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Sodium channel mutations in acetazolamide-responsive myotonia congenital. Identifying the lowest effective dose of acetazolamide for the prophylaxis of acute. Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive. Med Int Mex 2008;24(1):69-75 Caso clínico Parálisis periódica familiar. Hypokalemic periodic paralysis presents in 1 of each 100,000; in addition it affects more. Acetazolamide treatment of hypokalemic paralysis. Alterations in this channel produce flaccid paralysis, arrhythmias, impaired skeletal. correlation and therapeutic rationale in hyperkalemic periodic paralysis. Amiodarone and acetazolamide for the treatment of genetically. Molecular diagnosis of hyperkalemic periodic paralysis (SCN4A gene); Genetica AG. Molecular diagnosis of Acetazolamide-Responsive Congenital Myotonia. mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. Neurology 1994; 44:1500-1503. 14.
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