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Gonul Ocal

Showing results (11-20 of 18) with videos related to

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European Journal of Pediatrics|February 25, 2010
A novel mutation of 5alpha-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignmentSenay Savas Erdeve, Zehra Aycan, Merih Berberoglu, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|January 2, 2004
Evaluation of nutritional status and factors related to malnutrition in children on CAPDMesiha Ekim, Aydan Ikinciogullari, Betul Ulukol, et al.
The Journal of Clinical Endocrinology and Metabolism|April 14, 2005
Severe growth hormone insensitivity resulting from total absence of signal transducer and activator of transcription 5bVivian Hwa, Brian Little, Pelin Adiyaman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 8, 2011
Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantationSenay Savas-Erdeve, Merih Berberoglu, Zeynep Siklar, et al.
Pediatric Endocrinology Reviews : PER|February 1, 2008
5 alpha steroid reductase deficiency in TurkeyPelin Bilir Adiyaman, Gonul Ocal, Ergun Cetinkaya, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 22, 2015
Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex developmentVehap Topcu, Hatice Ilgin-Ruhi, Zeynep Siklar, et al.
American Journal of Human Genetics|January 1, 2013
Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activationSarah E Flanagan, Weijia Xie, Richard Caswell, et al.
The Journal of Clinical Endocrinology and Metabolism|December 15, 2010
Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patientsLaurent Maimoun, Pascal Philibert, Benoit Cammas, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
European Journal of Pediatrics|February 25, 2010
A novel mutation of 5alpha-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignmentSenay Savas Erdeve, Zehra Aycan, Merih Berberoglu, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|January 2, 2004
Evaluation of nutritional status and factors related to malnutrition in children on CAPDMesiha Ekim, Aydan Ikinciogullari, Betul Ulukol, et al.
The Journal of Clinical Endocrinology and Metabolism|April 14, 2005
Severe growth hormone insensitivity resulting from total absence of signal transducer and activator of transcription 5bVivian Hwa, Brian Little, Pelin Adiyaman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 8, 2011
Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantationSenay Savas-Erdeve, Merih Berberoglu, Zeynep Siklar, et al.
Pediatric Endocrinology Reviews : PER|February 1, 2008
5 alpha steroid reductase deficiency in TurkeyPelin Bilir Adiyaman, Gonul Ocal, Ergun Cetinkaya, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 22, 2015
Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex developmentVehap Topcu, Hatice Ilgin-Ruhi, Zeynep Siklar, et al.
American Journal of Human Genetics|January 1, 2013
Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activationSarah E Flanagan, Weijia Xie, Richard Caswell, et al.
The Journal of Clinical Endocrinology and Metabolism|December 15, 2010
Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patientsLaurent Maimoun, Pascal Philibert, Benoit Cammas, et al.
Pageof 2