OKA Akira | Division of Basic Molecular Science and Molecular Medicine, School of Medicine, Tokai University

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著作論文

Mental retardation, spasticity, basal ganglia calcification, cerebral white matter lesions, multiple endocrine defects, telangiectasia and atrophic skin : A new syndrome?
Molecular genetic study in Japanese patients with Alexander disease : a novel mutation, R79L
Cardiac ankyrin repeat protein is preferentially induced in atrophic myofibers of congenital myopathy and spinal muscular atrophy
Unilateral occlusion of the middle cerebral artery after varicella-zoster virus infection
Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications
Fukutin expression in mouse non-muscle somatic organs : its relationship to the hypoglycosylation of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
Failure to detect significant association between estrogen receptor-alpha gene polymorphisms and endometriosis in Japanese women
Lack of an association human dioxin detoxification gene polymorphisms with endometriosis in Japanese women : results of a pilot study

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