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Volumn 53, Issue 6, 1999, Pages 1332-1335

Moyamoya disease in Italian monozygotic twins

Author keywords

Genetics; Human leukocyte antigen; Methylenetetrahydrofolate reductase; Monozygotic twins; Moyamoya; Stroke

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);

EID: 0032880708     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.53.6.1332     Document Type: Article
Times cited : (18)

References (10)
  • 1
    • 0030715614 scopus 로고    scopus 로고
    • Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis ("moyamoya" disease). Research Committee on Spontaneous Occlusion of the Circle of Willis (moyamoya disease) of the Ministry of Health and Welfare
    • Fukui M. Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis ("moyamoya" disease). Research Committee on Spontaneous Occlusion of the Circle of Willis (moyamoya disease) of the Ministry of Health and Welfare, Japan. Clin Neurol Neurosurg 1997:99(suppl 2): S238-S240.
    • (1997) Japan. Clin Neurol Neurosurg , vol.99 , Issue.2 SUPPL.
    • Fukui, M.1
  • 3
    • 33747149870 scopus 로고    scopus 로고
    • DNA typing of HLA in the patients with moyamoya disease
    • Inoue TK, Ikezaki K, Sasazuki T, et al. DNA typing of HLA in the patients with moyamoya disease. Jpn J Hum Genet 1997; 42:507-515.
    • (1997) Jpn J Hum Genet , vol.42 , pp. 507-515
    • Inoue, T.K.1    Ikezaki, K.2    Sasazuki, T.3
  • 7
    • 0030728742 scopus 로고    scopus 로고
    • Association of methylenetetrahydrofolate reductase gene polymorphism with carotid arterial wall thickening and myocardial infarction risk in NIDDM
    • Arai K, Yamasaki Y, Kajimoto Y, et al. Association of methylenetetrahydrofolate reductase gene polymorphism with carotid arterial wall thickening and myocardial infarction risk in NIDDM. Diabetes 1997;46:2102-2104.
    • (1997) Diabetes , vol.46 , pp. 2102-2104
    • Arai, K.1    Yamasaki, Y.2    Kajimoto, Y.3
  • 8
    • 0029655724 scopus 로고    scopus 로고
    • Molecular genetic analysis in mild hyperhomocysteinemia: A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease
    • Kluijtmans LAJ, van den Heuvel LPWJ, Boers GHJ, et al. Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease. Am J Hum Genet 1996;58:35-41.
    • (1996) Am J Hum Genet , vol.58 , pp. 35-41
    • Kluijtmans, L.A.J.1    Van Den Heuvel, L.P.W.J.2    Boers, G.H.J.3
  • 9
    • 0031967236 scopus 로고    scopus 로고
    • Hyperhomocysteinemia and premature vascular occlusive disease
    • Guba SC, Fink LM, Fonseca V. Hyperhomocysteinemia and premature vascular occlusive disease. Am J Med Sci 1998;315: 279-285.
    • (1998) Am J Med Sci , vol.315 , pp. 279-285
    • Guba, S.C.1    Fink, L.M.2    Fonseca, V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.