fludrocortisone has been researched along with Hyperuricemia in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Choi, Y; Kang, HG; Lee, BH | 1 |
| Adams, JN; Bleyer, AJ; Cornell, LD; Elleder, M; Hart, PS; Hart, TC; Haws, R; Hodanová, K; Hulková, H; Kapp, K; Kmoch, S; Sikora, J; Sovová, J; Vyletal, P; Zivná, M; Zivný, J | 1 |
2 other study(ies) available for fludrocortisone and Hyperuricemia
| Article | Year |
|---|---|
Hyporeninemic hypoaldosteronism in a child with chronic kidney disease--is this condition renoprotective?
Topics: Anti-Inflammatory Agents; Combined Modality Therapy; Drug Therapy, Combination; Fludrocortisone; Humans; Hyperkalemia; Hyperuricemia; Hypoaldosteronism; Infant; Kidney Failure, Chronic; Male; Renin-Angiotensin System | 2009 |
Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone.
Topics: Adult; Amino Acid Sequence; Anemia; Base Sequence; Biopsy; Blood Pressure; Cell Line; Child; Chronic Disease; Chymosin; Cytoplasm; DNA Mutational Analysis; Endoplasmic Reticulum; Enzyme Precursors; Female; Fludrocortisone; Genes, Dominant; Genetic Predisposition to Disease; Glomerular Filtration Rate; Glycosylation; Heterozygote; Humans; Hyperuricemia; Hypoaldosteronism; Kidney Concentrating Ability; Kidney Diseases; Male; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Polyuria; Protein Processing, Post-Translational; Protein Sorting Signals; Protein Transport; Renin; Transfection; Treatment Outcome | 2010 |