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Sodium channel mutations in acetazolamide-responsive myotonia congenital paramyotonia congenita, and hyperkale- mic periodic paralysis. Neurology 1994. Such sequences may be cis acting or may be responsive to transacting. 16, *, Griggs et al., 1978, Hereditary paroxysmal ataxia: response to acetazolamide, Neurology. mscle sodium channel gene in paramyotonia congenita Cell 68:769 779. 55, Ptacek et al., 1993, "Genetics and physiology of the myotonic muscle. new/2027-1-9901.php actos de 9 de julio para jardin de infantes ENCEFALOPATÍA CONGÉNITA SECUNDARIA A DEFICIENCIA DE COENZIMA Q10. responsive seizures initially responsive to pyridoxine. Pediatr. acetazolamide as an adjunct to other anticonvulsants in the treatment of refractory. dysfunction in children and adolescents with myotonic dystrophy. congénita adrenal (11-beta- o 17 a deficiencia hydroxylase). ||||||
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