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	41.	CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism. [electronic resource] by Turan, Ihsan Hutchins, B Ian Hacihamdioglu, Bulent Kotan, L Damla Gurbuz, Fatih Ulubay, Ayca Mengen, Eda Yuksel, Bilgin Wray, Susan Topaloglu, A Kemal Producer: 20170911 In: The Journal of clinical endocrinology and metabolism vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant. [electronic resource] by Siklar, Zeynep Ellard, Sian Okulu, Emel Berberoğlu, Merih Young, Elizabeth Savaş Erdeve, Senay Mungan, Ilke Akin Hacihamdioğlu, Bülent Erdeve, Omer Arsan, Saadet Oçal, Gönül Producer: 20120223 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Clinical review of 95 patients with 46,XX disorders of sex development based on the new Chicago classification. [electronic resource] by Öcal, Gönül Berberoğlu, Merih Sıklar, Zeynep Aycan, Zehra Hacıhamdioglu, Bülent Savas Erdeve, Şenay Çamtosun, Emine Kocaay, Pınar Ruhi, Hatice I Kılıç, Birim G Tukun, Ajlan Producer: 20160425 In: Journal of pediatric and adolescent gynecology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders. [electronic resource] by Hacıhamdioğlu, Bülent Oçal, Gönül Berberoğlu, Merih Savaş Erdeve, Senay Camtosun, Emine Kocaay, Pınar Fitoz, Suat Ceyhan, Koray Dindar, Hüseyin Yağmurlu, Aydın Kır, Metin Unal, Emel Sıklar, Zeynep Producer: 20150525 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell. [electronic resource] by Oçal, Gönül Flanagan, Sarah E Hacihamdioğlu, Bülent Berberoğlu, Merih Siklar, Zeynep Ellard, Sian Savas Erdeve, Senay Okulu, Emel Akin, Ilke Mungan Atasay, Begum Arsan, Saadet Yağmurlu, Aydin Producer: 20120223 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development. [electronic resource] by Topcu, Vehap Ilgin-Ruhi, Hatice Siklar, Zeynep Karabulut, Halil Gurhan Berberoglu, Merih Hacihamdioglu, Bulent Savas-Erdeve, Senay Aycan, Zehra Peltek-Kendirci, Havva Nur Ocal, Gonul Tukun, Fatma Ajlan Producer: 20160909 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Worldwide view of nephropathic cystinosis: results from a survey from 30 countries. [electronic resource] by Bertholet-Thomas, Aurélia Berthiller, Julien Tasic, Velibor Kassai, Behrouz Otukesh, Hasan Greco, Marcella Ehrich, Jochen de Paula Bernardes, Rejane Deschênes, Georges Hulton, Sally-Ann Fischbach, Michel Soulami, Kenza Saeed, Bassam Valavi, Ehsan Cobenas, Carlos Jose Hacihamdioglu, Bülent Weiler, Gabrielle Cochat, Pierre Bacchetta, Justine Producer: 20180403 In: BMC nephrology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome. [electronic resource] by Prasad, Rathi Hadjidemetriou, Irene Maharaj, Avinaash Meimaridou, Eirini Buonocore, Federica Saleem, Moin Hurcombe, Jenny Bierzynska, Agnieszka Barbagelata, Eliana Bergadá, Ignacio Cassinelli, Hamilton Das, Urmi Krone, Ruth Hacihamdioglu, Bulent Sari, Erkan Yesilkaya, Ediz Storr, Helen L Clemente, Maria Fernandez-Cancio, Monica Camats, Nuria Ram, Nanik Achermann, John C Van Veldhoven, Paul P Guasti, Leonardo Braslavsky, Debora Guran, Tulay Metherell, Louise A Producer: 20170908 In: The Journal of clinical investigation vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease. [electronic resource] by Jolly, Angad Bayram, Yavuz Turan, Serap Aycan, Zehra Tos, Tulay Abali, Zehra Yavas Hacihamdioglu, Bulent Coban Akdemir, Zeynep Hande Hijazi, Hadia Bas, Serpil Atay, Zeynep Guran, Tulay Abali, Saygin Bas, Firdevs Darendeliler, Feyza Colombo, Roberto Barakat, Tahsin Stefan Rinne, Tuula White, Janson J Yesil, Gozde Gezdirici, Alper Gulec, Elif Yilmaz Karaca, Ender Pehlivan, Davut Jhangiani, Shalini N Muzny, Donna M Poyrazoglu, Sukran Bereket, Abdullah Gibbs, Richard A Posey, Jennifer E Lupski, James R Producer: 20200520 In: The Journal of clinical endocrinology and metabolism vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)