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Showing results (141-150 of 292) with videos related to

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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 Pediatrics|July 1, 1974
Letter: Growth with absent growth hormone by radioimmunoassayP Saenger, L S Levine, E Wiedemann, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1974
An unusual case of Cushing's syndrome, hilus cell tumor and polycystic ovariesS Korth-Schutz, L S Levine, I R Merkatz, 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.
American Journal of Diseases of Children (1960)|September 1, 1971
Cushing's syndrome in infancy. A case complicated by monilial endocarditisR Giombetti, J W Hagstrom, S Landey, 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.
Fertility and Sterility|July 1, 1992
Nonclassical 3 beta-hydroxysteroid dehydrogenase deficiency: a review of our experience with 25 female patientsP Schram, M Zerah, P Mani, 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.
Pageof 30

Showing results (141-150 of 292) with videos related to

Sort By:
Pageof 30
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 Pediatrics|July 1, 1974
Letter: Growth with absent growth hormone by radioimmunoassayP Saenger, L S Levine, E Wiedemann, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1974
An unusual case of Cushing's syndrome, hilus cell tumor and polycystic ovariesS Korth-Schutz, L S Levine, I R Merkatz, 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.
American Journal of Diseases of Children (1960)|September 1, 1971
Cushing's syndrome in infancy. A case complicated by monilial endocarditisR Giombetti, J W Hagstrom, S Landey, 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.
Fertility and Sterility|July 1, 1992
Nonclassical 3 beta-hydroxysteroid dehydrogenase deficiency: a review of our experience with 25 female patientsP Schram, M Zerah, P Mani, 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.
Pageof 30