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Neurology
Volumn 70, Issue 13, 2008, Pages 1054-1055
Melas associated with mutations in the polg1 gene
Author keywords

[No Author keywords available]
Indexed keywords

ELECTROENCEPHALOGRAM; EPILEPSY; GENE; GENE MUTATION; HEADACHE; HUMAN; LETTER; MELAS SYNDROME; MIGRAINE; NUCLEAR MAGNETIC RESONANCE IMAGING; POLG 1 GENE; PRIORITY JOURNAL; STROKE;
EID: 41349100269     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/01.wnl.0000307661.98694.c3     Document Type: Letter
Times cited : (10)
References (8)
  • 1
    • 34248586627 scopus 로고    scopus 로고
    • MELAS associated with mutations in the POLG1 gene.
    • Deschauer M, Tennant S, Rokicka A, et al. MELAS associated with mutations in the POLG1 gene. Neurology 2007;68:1741-1742.
    • (2007) Neurology , vol.68 , pp. 1741-1742
    • Deschauer, M.1    Tennant, S.2    Rokicka, A.3
  • 2
    • 16844382687 scopus 로고    scopus 로고
    • Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations.
    • Winterthun S, Ferrari G, He L, et al. Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations. Neurology 2005;64:1204-1208.
    • (2005) Neurology , vol.64 , pp. 1204-1208
    • Winterthun, S.1    Ferrari, G.2    He, L.3
  • 3
    • 33745685519 scopus 로고    scopus 로고
    • The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases.
    • Tzoulis C, Engelsen BA, Telstad W, et al. The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases. Brain 2006;129:1685-1692.
    • (2006) Brain , vol.129 , pp. 1685-1692
    • Tzoulis, C.1    Engelsen, B.A.2    Telstad, W.3
  • 4
    • 0242494492 scopus 로고    scopus 로고
    • Slowly progressive spread of the stroke-like lesions in MELAS.
    • Iizuka T, Sakai F, Kan S, Suzuki N. Slowly progressive spread of the stroke-like lesions in MELAS. Neurology 2003;61:1238-1244.
    • (2003) Neurology , vol.61 , pp. 1238-1244
    • Iizuka, T.1    Sakai, F.2    Kan, S.3    Suzuki, N.4
  • 5
    • 0032707838 scopus 로고    scopus 로고
    • The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS.
    • Pulkes T, Eunson L, Patterson V, et al. The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS. Ann Neurol 1999;46:916-919.
    • (1999) Ann Neurol , vol.46 , pp. 916-919
    • Pulkes, T.1    Eunson, L.2    Patterson, V.3
  • 6
    • 4744344532 scopus 로고    scopus 로고
    • Mutations of the mitochondrial ND1 gene as a cause of MELAS.
    • Kirby DM, McFarland R, Ohtake A, et al. Mutations of the mitochondrial ND1 gene as a cause of MELAS. J Med Genet 2004;41:784-789.
    • (2004) J Med Genet , vol.41 , pp. 784-789
    • Kirby, D.M.1    McFarland, R.2    Ohtake, A.3
  • 7
    • 0021143782 scopus 로고
    • Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.
    • Pavlakis SG, Phillips PC, DiMauro S, De Vivo DC, Rowland LP. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome. Ann Neurol 1984;16:481-488.
    • (1984) Ann Neurol , vol.16 , pp. 481-488
    • Pavlakis, S.G.1    Phillips, P.C.2    DiMauro, S.3    De Vivo, D.C.4    Rowland, L.P.5
  • 8
    • 33745713884 scopus 로고    scopus 로고
    • Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.
    • Horvath R, Hudson G, Ferrari G, et al. Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Brain 2006;129:1674-1684.
    • (2006) Brain , vol.129 , pp. 1674-1684
    • Horvath, R.1    Hudson, G.2    Ferrari, G.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.