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Showing results (191-200 of 292) with videos related to

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Recent Progress in Hormone Research|January 1, 1994
Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridizationP W Speiser, P C White, J Dupont, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiencyA B Mercado, R C Wilson, K C Cheng, et al.
Therapeutic Drug Monitoring|January 1, 1986
Microfilter paper method for antipyrine determination in whole blood by high pressure liquid chromatographyS Loche, A B Rifkind, E Stoner, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 1995
Molecular basis of human 3 beta-hydroxysteroid dehydrogenase deficiencyJ Simard, E Rheaume, F Mebarki, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1978
Serum androgens as a continuing index of adequacy of treatment of congenital adrenal hyperplasiaS Korth-Schutz, R Virdis, P Saenger, et al.
Journal of Child Neurology|April 1, 1997
Magnetic resonance imaging in the congenital adrenal hyperplasia population: increased frequency of white-matter abnormalities and temporal lobe atrophyR Nass, L Heier, T Moshang, et al.
Clinical Endocrinology|January 1, 1986
Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect?E Stoner, J Dimartino-Nardi, U Kuhnle, et al.
Pediatric Research|September 1, 1980
Aldosterone response to prolonged ACTH infusion in juvenile hypertensionW Rauh, K Gottesdiener, D Chow, et al.
The Journal of Pediatrics|October 1, 1979
Use of the oral angiotensin I--converting enzyme inhibitor (captopril) in childhood malignant hypertensionS E Oberfield, D B Case, L S Levine, et al.
Human Genetics|April 1, 1994
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blotP W Speiser, P C White, J Dupont, et al.
Pageof 30

Showing results (191-200 of 292) with videos related to

Sort By:
Pageof 30
Recent Progress in Hormone Research|January 1, 1994
Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridizationP W Speiser, P C White, J Dupont, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiencyA B Mercado, R C Wilson, K C Cheng, et al.
Therapeutic Drug Monitoring|January 1, 1986
Microfilter paper method for antipyrine determination in whole blood by high pressure liquid chromatographyS Loche, A B Rifkind, E Stoner, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 1995
Molecular basis of human 3 beta-hydroxysteroid dehydrogenase deficiencyJ Simard, E Rheaume, F Mebarki, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1978
Serum androgens as a continuing index of adequacy of treatment of congenital adrenal hyperplasiaS Korth-Schutz, R Virdis, P Saenger, et al.
Journal of Child Neurology|April 1, 1997
Magnetic resonance imaging in the congenital adrenal hyperplasia population: increased frequency of white-matter abnormalities and temporal lobe atrophyR Nass, L Heier, T Moshang, et al.
Clinical Endocrinology|January 1, 1986
Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect?E Stoner, J Dimartino-Nardi, U Kuhnle, et al.
Pediatric Research|September 1, 1980
Aldosterone response to prolonged ACTH infusion in juvenile hypertensionW Rauh, K Gottesdiener, D Chow, et al.
The Journal of Pediatrics|October 1, 1979
Use of the oral angiotensin I--converting enzyme inhibitor (captopril) in childhood malignant hypertensionS E Oberfield, D B Case, L S Levine, et al.
Human Genetics|April 1, 1994
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blotP W Speiser, P C White, J Dupont, et al.
Pageof 30