Wada Hiroko | Division Of Pediatrics Department Of Development And Aging Kobe University School Of Medicine

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著作論文

Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation
Molecular genetics of spinal muscular atrophy : contribution of the NAIP gene to clinical severity
Oligonucleotides against a splicing enhancer sequence led to dystrophin production in muscle cells from a Duchenne muscular dystrophy patient
Vascular involvement in benign infantile mitochondrial myopathy caused by reversible cytochrobe c oxidase dificiency
Severe neonatal nemaline myopathy with delayed maturation of muscle
Preventive effects of dexamethasone on hypoxic-ischemic brain damage in the neonatal rat
Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle
Cardiac Involvement in a Family with Becker Muscular Dystrophy.

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