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fludrocortisone and Inborn Errors of Metabolism

fludrocortisone has been researched along with Inborn Errors of Metabolism in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19903 (60.00)18.7374
1990's1 (20.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Birla, S; Jain, R; Jain, V; Sharma, A; Verma, N1
Buchanan, C; Montalto, J; Oakes, S; Pitt, J; Preston, T; Yong, AB1
Hintz, RL; Lee, PD; Patterson, BD; Rosenfeld, RG1
Biglieri, EG; Schambelan, M; Stockigt, JR1
Audi-Parera, L; Bertrand, J; David, M; Loras, B; Roux, H1

Trials

1 trial(s) available for fludrocortisone and Inborn Errors of Metabolism

ArticleYear
[Plasmatic 17-alpha-hydroxyprogesterone in congenital adrenal hyperplasia due to 21 hydroxylase deficiency, treated and untreated].
    Biomedicine / [publiee pour l'A.A.I.C.I.G.], 1974, Volume: 21, Issue:7

    Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adolescent; Adrenal Hyperplasia, Congenital; Adrenocortical Hyperfunction; Adrenocorticotropic Hormone; Binding, Competitive; Blood Proteins; Child; Child, Preschool; Circadian Rhythm; Clinical Trials as Topic; Dexamethasone; Female; Fludrocortisone; Glucocorticoids; Humans; Hydrocortisone; Hydroxyprogesterones; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Pituitary-Adrenal Function Tests; Pituitary-Adrenal System; Protein Binding; Steroid Hydroxylases

1974

Other Studies

4 other study(ies) available for fludrocortisone and Inborn Errors of Metabolism

ArticleYear
Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency.
    Journal of pediatric endocrinology & metabolism : JPEM, 2012, Volume: 25, Issue:11-12

    Topics: 46, XX Disorders of Sex Development; Adolescent; Adrenal Hyperplasia, Congenital; Aromatase; Bone Density; Child Development; Child, Preschool; DNA Mutational Analysis; Estrogen Replacement Therapy; Ethinyl Estradiol; Female; Fludrocortisone; Growth Disorders; Gynecomastia; Humans; Hydrocortisone; Infertility, Male; Insulin Resistance; Male; Metabolism, Inborn Errors; Mutation, Missense; Pedigree; Sexual Maturation

2012
Corticosterone methyl oxidase type II (CMO II) deficiency: biochemical approach to diagnosis.
    Clinical biochemistry, 1994, Volume: 27, Issue:6

    Topics: 18-Hydroxycorticosterone; Aldosterone; Cytochrome P-450 CYP11B2; Diagnosis, Differential; Fludrocortisone; Humans; Hydroxyprogesterones; Infant; Male; Metabolism, Inborn Errors; Mixed Function Oxygenases; Renin

1994
Biochemical diagnosis and management of corticosterone methyl oxidase type II deficiency.
    The Journal of clinical endocrinology and metabolism, 1986, Volume: 62, Issue:1

    Topics: Adrenal Cortex Hormones; Aldosterone; Cytochrome P-450 CYP11B2; Female; Fludrocortisone; Genetic Carrier Screening; Humans; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Mixed Function Oxygenases; Reference Values; Renin

1986
Isolated hypoaldosteronism in adults. A renin-deficiency syndrome.
    The New England journal of medicine, 1972, Sep-21, Volume: 287, Issue:12

    Topics: 17-Hydroxycorticosteroids; Adrenocorticotropic Hormone; Adult; Aged; Aldosterone; Angiotensin II; Diet; Female; Fludrocortisone; Humans; Hyperkalemia; Kidney Function Tests; Male; Metabolism, Inborn Errors; Middle Aged; Potassium; Renin; Sodium; Syndrome

1972