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Showing results (151-160 of 292) with videos related to

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Clinical Pharmacology and Therapeutics|July 1, 1981
Effects of growth hormone on antipyrine kinetics in childrenA B Rifkind, P Saenger, L S Levine, et al.
Clinical Endocrinology|December 1, 1979
Serum androgen concentrations in neonates and young infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyS Pang, L S Levine, D M Chow, et al.
Human Mutation|January 1, 1994
Mutations in steroid 21-hydroxylase (CYP21)P C White, M T Tusie-Luna, M I New, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1977
Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasiaS Pang, J Hotchkiss, A L Drash, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1977
Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertensionM I New, L S Levine, E G Biglieri, et al.
Clinical Endocrinology|September 1, 1986
Antipyrine clearance in congenital adrenal hyperplasiaS Loche, A B Rifkind, E Stoner, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1971
Congenital adrenal hyperplasia due to deficiency of 11 -hydroxylation of 17 -hydroxylated steroidsM Zachmann, J A Völlmin, M I New, et al.
The Journal of Clinical Investigation|July 1, 1988
Nonsense mutation causing steroid 21-hydroxylase deficiencyH Globerman, M Amor, K L Parker, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1988
Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiencyM Amor, K L Parker, H Globerman, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1979
"Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasiaM I New, F Lorenzen, S Pang, et al.
Pageof 30

Showing results (151-160 of 292) with videos related to

Sort By:
Pageof 30
Clinical Pharmacology and Therapeutics|July 1, 1981
Effects of growth hormone on antipyrine kinetics in childrenA B Rifkind, P Saenger, L S Levine, et al.
Clinical Endocrinology|December 1, 1979
Serum androgen concentrations in neonates and young infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyS Pang, L S Levine, D M Chow, et al.
Human Mutation|January 1, 1994
Mutations in steroid 21-hydroxylase (CYP21)P C White, M T Tusie-Luna, M I New, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1977
Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasiaS Pang, J Hotchkiss, A L Drash, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1977
Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertensionM I New, L S Levine, E G Biglieri, et al.
Clinical Endocrinology|September 1, 1986
Antipyrine clearance in congenital adrenal hyperplasiaS Loche, A B Rifkind, E Stoner, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1971
Congenital adrenal hyperplasia due to deficiency of 11 -hydroxylation of 17 -hydroxylated steroidsM Zachmann, J A Völlmin, M I New, et al.
The Journal of Clinical Investigation|July 1, 1988
Nonsense mutation causing steroid 21-hydroxylase deficiencyH Globerman, M Amor, K L Parker, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1988
Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiencyM Amor, K L Parker, H Globerman, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1979
"Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasiaM I New, F Lorenzen, S Pang, et al.
Pageof 30