Showing results (61-70 of 231) with videos related to
Sort By:
Pageof 24
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1984
HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylationP C White, M I New, B DupontProceedings of the National Academy of Sciences of the United States of America|July 1, 1986
Structure of human steroid 21-hydroxylase genesP C White, M I New, B DupontTrends in Endocrinology and Metabolism: TEM|April 18, 2001
Apparent mineralocorticoid excessR C Wilson, S Nimkarn, M I NewThe Journal of Pediatrics|April 1, 1981
Familial nephrotic syndrome and focal segmental glomerulosclerosisM Chandra, J Mouradian, J R Hoyer, et al.The Journal of Steroid Biochemistry and Molecular Biology|December 1, 1993
Molecular cloning of multiple cDNAs encoding human enzymes structurally related to 3 alpha-hydroxysteroid dehydrogenaseK N Qin, M I New, K C ChengThe Journal of Clinical Endocrinology and Metabolism|June 1, 1976
Dehydroepiandrosterone sulfate (DS) levels, a rapid test for abnormal adrenal androgen secretionS Korth-Schutz, L S Levine, M I NewActa Endocrinologica|June 1, 1976
Evidence for the adrenal source of androgens in precocious adrenarcheS Korth-Schutz, L S Levine, M I NewThe 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 WhiteEndocrine Research|January 1, 1989
Clinical and genetic characterization of nonclassic 21-hydroxylase deficiencyP W Speiser, M I New, P C WhiteThe American Journal of Cardiology|March 31, 1976
Nomograms relating aldosterone excretion to urinary sodium and potassium in the pediatric population: their application to the study of childhood hypertensionM I New, C J Baum, L S LevinePageof 24