Familial amyotrophic lateral sclerosis with onset in bulbar sign, benign clinical course, and Bunina bodies: a clinical, genetic, and pathological study of a Japanese family.
第一作者:
K,Tsuchiya
第一单位:
Department of Laboratory Medicine and Pathology, Tokyo Metropolitan Matsuzawa Hospital, Japan.
作者:
医学主题词
老年人(Aged);肌萎缩侧索硬化(Amyotrophic Lateral Sclerosis);脑(Brain);延髓麻痹, 进行性(Bulbar Palsy, Progressive);DNA突变分析(DNA Mutational Analysis);女(雌)性(Female);人类(Humans);包涵体(Inclusion Bodies);男(雄)性(Male);中年人(Middle Aged);运动神经元(Motor Neurons);突变, 误义(Mutation, Missense);神经变性(Nerve Degeneration);系谱(Pedigree);脊髓(Spinal Cord);超氧化物歧化酶(Superoxide Dismutase)
DOI
10.1007/s004010000237
PMID
11078211
发布时间
2019-08-12
- 浏览27
Acta neuropathologica
603-7页
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