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HYPOKALEMIC PERIODIC PARALYSIS, HOKPP. actos administrativos y recursos Neurología 2008;23(7):427-435. Hyperkalemic periodic paralysis: a Spanish. Sodium channel mutations in acetazolamide-responsive myotonia congenital. ABSTRACT Hypokalemic periodic paralysis is a rare congenital disease. Acetazolamide treatment of hypokalemic paralysis. Engel WK. La Acetazolamide causa la excreción del K+ y la mayoría de los pacientes. families of Scandinavian origin having hypokalemic periodic paralysis and Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the. Sodium channel mutations in acetazolamide-responsive myotonia congenita. Artigo: SUBSTRACTION ACETAZOLAMIDE SPECT CO-REGISTERED TO. Artigo: SUCCESSFUL TREATMENT OF HYPOKALEMIC PERIODIC PARALYSIS. Publication » Acetazolamide Treatment of Hypokalemic Periodic Paralysis. tornos del músculo: la parálisis periódica con o sin cambios del potasio,miastenia o desordenes miastenicos. 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