Brain stem gliosis in a case with clinical manifestations of amyotrophic lateral sclerosis.

作者: Naohiko Takahata , Toshio Yamanouchi , Ryo Fukatsu , Mizuho Katagiri

DOI: 10.1111/J.1440-1819.1976.TB00109.X

关键词:

摘要: Summary A 32-year-old male with typical clinical course of progressive bulbar paresis was investigated histopathologically. The main pathological change prominent fibrous gliosis in the brain stem and cervical cord without remarkable nerve cell loss same area. Concerning pathogenesis this case, significance primary role discussed.

参考文章(9)
INGRID V. ALLEN, EVELYN DERMOTT, J. H. CONNOLLY, L. J. HURWITZ, A STUDY OF A PATIENT WITH THE AMYOTROPHIC FORM OF CREUTZFELDT-JAKOB DISEASE Brain. ,vol. 94, pp. 715- 724 ,(1971) , 10.1093/BRAIN/94.4.715
K. von Matt, Progressive Bulbärparalyse und dementielles Syndrom European Neurology. ,vol. 148, pp. 354- 364 ,(1964) , 10.1159/000128869
A.F. Thomson, F.A. Alvarez, Hereditary amyotrophic lateral sclerosis Journal of the Neurological Sciences. ,vol. 8, pp. 101- 110 ,(1969) , 10.1016/0022-510X(69)90044-6