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The Journal of Clinical Endocrinology and Metabolism|January 1, 1993
Treatment of familial male precocious puberty with spironolactone, testolactone, and deslorelinL Laue, J Jones, K M Barnes, et al.The Journal of Pediatrics|January 1, 1996
Thyroid abnormalities in children infected with human immunodeficiency virusS Hirschfeld, L Laue, G B Cutler, et al.The Journal of Pediatrics|October 1, 1990
Growth and neuroendocrine dysfunction in children with acquired immunodeficiency syndromeL Laue, P A Pizzo, K Butler, et al.Radiology|November 1, 1984
Pituitary and ovarian abnormalities demonstrated by CT and ultrasound in children with features of the McCune-Albright syndromeK G Rieth, F Comite, T H Shawker, et al.The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
A randomized, cross-over trial of once-daily versus twice-daily parathyroid hormone 1-34 in treatment of hypoparathyroidismK K Winer, J A Yanovski, B Sarani, et al.The Journal of Pediatrics|January 1, 1985
Effect of hydrocortisone dose schedule on adrenal steroid secretion in congenital adrenal hyperplasiaJ Winterer, G P Chrousos, D L Loriaux, et al.Hormone Research|July 1, 1982
Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associationsG P Chrousos, D L Loriaux, D Mann, et al.Endocrine Journal|January 9, 1999
Mutations of the CYP21 gene in nonclassical steroid 21-hydroxylase deficiency in JapanT Tajima, K Fujieda, J Nakae, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 18, 2001
Evidence for decreased growth hormone in patients with hypothalamic hamartoma due to Pallister-Hall syndromeP Feuillan, K F Peters, G B Cutler, et al.The Journal of Clinical Endocrinology and Metabolism|March 1, 1996
Overnight growth hormone concentrations are usually normal in pubertal children with idiopathic short stature--a Clinical Research Center studyS R Rose, G Municchi, K M Barnes, et al.Pageof 25