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Showing results (241-250 of 292) with videos related to

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Hypertension (Dallas, Tex. : 1979)|January 1, 1984
Primary hyperaldosteronism in childhood due to unilateral macronodular hyperplasia. Case reportS E Oberfield, L S Levine, A Firpo, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1980
New studies of the 11 beta-hydroxylase and 18-hydroxylase enzymes in the hypertensive form of congenital adrenal hyperplasiaL S Levine, W Rauh, K Gottesdiener, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1993
Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8K M Curnow, L Slutsker, J Vitek, et al.
Biochemistry|February 8, 1994
Natural mutagenesis study of the human steroid 5 alpha-reductase 2 isozymeW C Wigley, J S Prihoda, I Mowszowicz, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1990
Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample studyM Zerah, H Ueshiba, E Wood, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1982
A pilot newborn screening for congenital adrenal hyperplasia in AlaskaS Pang, W Murphey, L S Levine, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1978
Prepubertal diagnosis of steroid 5 alpha-reductase deficiencyP Saenger, A S Goldman, L S Levine, et al.
The International Journal of Pediatric Nephrology|October 1, 1985
Evaluation of percutaneous transluminal renal angioplasty in childhood hypertensionF Fallo, S E Oberfield, L S Levine, et al.
Clinical and Experimental Hypertension. Part A, Theory and Practice|January 1, 1986
Percutaneous transluminal renal angioplasty in the treatment of renovascular hypertension in childrenF Fallo, S E Oberfield, L S Levine, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 7, 1999
Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature reviewM E Damore, P W Speiser, A E Slonim, et al.
Pageof 30

Showing results (241-250 of 292) with videos related to

Sort By:
Pageof 30
Hypertension (Dallas, Tex. : 1979)|January 1, 1984
Primary hyperaldosteronism in childhood due to unilateral macronodular hyperplasia. Case reportS E Oberfield, L S Levine, A Firpo, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1980
New studies of the 11 beta-hydroxylase and 18-hydroxylase enzymes in the hypertensive form of congenital adrenal hyperplasiaL S Levine, W Rauh, K Gottesdiener, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1993
Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8K M Curnow, L Slutsker, J Vitek, et al.
Biochemistry|February 8, 1994
Natural mutagenesis study of the human steroid 5 alpha-reductase 2 isozymeW C Wigley, J S Prihoda, I Mowszowicz, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1990
Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample studyM Zerah, H Ueshiba, E Wood, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1982
A pilot newborn screening for congenital adrenal hyperplasia in AlaskaS Pang, W Murphey, L S Levine, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1978
Prepubertal diagnosis of steroid 5 alpha-reductase deficiencyP Saenger, A S Goldman, L S Levine, et al.
The International Journal of Pediatric Nephrology|October 1, 1985
Evaluation of percutaneous transluminal renal angioplasty in childhood hypertensionF Fallo, S E Oberfield, L S Levine, et al.
Clinical and Experimental Hypertension. Part A, Theory and Practice|January 1, 1986
Percutaneous transluminal renal angioplasty in the treatment of renovascular hypertension in childrenF Fallo, S E Oberfield, L S Levine, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 7, 1999
Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature reviewM E Damore, P W Speiser, A E Slonim, et al.
Pageof 30