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Japanese

Familial unusual encephalopathy of Binswanger's type without hypertension Susumu MAEDA 1 , Susumu YOKOI 1 , Hiroshi NAKAYAMA 1 , Yoichi ISHIDA 2 , Seiji NEMOTO 3 1Department of Neuropsychiatry, Gunma University School of Medicine 2Department of Pathology, Gunma University School of Medicine 3Kasamatsu Hospital pp.498-506
Published Date 1976/6/10
DOI https://doi.org/10.11477/mf.1431903855
  • Abstract
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1. Unusual familial cases of Binswanger's chronic progressive subcortical encephalopathy were described. The disease started in the third decade with steady progressive course leading to death in 8 or 9 years. The clinical picture was summarized as a combination of organic dementia, extrapyramidal disorders associated with pseudobulbar symptoms and marked pyramidal tract signs. The blood pressure remained always normal during the course.


Copyright © 1976, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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