Associated Papers
Effect of gene-gene and gene-environment interaction on the risk of first-ever stroke and poststroke death.
Feng C et al.
Molecular Genetics & Genomic Medicine, 2019
31293107 (PubMed )
Supplement: MGG3-7-e846-s001.docx
Central retinal artery occlusion in a 13-year-old child as a presenting sign of hyperhomocysteinemia together with high lipoprotein(a) level.
Coban-Karatas M et al.
Pediatric Neurology, 2013
Interaction of genetic risk factors confers higher risk for thrombotic stroke in male Chinese: a multicenter case-control study.
Shen CD et al.
Annals of Human Genetics, 2007
Moya moya syndrome in a child with pyruvate kinase deficiency and combined prothrombotic factors.
Skardoutsou A et al.
Journal of Child Neurology, 2007
Homocysteine and carotid intima-media thickness in a german population: lack of clinical relevance.
Linnebank M et al.
Stroke, 2006
Homozygosity for factor V Leiden mutation and ischemic stroke: two case-reports and review of the literature.
Allroggen A et al.
Journal of Neurology, 2004
The factor V G1691A mutation is a risk for porencephaly: A case-control study.
Debus OM et al.
Annals of Neurology, 2004
The 677C-->T mutation of the methylene-tetrahydrofolate reductase gene in the pathogenesis of osteonecrosis of the femoral head.
Zalavras CG et al.
Haematologica, 2002
Relation of a common methylenetetrahydrofolate reductase mutation and plasma homocysteine with intimal hyperplasia after coronary stenting.
Kosokabe T et al.
Circulation, 2001
Polymorphism in methylenetetrahydrofolate reductase gene: its impact on plasma homocysteine levels and carotid atherosclerosis in ESRD patients receiving hemodialysis.
Lim PS et al.
Nephron, 2001
A methylenetetrahydrofolate reductase gene polymorphism in ischaemic stroke and in carotid artery stenosis.
Kostulas K et al.
European Journal of Clinical Investigation, 1998
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