Rüveyde Bundak, Zehra Yavaş Abal et al. · Journal of Clinical Research in Pediatric Endocrinology · 2018 · 16 citations · Full text