Page last updated: 2024-08-26

17-alpha-hydroxypregnenolone and Inborn Errors of Metabolism

17-alpha-hydroxypregnenolone has been researched along with Inborn Errors of Metabolism in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19904 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
BIRCHALL, K; CATHRO, DM; FORSYTH, CC; MITCHELL, FL1
Curtius, HC; New, MI; Prader, A; Völlmin, JA; Zachmann, M1
Gregorová, I; Horký, K; Kuchel, O; Stárka, L1
Hamilton, W; Prader, A; Völlmin, JA; Zachmann, M1

Trials

1 trial(s) available for 17-alpha-hydroxypregnenolone and Inborn Errors of Metabolism

ArticleYear
Effect of aminoglutethimide on urinary steroid excretion in patients with congenital adrenal hyperplasia due to incomplete 21-hydroxylase deficiency.
    Metabolism: clinical and experimental, 1972, Volume: 21, Issue:4

    Topics: 17-alpha-Hydroxypregnenolone; 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Glands; Adrenal Hyperplasia, Congenital; Adrenalectomy; Adrenocorticotropic Hormone; Adult; Aminoglutethimide; Androsterone; Aniline Compounds; Anticonvulsants; Chemistry, Clinical; Clinical Trials as Topic; Dehydroepiandrosterone; Depression, Chemical; Dexamethasone; Etiocholanolone; Female; Humans; Metabolism, Inborn Errors; Metyrapone; Mixed Function Oxygenases; Pregnanetriol; Pyridones

1972

Other Studies

3 other study(ies) available for 17-alpha-hydroxypregnenolone and Inborn Errors of Metabolism

ArticleYear
3BETA: 21-DIHYDROXYPREGN-5-ENE-20-ONE IN URINE OF NORMAL NEWBORN INFANTS AND IN THIRD DAY URINE OF CHILD WITH DEFICIENCY OF 3BETA-HYDROXYSTEROID-DEHYDROGENASE.
    Archives of disease in childhood, 1965, Volume: 40

    Topics: 17-alpha-Hydroxypregnenolone; 17-Hydroxysteroid Dehydrogenases; Adrenal Cortex Hormones; Female; Humans; Hydroxysteroid Dehydrogenases; Hydroxysteroids; Infant, Newborn; Infant, Premature; Metabolism; Metabolism, Inborn Errors; Pregnancy; Pregnancy in Diabetics; Pregnenolone; Urine

1965
Congenital adrenal hyperplasia due to deficiency of 11 -hydroxylation of 17 -hydroxylated steroids.
    The Journal of clinical endocrinology and metabolism, 1971, Volume: 33, Issue:3

    Topics: 17-alpha-Hydroxypregnenolone; 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Glands; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Chromatography, Gas; Female; Humans; Hydroxysteroid Dehydrogenases; Hyperplasia; Infant; Metabolism, Inborn Errors; Mixed Function Oxygenases; Pregnanediol; Pregnanetriol; Secretory Rate

1971
Steroid 17,20-desmolase deficiency: a new cause of male pseudohermaphroditism.
    Clinical endocrinology, 1972, Volume: 1, Issue:4

    Topics: 17-alpha-Hydroxypregnenolone; Adolescent; Adrenal Glands; Adrenocorticotropic Hormone; Androgens; Child, Preschool; Chorionic Gonadotropin; Disorders of Sex Development; Female; Humans; Infant; Lyases; Male; Metabolism, Inborn Errors; Pedigree; Pregnanes; Pregnenes; Testis

1972