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Journal of Endocrinological Investigation|January 1, 1989
Growth and final height in classical and nonclassical 21-hydroxylase deficiencyM I New, J M Gertner, P W Speiser, et al.
Journal of Psychosomatic Obstetrics and Gynaecology|September 1, 1996
Mothers' reactions to prenatal diagnostic procedures and dexamethasone treatment of congenital adrenal hyperplasiaP D Trautman, H F Meyer-Bahlburg, J Postelnek, et al.
American Journal of Diseases of Children (1960)|July 1, 1983
Selective hypoaldosteronism in infancy. Report of a caseJ A Curtis, H P Monaghan, M I New, et al.
The New England Journal of Medicine|November 3, 1988
An inherited defect in aldosterone biosynthesis caused by a mutation in or near the gene for steroid 11-hydroxylaseH Globerman, A Rösler, R Theodor, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1995
Steroid 21-hydroxylase deficiency: genotype may not predict phenotypeR C Wilson, A B Mercado, K C Cheng, et al.
Journal of Chromatography|December 28, 1984
Clinical applications of the rapid high-performance liquid chromatographic determination of serum cortisolS Loche, F Porcelli, M Rosen, et al.
The New England Journal of Medicine|January 17, 1991
Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylaseP W Speiser, L Agdere, H Ueshiba, et al.
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