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Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 22, 2020
Recombinant GH treatment in a case of Costello syndrome with a 5-year follow-upSirmen Kizilcan Cetin, Zeynep Siklar, Elif Ozsu, 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.Therapeutic Advances in Endocrinology and Metabolism|July 15, 2026
Two threats in early life: congenital hyperinsulinemic hypoglycemia and thrombosisIlkyaz Turktan, Sirmen Kızılcan Çetin, Gizem Senyazar, et al.Clinical Endocrinology|November 6, 2007
The effect of growth hormone treatment on bone mineral density in prepubertal girls with Turner syndrome: a multicentre prospective clinical trialZehra Aycan, Ergun Cetinkaya, Feyza Darendeliler, et al.Hormone Research|January 6, 2007
Effects of growth hormone on growth, insulin resistance and related hormones (ghrelin, leptin and adiponectin) in Turner syndromeFeyza Darendeliler, Zehra Aycan, Ergun Cetinkaya, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|March 21, 2008
Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndromeAyça T Ergür, Gönül Ocal, Merih Berberoglu, 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.Diabetes|May 6, 2017
Recessively Inherited <i>LRBA</i> Mutations Cause Autoimmunity Presenting as Neonatal DiabetesMatthew B Johnson, Elisa De Franco, Hana Lango Allen, et al.Genes & Development|March 26, 2003
Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiencyAnne-Marie Pulichino, Sophie Vallette-Kasic, Catherine Couture, et al.Pageof 5