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Showing results (121-130 of 292) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|December 1, 1992
Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiencyP W Speiser, J Serrat, M I New, et al.
American Journal of Human Genetics|October 1, 1986
Frequent deletion and duplication of the steroid 21-hydroxylase genesJ W Werkmeister, M I New, B Dupont, et al.
Human Genetics|January 1, 1981
The biochemical basis for genotyping 21-hydroxylase deficiencyM I New, B Dupont, M S Pollack, et al.
Metabolism: Clinical and Experimental|May 1, 1972
Androgen production in boys with sexual precocity and congenital adrenal hyperplasiaL S Levine, M I New, P Pitt, et al.
Metabolism: Clinical and Experimental|July 1, 1993
Investigation of the mechanism of hypertension in apparent mineralocorticoid excessP W Speiser, L M Riddick, K Martin, et al.
Pediatric Neurology|July 1, 1986
Empty sella syndrome in childhoodR Nass, M Engel, E Stoner, et al.
The New England Journal of Medicine|May 21, 1987
Hirsutism, polycystic ovarian disease, and ovarian 17-ketosteroid reductase deficiencyS Y Pang, B Softness, W J Sweeney, et al.
The Journal of Pediatrics|January 1, 1976
Letter: Somatomedin in cerebral gigantismP Saenger, L S Levine, E Wiedemann, et al.
Prenatal Diagnosis|March 4, 1998
Normal external genitalia in a female with classical congenital adrenal hyperplasia who was not treated during embryogenesisN Quercia, D Chitayat, R Babul-Hirji, et al.
Acta Paediatrica Japonica : Overseas Edition|January 1, 1988
Growth and final height in classical and nonclassical 21-hydroxylase deficiencyM I New, J M Gertner, P W Speiser, et al.
Pageof 30

Showing results (121-130 of 292) with videos related to

Sort By:
Pageof 30
The Journal of Clinical Endocrinology and Metabolism|December 1, 1992
Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiencyP W Speiser, J Serrat, M I New, et al.
American Journal of Human Genetics|October 1, 1986
Frequent deletion and duplication of the steroid 21-hydroxylase genesJ W Werkmeister, M I New, B Dupont, et al.
Human Genetics|January 1, 1981
The biochemical basis for genotyping 21-hydroxylase deficiencyM I New, B Dupont, M S Pollack, et al.
Metabolism: Clinical and Experimental|May 1, 1972
Androgen production in boys with sexual precocity and congenital adrenal hyperplasiaL S Levine, M I New, P Pitt, et al.
Metabolism: Clinical and Experimental|July 1, 1993
Investigation of the mechanism of hypertension in apparent mineralocorticoid excessP W Speiser, L M Riddick, K Martin, et al.
Pediatric Neurology|July 1, 1986
Empty sella syndrome in childhoodR Nass, M Engel, E Stoner, et al.
The New England Journal of Medicine|May 21, 1987
Hirsutism, polycystic ovarian disease, and ovarian 17-ketosteroid reductase deficiencyS Y Pang, B Softness, W J Sweeney, et al.
The Journal of Pediatrics|January 1, 1976
Letter: Somatomedin in cerebral gigantismP Saenger, L S Levine, E Wiedemann, et al.
Prenatal Diagnosis|March 4, 1998
Normal external genitalia in a female with classical congenital adrenal hyperplasia who was not treated during embryogenesisN Quercia, D Chitayat, R Babul-Hirji, et al.
Acta Paediatrica Japonica : Overseas Edition|January 1, 1988
Growth and final height in classical and nonclassical 21-hydroxylase deficiencyM I New, J M Gertner, P W Speiser, et al.
Pageof 30