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Volumn 65, Issue 1, 2005, Pages 141-143

Early-onset ALS with long-term survival associated with spastin gene mutation

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; SPASTIN;

EID: 22044432063     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000167130.31618.0a     Document Type: Article
Times cited : (44)

References (10)
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    • Ben Hamida, M.1    Hentati, F.2    Ben Hamida, C.3
  • 2
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    • A case of amyotrophic lateral sclerosis with a very slow progression over 44 years
    • Grohme K, Maravic MV, Gasser T, Borasio GD. A case of amyotrophic lateral sclerosis with a very slow progression over 44 years. Neuromuscul Disord 2001;11:414-416.
    • (2001) Neuromuscul Disord , vol.11 , pp. 414-416
    • Grohme, K.1    Maravic, M.V.2    Gasser, T.3    Borasio, G.D.4
  • 3
    • 2442658908 scopus 로고    scopus 로고
    • DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)
    • Chen YZ, Bennett CL, Huynh HM, et al. DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). Am J Hum Genet 2004;74:1128-1135.
    • (2004) Am J Hum Genet , vol.74 , pp. 1128-1135
    • Chen, Y.Z.1    Bennett, C.L.2    Huynh, H.M.3
  • 4
    • 0034785509 scopus 로고    scopus 로고
    • The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
    • Yang Y, Hentati A, Deng HX, et al. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nat Genet 2001;29:160-165.
    • (2001) Nat Genet , vol.29 , pp. 160-165
    • Yang, Y.1    Hentati, A.2    Deng, H.X.3
  • 5
    • 0032721512 scopus 로고    scopus 로고
    • Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
    • Kazan J, Fonknechten N, Mavel D, et al. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat Genet 1999;23:296-303.
    • (1999) Nat Genet , vol.23 , pp. 296-303
    • Kazan, J.1    Fonknechten, N.2    Mavel, D.3
  • 6
    • 0041522770 scopus 로고    scopus 로고
    • The hereditary spastic paraplegias: Nine genes and counting
    • Fink JK. The hereditary spastic paraplegias: nine genes and counting. Arch Neurol 2003;60:1045-1049.
    • (2003) Arch Neurol , vol.60 , pp. 1045-1049
    • Fink, J.K.1
  • 7
    • 0036483811 scopus 로고    scopus 로고
    • Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia
    • Meijer IA, Hand CK, Cossette P, et al. Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia. Arch Neurol 2002;59:281-6.
    • (2002) Arch Neurol , vol.59 , pp. 281-286
    • Meijer, I.A.1    Hand, C.K.2    Cossette, P.3
  • 8
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    • Hereditary spastic paraplegia: Spastin phenotype and function
    • Fink JK, Rainier S. Hereditary spastic paraplegia: spastin phenotype and function. Arch Neurol 2004;61:830-833.
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    • Fink, J.K.1    Rainier, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.