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Volumn 65, Issue 4, 2008, Pages 537-539

Geriatric neurogenetics: Oxymoron or reality?

Author keywords

[No Author keywords available]

Indexed keywords

AGED; AGING; ALZHEIMER DISEASE; ANAMNESIS; AUTOSOMAL DOMINANT INHERITANCE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; ELECTROMYOGRAM; FEMALE; GENE MUTATION; GENETIC DISORDER; GENETIC SCREENING; GERIATRIC CARE; HUMAN; HUNTINGTON CHOREA; LIMB GIRDLE MUSCULAR DYSTROPHY; MALE; NEUROLOGIC DISEASE; OUTCOME ASSESSMENT; PERIPHERAL NEUROPATHY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; REVIEW; SPINOCEREBELLAR DEGENERATION;

EID: 42249090571     PISSN: 00039942     EISSN: 15383687     Source Type: Journal    
DOI: 10.1001/archneur.65.4.537     Document Type: Review
Times cited : (12)

References (7)
  • 1
    • 20144388593 scopus 로고    scopus 로고
    • The clinical and genetic spectrum of spinocerebellar ataxia 14
    • Chen DH, Cimino PJ, Ranum LP, et al. The clinical and genetic spectrum of spinocerebellar ataxia 14. Neurology. 2005;64(7):1258-1260.
    • (2005) Neurology , vol.64 , Issue.7 , pp. 1258-1260
    • Chen, D.H.1    Cimino, P.J.2    Ranum, L.P.3
  • 2
    • 31744441984 scopus 로고    scopus 로고
    • Spectrin mutations cause spinocerebellar ataxia type 5
    • Ikeda Y, Dick KA, Weatherspoon MR, et al. Spectrin mutations cause spinocerebellar ataxia type 5. Nat Genet. 2006;38(2):184-190.
    • (2006) Nat Genet , vol.38 , Issue.2 , pp. 184-190
    • Ikeda, Y.1    Dick, K.A.2    Weatherspoon, M.R.3
  • 3
    • 34848839240 scopus 로고    scopus 로고
    • Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease
    • Brickell KL, Leverenz JB, Steinbart EJ, et al. Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease. J Neurol Neurosurg Psychiatry. 2007;78(10):1050- 1055.
    • (2007) J Neurol Neurosurg Psychiatry , vol.78 , Issue.10 , pp. 1050-1055
    • Brickell, K.L.1    Leverenz, J.B.2    Steinbart, E.J.3
  • 6
    • 33748684424 scopus 로고    scopus 로고
    • Late-onset metachromatic leukodystrophy: Genotype strongly influences phenotype
    • Rauschka H, Colsch B, Baumann N, et al. Late-onset metachromatic leukodystrophy: genotype strongly influences phenotype. Neurology. 2006;67(5):859-863.
    • (2006) Neurology , vol.67 , Issue.5 , pp. 859-863
    • Rauschka, H.1    Colsch, B.2    Baumann, N.3
  • 7
    • 28944450552 scopus 로고    scopus 로고
    • Late-onset Friedreich ataxia: Phenotypic analysis, magnetic resonance imaging findings, and review of the literature
    • Bhidayasiri R, Perlman SL, Pulst S-M, Geschwind DH. Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature. Arch Neurol. 2005;62(12):1865-1869.
    • (2005) Arch Neurol , vol.62 , Issue.12 , pp. 1865-1869
    • Bhidayasiri, R.1    Perlman, S.L.2    Pulst, S.-M.3    Geschwind, D.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.