fludrocortisone has been researched along with Abnormalities, Urogenital in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Bech, AP; Bindels, RJM; Danser, AHJ; de Baaij, JHF; Deinum, J; Steenbergen, EJ; Viering, DHHM; Wetzels, JFM | 1 |
| Bareke, E; Ben Fadel, N; Boycott, KM; Bulman, DE; Carson, N; Daoud, H; Dyment, DA; Fadfel, NB; Feberova, J; Geier, P; Jarinova, O; Khatchadourian, K; Majewski, J; Richer, J; Unrau, J | 1 |
| Gribouval, O; Gubler, MC; Landau, D; Schreiber, R; Shalev, H | 1 |
3 other study(ies) available for fludrocortisone and Abnormalities, Urogenital
| Article | Year |
|---|---|
Functional tests to guide management in an adult with loss of function of type-1 angiotensin II receptor.
Topics: Adult; Angiotensin II; Fludrocortisone; Humans; Hyperkalemia; Kidney Tubules, Proximal; Male; Potassium; Receptor, Angiotensin, Type 1; Receptors, Angiotensin; Renin; Renin-Angiotensin System; Urogenital Abnormalities | 2021 |
Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACE.
Topics: Adult; Anuria; Base Sequence; Female; Fludrocortisone; Frameshift Mutation; Gene Deletion; High-Throughput Nucleotide Sequencing; Humans; Hypotension; Infant, Newborn; Infant, Premature; Kidney Tubules, Proximal; Molecular Sequence Data; Peptidyl-Dipeptidase A; Pregnancy; Treatment Outcome; Urogenital Abnormalities; Vasopressins | 2015 |
Inherited renal tubular dysgenesis may not be universally fatal.
Topics: Anuria; Child, Preschool; Female; Fludrocortisone; Genetic Predisposition to Disease; Heredity; Humans; Hyperkalemia; Hypotension; Kidney Tubules, Proximal; Male; Mutation; Oligohydramnios; Peptidyl-Dipeptidase A; Peritoneal Dialysis; Phenotype; Pregnancy; Treatment Outcome; Urogenital Abnormalities | 2010 |