theophylline has been researched along with Hyperoxaluria, Primary in 1 studies
Hyperoxaluria, Primary: A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Pospekhova, GP | 1 |
| Kaiukov, IG | 1 |
| Sinitsina, TM | 1 |
| Razorenova, TS | 1 |
1 other study available for theophylline and Hyperoxaluria, Primary
| Article | Year |
|---|---|
[The relationships between the broncholytic and diuretic effects of theophylline in patients with obstructive lung diseases combined with oxalosis].
Topics: Bronchodilator Agents; Diuresis; Diuretics; Drug Evaluation; Female; Humans; Hyperoxaluria, Primary; | 1997 |