Showing results (151-160 of 198) with videos related to

Sort By:
Pageof 20
Endocrine|May 18, 2025
Comprehensive clinical and molecular characterization with long-term outcomes in 40 patients with congenital hyperinsulinismZehra Yavas Abali, Firdevs Bas, Jayne A L Houghton, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 30, 2020
Clinical Characteristics of 46,XX Males with Congenital Adrenal HyperplasiaŞenay Savaş-Erdeve, Zehra Aycan, Semra Çetinkaya, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 14, 2023
Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as GirlsGuilherme Guaragna-Filho, Gil Guerra-Junior, Rieko Tadokoro-Cuccaro, et al.
European Journal of Pediatrics|December 2, 2008
The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in childrenTulay Guran, Serap Turan, Abdullah Bereket, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 12, 2020
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 InfantsTülay Güran, Başak Tezel, Meltem Çakır, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 15, 2024
Adherence to Growth Hormone Treatment in Children During the COVID-19 PandemicErdal Eren, Semra Çetinkaya, Yasemin Denkboy Öngen, et al.
Journal of Pediatric and Adolescent Gynecology|February 8, 2017
Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 PatientsBanu Kucukemre Aydin, Nurcin Saka, Firdevs Bas, et al.
Clinical Endocrinology|December 15, 2012
Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous communityHakan Cangul, Zehra Aycan, Alvaro Olivera-Nappa, et al.
The Journal of Clinical Endocrinology and Metabolism|March 31, 2017
Birth Weight in Different Etiologies of Disorders of Sex DevelopmentSukran Poyrazoglu, Feyza Darendeliler, S Faisal Ahmed, 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.
Pageof 20