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The Journal of Clinical Endocrinology and Metabolism|January 1, 1987
Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiencyP W Speiser, M I NewEndocrinology and Metabolism Clinics of North America|June 1, 1994
Steroid 11 beta-hydroxylase deficiency and related disordersP C White, P W SpeiserBest Practice & Research. Clinical Endocrinology & Metabolism|June 18, 2002
Long-term consequences of childhood-onset congenital adrenal hyperplasiaPerrin C White, Phyllis W SpeiserEndocrine Reviews|August 1, 1986
Genetics of adrenal steroid 21-hydroxylase deficiencyM I New, P W SpeiserDNA (Mary Ann Liebert, Inc.)|December 1, 1989
Structure of the human RD gene: a highly conserved gene in the class III region of the major histocompatibility complexP W Speiser, P C WhiteLife Sciences|May 19, 1998
Ibuprofen inhibits leukocyte migration through endothelial cell monolayersR Hofbauer, W Speiser, S KapiotisThe Journal of Pediatric Endocrinology|July 1, 1994
Prenatal diagnosis and treatment of congenital adrenal hyperplasiaP W Speiser, M I NewJournal of Pediatric Endocrinology & Metabolism : JPEM|June 11, 2008
Growth hormone improves growth rate and preserves renal function in Dent diseaseSharone Sheffer-Babila, Manju Chandra, Phyllis W SpeiserThe New England Journal of Medicine|July 7, 1988
Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1P W Speiser, M I New, P C WhiteThrombosis Research|February 15, 1986
Sandwich ELISA for t-PA antigen employing a monoclonal antibodyC Korninger, W Speiser, J Wojta, et al.Pageof 18