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The Journal of Clinical Endocrinology and Metabolism|December 13, 2003
Is the thyrotropin-releasing hormone test necessary in the diagnosis of central hypothyroidism in childrenAmeeta Mehta, Peter C Hindmarsh, Richard G Stanhope, et al.European Journal of Pediatrics|May 13, 2016
Management of Cushing syndrome in children and adolescents: experience of a single tertiary centreMaria Güemes, Philip G Murray, Caroline E Brain, et al.Best Practice & Research. Clinical Endocrinology & Metabolism|June 15, 2010
Holistic management of DSDCaroline E Brain, Sarah M Creighton, Imran Mushtaq, et al.Clinical Endocrinology|January 17, 2007
Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasiaLin Lin, Peter C Hindmarsh, Louise A Metherell, et al.Nature Genetics|March 8, 2011
Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone lossMichael A Simpson, Melita D Irving, Esra Asilmaz, et al.JCI Insight|February 9, 2022
Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiencySinéad M McGlacken-Byrne, Ignacio Del Valle, Polona Le Quesne Stabej, et al.Journal of the Endocrine Society|November 24, 2022
A Single-Center, Observational Study of 607 Children and Young People Presenting With Differences of Sex Development (DSD)Elim Man, Imran Mushtaq, Angela Barnicoat, et al.Journal of the Endocrine Society|January 9, 2019
Predicted Benign and Synonymous Variants in <i>CYP11A1</i> Cause Primary Adrenal Insufficiency Through MissplicingAvinaash Maharaj, Federica Buonocore, Eirini Meimaridou, et al.Pageof 1