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Clinics in Perinatology|September 1, 1994
Prenatal diagnosis and management of congenital adrenal hyperplasiaP W Speiser, M I NewChest|December 1, 1991
Pulmonary embolism. Efficacy of D-dimer and thrombin-antithrombin III complex determinations as screening tests before lung scanningT Leitha, W Speiser, R DudczakAdvances in Pediatrics|July 14, 2012
Treatment outcomes in congenital adrenal hyperplasiaTina Q Cheng, Phyllis W SpeiserEndocrine Reviews|June 17, 2000
Congenital adrenal hyperplasia due to 21-hydroxylase deficiencyP C White, 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 WhiteThe 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 SpeiserKidney International|May 1, 1994
Functional characterization of cytokine autoantibodies in chronic renal failure patientsG Sunder-Plassmann, S Kapiotis, C Gasche, et al.Pageof 52