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Fatih Gurbuz
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Journal Articles

DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism

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Subject Area:
Endocrinology , Women's and Children's Health
Ihsan Turan, Korcan Demir, Eda Mengen, Leman Damla Kotan, Fatih Gürbüz, Bilgin Yüksel, Ali Kemal Topaloglu
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2021) 94 (9-10): 364–368.
https://doi.org/10.1159/000520409
Published Online: 25 October 2021
View articletitled, DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism
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Journal Articles

Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide

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Subject Area:
Endocrinology , Women's and Children's Health
Eda Mengen, Selma Tunc, L. Damla Kotan, Ozlem Nalbantoglu, Korcan Demir, Fatih Gurbuz, Ihsan Turan, Gül Seker, Bilgin Yuksel, A. Kemal Topaloglu
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2016) 85 (2): 107–111.
https://doi.org/10.1159/000441977
Published Online: 24 November 2015
View articletitled, Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide
Open the PDF for Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide in another window
Journal Articles

The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development

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Subject Area:
Endocrinology , Women's and Children's Health
Bilgin Yüksel, Alexandra E. Kulle, Fatih Gürbüz, Maik Welzel, Damla Kotan, Eda Mengen, Paul-Martin Holterhus, Ali Kemal Topaloğlu, Joachim Grötzinger, Felix G. Riepe
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2013) 80 (3): 163–169.
https://doi.org/10.1159/000354086
Published Online: 01 August 2013
View articletitled, The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development
Open the PDF for The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development in another window