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9-(2-hydroxy-3-nonyl)adenine and Brugada Syndrome

9-(2-hydroxy-3-nonyl)adenine has been researched along with Brugada Syndrome in 1 studies

9-(2-hydroxy-3-nonyl)adenine: specific inhibitor of adenosine deaminase

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.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kommajosyula, SP1
Randall, ME1
Faingold, CL1

Other Studies

1 other study available for 9-(2-hydroxy-3-nonyl)adenine and Brugada Syndrome

ArticleYear
Inhibition of adenosine metabolism induces changes in post-ictal depression, respiration, and mortality in genetically epilepsy prone rats.
    Epilepsy research, 2016, Volume: 119

    Topics: Adenine; Adenosine; Animals; Blood Gas Analysis; Brugada Syndrome; Disease Models, Animal; Enzyme In

2016