4-aminopyridine has been researched along with Granulomatous Disease, Chronic in 1 studies
Granulomatous Disease, Chronic: A defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation. When chronic granulomatous disease is caused by mutations in the CYBB gene, the condition is inherited in an X-linked recessive pattern. When chronic granulomatous disease is caused by CYBA, NCF1, NCF2, or NCF4 gene mutations, the condition is inherited in an autosomal recessive pattern.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fu, XW | 1 |
| Wang, D | 1 |
| Nurse, CA | 1 |
| Dinauer, MC | 1 |
| Cutz, E | 1 |
1 other study available for 4-aminopyridine and Granulomatous Disease, Chronic
| Article | Year |
|---|---|
NADPH oxidase is an O2 sensor in airway chemoreceptors: evidence from K+ current modulation in wild-type and oxidase-deficient mice.
Topics: 4-Aminopyridine; Animals; Base Sequence; Cell Hypoxia; Chemoreceptor Cells; DNA Primers; Granulomato | 2000 |