A common polymorphism in the methylenetetrahydrofolate reductase gene, homocysteine, and ischemic cerebrovascular disease.
about
The Siblings With Ischemic Stroke Study (SWISS) protocolHaplotype analysis of the CYP8A1 gene associated with myocardial infarctionThermolabile MTHFR genotype and retinal vascular occlusive diseaseGenetics of atherothrombotic and lacunar strokeNutrigenomics in cardiovascular medicine.Stroke in childhood.Total homocysteine and cardiovascular disease.Thrombophilia, polymorphisms, and vascular diseaseRisk factors for arterial ischemic stroke in children.Etiology and pathophysiology of stroke as a complex trait.Novel risk factors for stroke: homocysteine, inflammation, and infection.Homocysteine, vitamins, and coronary artery disease. Comprehensive review of the literaturePolymorphisms in the methylenetetrahydrofolate reductase gene: clinical consequences.Homocyst(e)ine and cardiovascular disease: a systematic review of the evidence with special emphasis on case-control studies and nested case-control studies.Genetic aspects of stroke: human and experimental studies.Quantitative assessment of association between rs1801133 polymorphism and susceptibility to stroke.Risk factors for ischaemic stroke.Stroke pharmacogenomics.Predictive value of homocysteine for depression after acute coronary syndromeGenetic aspects of ischemic stroke: coagulation, homocysteine, and lipoprotein metabolism as potential risk factors.Advances in understanding stroke risk in children--a geneticist's view.Homocysteine excess: delineating the possible mechanism of neurotoxicity and depression.Utilizing nutritional genomics to tailor diets for the prevention of cardiovascular disease: a guide for upcoming studies and implementations.Higher incidence of C677T polymorphism of the MTHFR gene in North Indian patients with vascular disease.Red cell N5-methyltetrahydrofolate concentrations and C677T methylenetetrahydrofolate reductase genotype in patients with stroke.Homocysteine in neuropsychiatric disorders of the elderly.Prevalence of thrombophilic mutations and ACE I/D polymorphism in Turkish ischemic stroke patients.[Atherosclerosis and uremia: signifance of non-traditional risk factors].[Homocysteine and neuropsychiatric disorders].Genotype and allele frequencies of the polymorphic methylenetetrahydrofolate reductase gene in Turkey.Methylenetetrahydrofolate reductase gene A222V polymorphism and risk of ischemic stroke.MTHFR C677T gene mutation as a risk factor for arterial stroke: a hospital based study.Stroke in children: inherited and acquired factors and age-related variations in the presentation of 48 paediatric patients.C677T polymorphism of the methylenetetrahydrofolate reductase gene and the risk of ischemic stroke in Polish subjects.Severe central nervous system thrombotic events in hemoglobin Sabine patient.Methylenetetrahydrofolate reductase polymorphism, plasma homocysteine and age.Absence of association between a common mutation in the methylenetetrahydrofolate reductase gene and preeclampsia in Japanese women.Methylene tetrahydrofolate reductase mutation and stroke in a monozygotic twinHomozygous thermolabile variant of the methylenetetrahy-drofolate reductase gene: a potential risk factor for hyperhomo-cysteinaemia, CVD, and stroke in childhoodFatal haemorrhagic infarct in an infant with homocystinuria
P2860
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P2860
A common polymorphism in the methylenetetrahydrofolate reductase gene, homocysteine, and ischemic cerebrovascular disease.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
A common polymorphism in the m ...... hemic cerebrovascular disease.
@en
A common polymorphism in the m ...... hemic cerebrovascular disease.
@nl
type
label
A common polymorphism in the m ...... hemic cerebrovascular disease.
@en
A common polymorphism in the m ...... hemic cerebrovascular disease.
@nl
prefLabel
A common polymorphism in the m ...... hemic cerebrovascular disease.
@en
A common polymorphism in the m ...... hemic cerebrovascular disease.
@nl
P2093
P356
P1433
P1476
A common polymorphism in the m ...... hemic cerebrovascular disease.
@en
P2093
A Sankaralingam
H S Markus
R Swaminathan
P304
P356
10.1161/01.STR.28.9.1739
P407
P577
1997-09-01T00:00:00Z