Search Results1-20 of  83

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  • Nishino Ichizo ID: 9000403273894

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Japan (2020 from CiNii)

    Articles in CiNii:1

    • Anti-signal Recognition Particle Antibody-positive Necrotizing Myopathy with Secondary Cardiomyopathy: The First Myocardial Biopsy- and Multimodal Imaging-proven Case (2020)
  • Nishino Ichizo ID: 9000404094362

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2019 from CiNii)

    Articles in CiNii:1

    • Continuous hyperCKemia without calf muscle hypertrophy associated with S1 radiculopathy (2019)
  • Nishino Ichizo ID: 9000326637745

    Articles in CiNii:1

    • Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing : validation analysis of DMD mutations (2016)
  • Nishino Ichizo ID: 9000356596748

    Articles in CiNii:1

    • TBCD may be a causal gene in progressive neurodegenerative encephalopathy with atypical infantile spinal muscular atrophy (2017)
  • Nishino Ichizo ID: 9000356664791

    Articles in CiNii:1

    • A novel mutation in the proteolytic domain of LONP1 causes atypical CODAS syndrome (2017)
  • Nishino Ichizo ID: 9000389001951

    Articles in CiNii:1

    • Genetic and functional analysis of the RYR1 mutation p.Thr84Met revealed a susceptibility to malignant hyperthermia (2018)
  • NISHINO ICHIZO ID: 9000001760414

    National Center of Neurology and Psychiatry (2006 from CiNii)

    Articles in CiNii:1

    • Expression of Myoferlin in Skeletal Muscles of Patients with Dysferlinopathy (2006)
  • NISHINO ICHIZO ID: 9000014168879

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2008 from CiNii)

    Articles in CiNii:1

    • Malignant hyperthermia susceptibility diagnosed with a family-specific ryanodine receptor gene type 1 mutation (2008)
  • NISHINO ICHIZO ID: 9000018243247

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP) (2009 from CiNii)

    Articles in CiNii:1

    • Functional analysis of ryanodine receptor type 1 p.R2508C mutation in exon 47 (2009)
  • NISHINO Ichizo ID: 1000000332388

    Articles in CiNii:50

    • Two Sibling Patients with Non-Fukuyama Type Congenital Muscular Dystrophy with Low Serum Selenium Levels -Therapeutic Effects of Oral Selenium Administration- (2000)
    • X-linked Recessive Myotubular Myopathy with a Splice-Site Mutation in the Myotubularin Gene (1998)
    • 心筋症とミオパチー (2001)
  • NISHINO Ichizo ID: 9000001669250

    Department of Neuromuscular disorders, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2005 from CiNii)

    Articles in CiNii:1

    • Early onset distal muscular dystrophy with normal dysferlin expression (2005)
  • NISHINO Ichizo ID: 9000001774076

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2006 from CiNii)

    Articles in CiNii:1

    • Humanin expression in skeletal muscles of patients with chronic progressive external ophthalmoplegia (2006)
  • NISHINO Ichizo ID: 9000002060363

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2006 from CiNii)

    Articles in CiNii:1

    • Distal myopathy with rimmed vacuoles in a case of opercular syndrome (2006)
  • NISHINO Ichizo ID: 9000002060960

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2006 from CiNii)

    Articles in CiNii:1

    • A case of congenital neuromuscular disease with uniform type 1 fibers (2006)
  • NISHINO Ichizo ID: 9000006861001

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2009 from CiNii)

    Articles in CiNii:10

    • The First Molecular Evidence That Autophagy Relates Rimmed Vacuole Formation in Chloroquine Myopathy (2002)
    • Expression of ARPP-16/19 in Rat Denervated Skeletal Muscle (2003)
    • Subcellular Localization of Fukutin and Fukutin-Related Protein in Muscle Cells (2004)
  • NISHINO Ichizo ID: 9000006884754

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2009 from CiNii)

    Articles in CiNii:1

    • Novel LAMP-2 Mutation in a Family With Danon Disease Presenting With Hypertrophic Cardiomyopathy (2009)
  • NISHINO Ichizo ID: 9000014169678

    Department of Neuromuscular Research, National Institute of Neuroscience, NCNP (2010 from CiNii)

    Articles in CiNii:2

    • Familial reducing body myopathy (2007)
    • Central nervous system and muscle involvement in an adolescent patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (2010)
  • NISHINO Ichizo ID: 9000018467678

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2010 from CiNii)

    Articles in CiNii:1

    • Bilateral occipital cortical dysplasia and white matter T2 hyperintensity with mild non-specific myopathy : Two sibling cases (2010)
  • NISHINO Ichizo ID: 9000018776737

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2011 from CiNii)

    Articles in CiNii:1

    • Myopathy and neurogenic muscular atrophy in unexpected cardiopulmonary arrest (2011)
  • NISHINO Ichizo ID: 9000019185863

    Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2012 from CiNii)

    Articles in CiNii:1

    • Myotonic dystrophy type 2 is rare in the Japanese population (2012)
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