memantine has been researched along with Brugada Syndrome in 1 studies
Brugada Syndrome: An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK; high risk of VENTRICULAR TACHYCARDIA; or VENTRICULAR FIBRILLATION; SYNCOPAL EPISODE; and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit.
| 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 |
|---|---|
| Takehara, H | 1 |
| Suzuki, Y | 1 |
| Someya, T | 1 |
1 other study available for memantine and Brugada Syndrome
| Article | Year |
|---|---|
QT prolongation associated with memantine in Alzheimer's disease.
Topics: Aged; Alzheimer Disease; Arrhythmias, Cardiac; Brugada Syndrome; Cardiac Conduction System Disease; | 2015 |