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Showing page 1 of results 1 - 10 of about 64 pages

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Follow-up of Individuals with Gender Identity Disorders: A Long and Challenging Process | ESPE2019
Esin Karakilic Ozturan; Ayse Pinar Ozturk; Al Asli Derya Kardelen; Sukran Poyrazoglu; Firdevs Bas; Ayse Burcu Ayaz; Sahika Yukse
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-270
Published: 2019-08-22

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The Clinical Features and Effect of Growth Hormone Treatment in 3-M Syndrome Cases with Severe Growth Retardation | ESPE2019
Öztürk Ayse Pinar; Umut Altunoglu; Özturan Esin Karakiliç; Güven Toksoy; Sükran Poyrazoglu; Firdevs Bas; Oya Uyguner; Feyz
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-195
Published: 2019-08-22

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Two Siblings with Hypophosphatemic Rickets: SLC34A3 Gene Mutations with Different Clinical Phenotypes | ESPE2019
Esin Karakilic-Ozturan; Ayse Pinar Ozturk; Al Asli Derya Kardelen; Sukran Poyrazoglu; Firdevs Bas; Feyza Darendeliler
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-45
Published: 2019-08-22

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Genetic Evaluation of Idiopathic Short Stature | ESPE2019
Birsen Karaman; Firdevs Bas; Adam Najafli; Sahin Avci; Al Asli Derya Kardelen; Güven Toksoy; Umut Altunoglu; Sükran Poyrazoglu
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-390
Published: 2019-08-22

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Genotype-Phenotype Correlation and Clinical Findings in 145 Patients with Congenital Adrenal Hyperplasia: Single Centre Experience | ESPE2019
Gizem Cilsaat; Guven Toksoy; Firdevs Bas; Birsen Karaman; Sukran Poyrazoglu; Oya Uyguner; Seher Basaran; Umut Altinoglu; Feyza D
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-306
Published: 2019-08-22

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Serum Endocan Levels as a Marker of Endothelial Dysfunction in Turner Syndrome and Correlation with Cardiac Findings | ESPE2019
Ali Genco Gencay; Feyza Darendeliler; Kemal Nisli; Serra Karaca; Asli Derya Kardelen; Sükran Poyrazoglu; Firdevs Bas
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-236
Published: 2019-08-22

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Characteristics of puberty, pubertal height gain and final height in children with classical 21 hydroxylase deficiency | ESPE2019
Zehra Yavas Abali; Melek Yildiz; Firdevs Bas; Hasan Onal; Saygin Abali; Gizem Cilsaat; Zehra Oya Uyguner; Serap Turan; Feyza Dar
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-159
Published: 2019-08-22

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Influence of salt supplementation on drug therapy in children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency aged 0-3 years: Update on a retrospective multicentre analysis using the I-CAH registry | ESPE2019
Uta Neumann; der Linde Annelieke van; Ruth Krone; Ayla Guven; Tülay Güran; Heba Elsedfy; Feyza Darendeliler; Tania Bachega; An
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-157
Published: 2019-08-22

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The Investigation of Genetic Etiology in Familial Cases with Congenital Hypothyroidism | ESPE2019
Al Asli Derya Kardelen; Fatma Büsra Isik; Esin Karakiliç Özturan; Mavi Deniz Sözügüzel; Ayse Pinar Öztürk; Sükran Poyra
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-145
Published: 2019-08-22

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Targeted Panel Gene Sequencing for Identification of Genetic Etiology of 46,XY Disorders of Sex Development | ESPE2019
Sukran Poyrazoglu; Guven Toksoy; Agharza Aghayev; Birsen Karaman; Sahin Avci; Umut Altunoglu; Melek Yildiz; Zehra Yavas Abali; F
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-134
Published: 2019-08-22

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