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Volumn 37, Issue 4, 1995, Pages 452-459

A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four european families

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN ATROPHY; CEREBELLAR ATAXIA; CHOREA; CHROMOSOME 12; CONTROLLED STUDY; DEGENERATIVE DISEASE; DEMENTIA; DENTATE NUCLEUS; DYSTONIA; EPILEPSY; FEMALE; GENE MUTATION; GLOBUS PALLIDUS; HUMAN; HUNTINGTON CHOREA; MAJOR CLINICAL STUDY; MALE; MYOCLONUS; PARKINSONISM; PEDIGREE; PRIORITY JOURNAL; PSYCHOSIS; RED NUCLEUS;

EID: 0028958153     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.410370407     Document Type: Article
Times cited : (69)

References (19)
  • 2
    • 0020064620 scopus 로고
    • Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral‐pallidoluysian atrophy
    • (1982) Neurology , vol.32 , pp. 798-802
    • Naito, H.1    Oyanagi, S.2
  • 12
    • 0026536877 scopus 로고
    • “Haw River syndrome” or dentatorubropallidoluysian atrophy?
    • (1992) Arch Neurol , vol.49 , pp. 13-14
    • Singer, C.1
  • 15
    • 0025283203 scopus 로고
    • McComb RD. Dentatorubro‐pallidoluysian atrophy of the myoclonus epilepsy type with posterior column degeneration
    • (1990) Mov Disord , vol.5 , pp. 134-138
    • Pfeiffer, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.