Search Results1-7 of  7

  • KAWARAI Toshitaka ID: 9000016672480

    Articles in CiNii:6

    • A case of late onset CMT2 associated with novel missense mutation in the MPZ gene (2008)
    • Brachial plexus injury following open heart surgery successfully treated with methylpredonisolone pulse therapy : patient report (2008)
    • Clinical characteristics of X-linked dystonia-parkinsonism (2011)
  • KAWARAI Toshitaka ID: 9000016850370

    Department of Neurology, Hyogo Brain and Heart Center at Himeji (2010 from CiNii)

    Articles in CiNii:3

    • Elderly case of Dieulafoy's lesion in the jejunum presenting with repeated hemorrhagic shocks (2010)
    • Elderly case of prolonged hypoglycemic coma presenting with reversible magnetic resonance imaging changes (2010)
    • Re-evaluation of Clinical Features and Risk Factors of Acute Ischemic Stroke in Japanese Longevity Society (2009)
  • Kawarai Toshitaka ID: 9000239601977

    Articles in CiNii:1

    • Re-evaluation of Clinical Features and Risk Factors of Acute Ischemic Stroke in Japanese Longevity Society (2009)
  • Kawarai Toshitaka ID: 9000258060718

    Department of Clinical Neuroscience, Institute of Health Biosciences, The University of Tokushima Graduate School (2013 from CiNii)

    Articles in CiNii:1

    • Pathomechanisms of motor neuron death by mutant TFG (2013)
  • Kawarai Toshitaka ID: 9000258061002

    Department of Clinical Neuroscience Institute of Health Biosciences, Graduate School of Medicine, University of Tokushima (2013 from CiNii)

    Articles in CiNii:1

    • Dystonia genes and elucidation of their roles in dystonia pathogenesis (2013)
  • Kawarai Toshitaka ID: 9000344128661

    Articles in CiNii:1

    • Proteasome impairment in neural cells derived from HMSN-P patient iPSCs (2017)
  • Kawarai Toshitaka ID: 9000368417761

    Department of Clinical Neuroscience, Institute of Biomedical Sciences, Tokushima University Graduate School (2017 from CiNii)

    Articles in CiNii:1

    • MR Spectroscopy in Patients with Hereditary Diffuse Leukoencephalopathy with Spheroids and Asymptomatic Carriers of Colony-stimulating Factor 1 Receptor Mutation (2017)
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