Compounds > pregnenolone
Page last updated: 2024-08-20

pregnenolone and Hypokalemia

pregnenolone has been researched along with Hypokalemia in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19904 (80.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Auchus, RJ; Costa-Santos, M; Kater, CE1
Takeda, R1
Brough, AJ; Camacho, AM; Kowarski, A; Migeon, CJ1
Hiwada, K; Koto, K; Kumagai, A; Morimoto, Y; Nanahoshi, M; Okano, K; Uda, H; Yamamura, Y; Yamane, G; Yano, S1
Bricaire, H; Corvol, P; Laudat, P; Legrand, JC; Lemmer, M; Luton, JP; Turpin, G1

Reviews

1 review(s) available for pregnenolone and Hypokalemia

ArticleYear
[Review on internal medicine, 1984. Electrolyte disturbance. II-2. Mineralocorticoids and potassium imbalance].
    Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 1985, Volume: 74, Issue:6

    Topics: Adult; Aldosterone; Bartter Syndrome; Chlorides; Desoxycorticosterone; Female; Humans; Hypokalemia; Male; Potassium; Pregnenolone

1985

Other Studies

4 other study(ies) available for pregnenolone and Hypokalemia

ArticleYear
Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency.
    The Journal of clinical endocrinology and metabolism, 2004, Volume: 89, Issue:1

    Topics: Adolescent; Adrenal Hyperplasia, Congenital; Adult; Animals; Brazil; Cell Line; Child; Chlorocebus aethiops; COS Cells; DNA Mutational Analysis; Female; Founder Effect; Gene Expression; Genotype; Gonadal Steroid Hormones; Humans; Hypertension; Hypokalemia; Male; Models, Molecular; Molecular Structure; Mutation; Mutation, Missense; Phenotype; Polymerase Chain Reaction; Portugal; Pregnenolone; Puberty; Saccharomyces cerevisiae; Spain; Steroid 17-alpha-Hydroxylase; Transfection; Tritium

2004
Congenital adrenal hyperplasia due to a deficiency of one of the enzymes involved in the biosynthesis of pregnenolone.
    The Journal of clinical endocrinology and metabolism, 1968, Volume: 28, Issue:2

    Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Glands; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Desoxycorticosterone; Disorders of Sex Development; Humans; Hydrocortisone; Hydroxysteroid Dehydrogenases; Hypokalemia; Hyponatremia; Infant; Male; Metabolism, Inborn Errors; Mixed Function Oxygenases; Pregnanediol; Pregnanetriol; Pregnenolone; Secretory Rate; Urine; Water-Electrolyte Balance

1968
Cushing's syndrome caused by malignant tumor in the scrotum: clinical, pathologic and biochemical studies.
    The Journal of clinical endocrinology and metabolism, 1971, Volume: 32, Issue:2

    Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Rest Tumor; Adrenocorticotropic Hormone; Androstanes; Autopsy; Chromatography; Corticosterone; Cushing Syndrome; Dehydroepiandrosterone; Dexamethasone; Edema; Humans; Hydrocortisone; Hypokalemia; Male; Metyrapone; Middle Aged; Mixed Function Oxygenases; Neoplasm Metastasis; Pregnanes; Pregnenolone; Progesterone; Retroperitoneal Neoplasms; Scrotum; Tritium

1971
A new male pseudo-hermaphroditism associated with hypertension due to a block of 17 -hydroxylation.
    The Journal of clinical endocrinology and metabolism, 1972, Volume: 35, Issue:1

    Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adult; Aldosterone; Corticosterone; Desoxycorticosterone; Dexamethasone; Disorders of Sex Development; Estrogens; Humans; Hydroxycorticosteroids; Hypertension; Hypokalemia; Karyotyping; Male; Metabolic Diseases; Mixed Function Oxygenases; Pregnanediol; Pregnenolone; Progesterone

1972