Endocrinological Evaluations of a Neurofibromatosis Type 1 Cohort: Is it Necessary to Evaluate Autoimmune Thyroiditis in Neurofibromatosis Type 1?

by Serhat Güler, Gözde Yeşil, Hasan Önal
Published 2017-12-01

Pseudohypoparathyroidism Type Ia with Normocalcemia

by Esra KUTLU, İlker Tolga ÖZGEN, Yaşar CESUR, Gözde YEŞİL
Published 2019-04-01

A Case with Laron Syndrome

by İlker Tolga ÖZGEN, Esra KUTLU, Yaşar CESUR, Gözde YEŞİL
Published 2019-07-01

Early Diagnosis of Fanconi-Bickel Syndrome and a Novel Mutation inSLC2A2 Gene

by Ezgi Çelikboya, Mehmet Şerif Cansever, Tanyel Zübarioğlu, Gözde Yeşil, Nurver Akıncı
Published 2019-09-01

Evaluation of the parents’ anxiety levels before and after the diagnosis of their child with a rare genetic disease: the necessity of psychological support

by Ayse B. Kolemen, Enes Akyuz, Ali Toprak, Erdem Deveci, Gozde Yesil
Published 2021-09-01

Expanding the Phenotype of Homozygous KCNMA1 Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy

by Gözde Yeşil, Ayşe Aralaşmak, Enes Akyüz, Dilara İçağasıoğlu, Türkan Uygur Şahin, Yavuz Bayram
Published 2018-08-01

Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

by Burcu Sevinç Rüstemoğlu, Bedia Samanci, Fatih Tepgeç, Murat Kürtüncü, Umut Altunoglu, Tuncay Gündüz, Gözde Yeşil, Şahin Avcı, Hakan Gürvit, Başar Bilgiç, Güven Toksoy, Mefkure Eraksoy, Haşmet Hanağası, Zehra Oya Uyguner
Published 2021-09-01