Search Results21-28 of  28

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  • Ishikawa Kinya ID: 9000258060190

    Department of Neurology and Neurological Science, Tokyo Medical and Dental University (2012 from CiNii)

    Articles in CiNii:1

    • Optic nerve swelling and gadolinium contrast enhancement on magnetic resonance imaging in the subacute stage of Leber's hereditary optic neuropathy: A case report (2012)
  • Ishikawa Kinya ID: 9000258061379

    Department of Neurology and Neurological Science, Graduate School, Tokyo Medical and Dental University (2014 from CiNii)

    Articles in CiNii:1

    • Clinical features and MRI findings in spinocerebellar ataxia type 31 (SCA31) comparing with spinocerebellar ataxia type 6 (SCA6) (2014)
  • Ishikawa Kinya ID: 9000317557758

    Articles in CiNii:1

    • Rare frequency of downbeat positioning nystagmus in spinocerebellar ataxia type 31 (2015)
  • Ishikawa Kinya ID: 9000345423418

    Department of Neurology and Neurological Science, Graduate School, Tokyo Medical and Dental University, Yushima 1-5-45, Bunkyo-ku 113-8519, Tokyo, Japan. (2008 from CiNii)

    Articles in CiNii:1

    • Analyses of copy number and mRNA expression level of the α-synuclein gene in multiple system atrophy (2008)
  • Ishikawa Kinya ID: 9000381496745

    Department of Neurology and Neurological Science, Tokyo Medical and Dental University, Japan (2018 from CiNii)

    Articles in CiNii:1

    • Spinocerebellar Ataxia Type 31 with Blepharospasm (2018)
  • Ishikawa Kinya ID: 9000396105100

    Department of Neurology and Neurological Science, Tokyo Medical and Dental University, Japan (2018 from CiNii)

    Articles in CiNii:1

    • Spinocerebellar Ataxia Type 31 with Blepharospasm (2018)
  • Ishikawa Kinya ID: 9000399361389

    東京医科歯科大学医学部附属病院長寿・健康人生推進センター (2018 from CiNii)

    Articles in CiNii:1

    • 脊髄小脳失調症の治療の進歩 (2018)
  • Ishikawa Kinya ID: 9000402808107

    The Center for Personalized Medicine for Healthy Aging, Tokyo Medical and Dental University (2019 from CiNii)

    Articles in CiNii:1

    • SCA6 : cerebellar ataxia with characteristic neuro-otological features (2019)
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