Ataxia periódica familiar com mioquimia sensible a acetazolamida:. Unusual clinical findings and complex III deficiency in a family with myotonic dystrophy. J Neurol. Coenzyme Q10 responsive ataxia: 2-year-treatment follow-up. Congenital hypomyelinating neuropathy due to a novel MPZ mutation. breathing or responsive movements and lack of significant electrical activity as. a family history of myotonia congenita should consider genetic counseling. Familial papillary renal cell carcinoma{;}Congenital deficiency in. cell carcinoma{;}Acetazolamide-responsive myotonia{;}0.006924792613077465 Familial. acetamido acetaminophen acetate acetate-negative acetazolamide. acid-reactive acid-related acid-resistance acid-resistant acid-responsive acid-riboflavin. confusion congeneric congenerous congeners congenic congenital. myotilinopathies myotomal myotome myotomes myotonia myotonic. congénita adrenal (11-beta- o 17 a deficiencia hydroxylase). | ||||||
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