fludrocortisone has been researched along with Inborn Errors of Metabolism in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (60.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Birla, S; Jain, R; Jain, V; Sharma, A; Verma, N | 1 |
Buchanan, C; Montalto, J; Oakes, S; Pitt, J; Preston, T; Yong, AB | 1 |
Hintz, RL; Lee, PD; Patterson, BD; Rosenfeld, RG | 1 |
Biglieri, EG; Schambelan, M; Stockigt, JR | 1 |
Audi-Parera, L; Bertrand, J; David, M; Loras, B; Roux, H | 1 |
1 trial(s) available for fludrocortisone and Inborn Errors of Metabolism
Article | Year |
---|---|
[Plasmatic 17-alpha-hydroxyprogesterone in congenital adrenal hyperplasia due to 21 hydroxylase deficiency, treated and untreated].
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 |
4 other study(ies) available for fludrocortisone and Inborn Errors of Metabolism
Article | Year |
---|---|
Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency.
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.
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.
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.
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 |