(Q50534991)

14 March 2018

title

C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: a case-control study. (English)

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14 March 2018

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5

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14 March 2018

author name string

Lalouschek W

1

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14 March 2018

Aull S

2

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14 March 2018

Serles W

3

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14 March 2018

Schnider P

4

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14 March 2018

Pabinger-Fasching I

6

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14 March 2018

Deecke L

7

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14 March 2018

Zeiler K

8

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14 March 2018

publication date

1 January 1999

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14 March 2018

published in

Thrombosis Research

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14 March 2018

volume

93

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14 March 2018

issue

2

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14 March 2018

page(s)

61-69

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14 March 2018

Prospective study of serum total homocysteine concentration and risk of stroke in middle-aged British men.

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A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes

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7 January 2021

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

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7 January 2021

Genetic analysis of thermolabile methylenetetrahydrofolate reductase as a risk factor for myocardial infarction.

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7 January 2021

Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine metabolism and late-onset vascular disease.

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Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation

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7 January 2021

Distribution in healthy and coronary populations of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation

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7 January 2021

A common polymorphism in the methylenetetrahydrofolate reductase gene, homocysteine, and ischemic cerebrovascular disease.

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Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study

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Resistance to activated protein C as a basis for venous thrombosis.

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Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men

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Factor V gene mutation causing inherited resistance to activated protein C as a basis for venous thromboembolism

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7 January 2021

Ischemic stroke in the elderly. Role of the common factor V mutation causing resistance to activated protein C

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Activation of endogenous factor V by a homocysteine-induced vascular endothelial cell activator

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7 January 2021

Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosis

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7 January 2021

Interrelation of hyperhomocyst(e)inemia, factor V Leiden, and risk of future venous thromboembolism

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7 January 2021

A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506).

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Special report from the National Institute of Neurological Disorders and Stroke. Classification of cerebrovascular diseases III

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7 January 2021

Determination of free and total homocysteine in human plasma by high-performance liquid chromatography with fluorescence detection

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7 January 2021

Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease

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7 January 2021

The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia

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7 January 2021

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

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7 January 2021

Reduced response to activated protein C is associated with increased risk for cerebrovascular disease.

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7 January 2021

Myocardial infarction, Arg 506 to Gln factor V mutation, and activated protein C resistance.

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7 January 2021

World distribution of factor V Leiden

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2898%2900154-6

7 January 2021

10.1016/S0049-3848(98)00154-6

Identifiers

DOI

1 reference

14 March 2018

1 reference

14 March 2018