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Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 29, 2012
A case of rapid-onset obesity with hypothalamic dysfunction, hypoventilation, autonomic dysregulation, and neural crest tumor: ROHHADNET syndromeAyhan Abaci, Gonul Catli, Erhan Bayram, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 13, 2025
Concerns for mood disorders in children presenting with early menarche is not an indication for pubertal suppressionKübra Yüksek Acinikli, Ozge Besci, Gözde Akın Kağızmanlı, et al.
Human Genetics|January 23, 2022
Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humansA Kemal Topaloglu, Enver Simsek, Matthew A Kocher, 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.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesisHakan Cangul, Zehra Aycan, Halil Saglam, et al.
Clinical Endocrinology|August 20, 2010
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidismHakan Cangul, Neil V Morgan, Julia R Forman, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2015
Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadismYavuz Bayram, Suleyman Gulsuner, Tulay Guran, et al.
The Journal of Clinical Endocrinology and Metabolism|August 16, 2016
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-SituAdeline K Nicholas, Eva G Serra, Hakan Cangul, et al.
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