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Proceedings of the National Academy of Sciences of the United States of America|October 27, 1999
Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excessM I New, R C WilsonEndocrine Reviews|August 1, 1986
Genetics of adrenal steroid 21-hydroxylase deficiencyM I New, P W SpeiserThe Journal of Pediatrics|August 1, 1975
Nephrosonography in the evaluation of renal failure and masses in infantsF G Boineau, J Rothman, J E LewyPediatric Research|April 1, 1981
Renal function in rats with unilateral proteinuria produced by renal perfusion with aminonucleosideM Chandra, J R Hoyer, J E LewyHormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 1, 1994
Enzyme-linked immunosorbent assay (ELISA) method for screening of non-classical steroid 21-hydroxylase deficiencyH Ueshiba, M Zerah, M I NewKidney International|July 1, 1994
Alterations in glomerular dynamics in congenital, unilateral hydronephrosisB G Hanss, J E Lewy, R C VariPediatric Nephrology (Berlin, Germany)|July 1, 1987
Reversible vasoconstriction in rats with congenital unilateral hydronephrosisF G Boineau, R C Vari, J E LewyJournal of the American Society of Nephrology : JASN|February 1, 1993
Angiotensin or thromboxane receptor antagonism in rats with congenital hydronephrosisR C Vari, F G Boineau, J E LewyThe Journal of Clinical Endocrinology and Metabolism|August 1, 1987
Morning salivary 17-hydroxyprogesterone is a useful screening test for nonclassical 21-hydroxylase deficiencyM Zerah, S Y Pang, M I NewImmunological Reviews|October 1, 1985
Adrenal 21-hydroxylase cytochrome P-450 genes within the MHC class III regionP C White, M I New, B DupontPageof 24