Supporting Families. Saving Lives.
MMRL invites participation and collaboration in research projects particularly in individuals, or preferably, large families with any of the following: Brugada Syndrome, Spontaneous Brugada ECG phenotype, Brugada phenotype unmasked or induced by sodium channel blockers, hormonal imbalances, pheochromocytoma antidepressant or other drugs, hyponatremia or other electrolyte imbalances, alcohol, vagotonic agents or vagal maneuvers (including full stomach), Familial Atrial Fibrillation, Catecholamine-sensitive VT, Non-ischemia-related VT/VF occurring in young individuals, Post-MI QT prolongation and Torsade de Pointes, Progressive Conduction Disease, Sudden death in infants and children (including SIDS), Acquired Long QT Syndrome and Short QT Syndrome.
For more information on participating in research, call toll-free 1-888-888-MMRL or via their website at: http://www.mmrl.edu/information.asp