Notch3 遺伝子に新たなミスセンス変異をみとめた CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) の1例 : 禿頭と腰椎椎間板ヘルニアの合併について  [in Japanese] Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene : association with alopecia and lumbar herniated disk  [in Japanese]

Author(s)

    • 安田 雄 YASUDA Takeshi
    • 川崎医科大学神経内科 Division of Neurology, Department of Internal Medicine, Kawasaki Medical School
    • 小鳥居 聡 [他] KOTORII Satoshi
    • 国立精神・神経センター神経研究所疾病研究第6部 Department of Demyelinating Disease and Aging, National Institute of Neuroscience, National Center of Neurology and Psychiatry
    • 高橋 慶吉 TAKAHASHI Keikichi
    • 国立精神・神経センター神経研究所疾病研究第6部 Department of Demyelinating Disease and Aging, National Institute of Neuroscience, National Center of Neurology and Psychiatry
    • 田平 武 TABIRA Takeshi
    • 国立精神・神経センター神経研究所疾病研究第6部 Department of Demyelinating Disease and Aging, National Institute of Neuroscience, National Center of Neurology and Psychiatry

Journal

  • 臨床神経学

    臨床神経学 41(2), 144-146, 2001-02-01

    日本神経学会

References:  10

Cited by:  4

Codes

  • NII Article ID (NAID)
    10008444914
  • NII NACSIS-CAT ID (NCID)
    AN00253207
  • Text Lang
    JPN
  • Article Type
    Journal Article
  • ISSN
    0009918X
  • NDL Article ID
    025974079
  • NDL Call No.
    Z19-298
  • Data Source
    CJP  CJPref  NDL 
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