chymosin has been researched along with fludrocortisone in 1 studies
| Studies (chymosin) | Trials (chymosin) | Recent Studies (post-2010) (chymosin) | Studies (fludrocortisone) | Trials (fludrocortisone) | Recent Studies (post-2010) (fludrocortisone) |
|---|---|---|---|---|---|
| 1,018 | 6 | 258 | 1,677 | 120 | 302 |
| 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| 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 |
1 other study(ies) available for chymosin and fludrocortisone
| Article | Year |
|---|---|
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 |