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

Acta Neuropathologica

Volumn 100, Issue 6, 2000, Pages 603-607

  Tsuchiya, K ^a   Shintani, S ^c   Nakabayashi, H ^d   Kikugawa, K ^e   Nakano, R ^e   Haga, C ^b   Nakano, I ^f   Ikeda, K ^b   Tsuji, S ^e  

^a TOKYO METROPOLITAN MATSUZAWA HOSPITAL   (Japan)

^b TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

^c Toride Kyodo General Hospital   (Japan)

^d JIKEI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^e NIIGATA UNIVERSITY   (Japan)

^f JICHI MEDICAL UNIVERSITY   (Japan)

Author keywords

Bunina bodies; Cu Zn superoxide dismutase; Familial amyotrophic lateral sclerosis; Neuropathology

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; UBIQUITIN;

ADULT; AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL INCLUSION; CELL LOSS; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DYSARTHRIA; DYSPHAGIA; FAMILIAL DISEASE; FAMILY HISTORY; FAMILY STUDY; FEMALE; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC SCREENING; HUMAN; JAPAN; LEWY BODY; MALE; MOTOR NEURON DISEASE; MUSCLE DISEASE; MUSCLE WEAKNESS; NERVE CELL; NEUROPATHOLOGY; ONSET AGE; PARALYSIS; PRIORITY JOURNAL; RESPIRATORY DISTRESS; SPINOCEREBELLAR TRACT; SURVIVAL;

AGED; AMYOTROPHIC LATERAL SCLEROSIS; BRAIN; BULBAR PALSY, PROGRESSIVE; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; INCLUSION BODIES; MALE; MIDDLE AGED; MOTOR NEURONS; MUTATION, MISSENSE; NERVE DEGENERATION; PEDIGREE; SPINAL CORD; SUPEROXIDE DISMUTASE;

EID: 0033770042     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004010000237     Document Type: Article

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