Ichizo Nishino
National Institute of Neuroscience, National Center of Neurology and Psychiatry
392 papers found
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Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy
Download from www.ncbi.nlm.nih.govLimb-girdle muscular dystrophy type 2I is not rare in Taiwan
Download from www.researchgate.netThink worldwide: Hereditary myopathy with early respiratory failure (HMERF) may not be rare
Download from www.researchgate.netRapidly progressive scoliosis and respiratory deterioration in Ullrich congenital muscular dystrophy
Download from www.researchgate.netCell stress molecules in the skeletal muscle of GNE myopathy
Download from dx.doi.orgLimb-girdle Muscular Dystrophy Type 2A with Mutation in CAPN3: The First Report in Taiwan
Download from doi.orgDaily or alternative, that is the question: Steroid therapy for Duchenne muscular dystrophy patients
Download from www.researchgate.netVMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy.
Download from link.springer.comDNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions.
Download from www.researchgate.netAn advanced case of myopathy and dementia with a new mutation in the valosin-containing protein gene
Download from www.jstage.jst.go.jpNew congenital muscular dystrophy due to CHKB mutations
Download from www.researchgate.net[A case of systemic lupus erythematosus predominantly presenting with myositis at onset]
Download from www.jstage.jst.go.jpMissing publications? Search for publications with a matching author name.