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Korcan Demir
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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

Serum Level of Biotin Rather than the Daily Dosage Is the Main Determinant of Interference on Thyroid Function Assays

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Subject Area:
Endocrinology , Women's and Children's Health
Ahu Paketçi, Engin Köse, Özlem Gürsoy Çalan, Sezer Acar, Pelin Teke, Ferhat Demirci, Ayhan Abacı, Korcan Demir, Nur Arslan, Ece Böber
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2020) 92 (2): 92–98.
https://doi.org/10.1159/000502740
Published Online: 25 October 2019
View articletitled, Serum Level of Biotin Rather than the Daily Dosage Is the Main Determinant of Interference on Thyroid Function Assays
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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

GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in Adolescents

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Subject Area:
Endocrinology , Women's and Children's Health
Hüseyin Anıl Korkmaz, Tuba Edgünlü, Erdal Eren, Korcan Demir, Esra Deniz Papatya Çakir, Sevim Karakaș Çelik, Behzat Özkan
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2015) 83 (3): 177–182.
https://doi.org/10.1159/000369013
Published Online: 18 December 2014
View articletitled, GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in Adolescents
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Journal Articles

Psychomotor Retardation Caused by a Defective Thyroid Hormone Transporter: Report of Two Families with Different MCT8 Mutations

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Subject Area:
Endocrinology , Women's and Children's Health
Ahmet Anık, Simone Kersseboom, Korcan Demir, Gönül Çatlı, Uluç Yiş, Ece Böber, Alies van Mullem, Ramona E.A. van Herebeek, Semra Hız, Ayhan Abacı, Theo J. Visser
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2014) 82 (4): 261–271.
https://doi.org/10.1159/000365191
Published Online: 18 September 2014
View articletitled, Psychomotor Retardation Caused by a Defective Thyroid Hormone Transporter: Report of Two Families with Different MCT8 Mutations
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Journal Articles

The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study

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Subject Area:
Endocrinology , Women's and Children's Health
Firdevs Baş, Feyza Darendeliler, Zehra Aycan, Ergun Çetinkaya, Merih Berberoğlu, Zeynep Şıklar, Gönül Öcal, Özlem Timirci, Semra Çetinkaya, Şükran Darcan, Damla Gökşen Şimşek, Aysun Bideci, Peyami Cinaz, Ece Böber, Korcan Demir, Abdullah Bereket, Serap Turan, M. Emre Atabek, Filiz Tütüncüler, Turgay İsbir, Nilüfer Bozkurt, Sema Kabataş Eryılmaz, Ozan Uzunhan, Banu Küçükemre Aydın, Rüveyde Bundak
Journal: Hormone Research in Paediatrics
Horm Res Paediatr (2012) 77 (2): 85–93.
https://doi.org/10.1159/000335172
Published Online: 23 March 2012
View articletitled, The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study
Open the PDF for The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study in another window