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Article

C677T MTHFR Mutation and Factor V Leiden Mutation in Patients with TIA/Minor Stroke

1 Jan 1999

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Share to Blood Coagulation and Thrombosis Mechanisms
Share to Neurological Complications and Syndromes
Share to Venous Thromboembolism Diagnosis and Management

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9950259
DOI: 10.1016/s0049-3848(98)00154-6

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C677T MTHFR Mutation and Factor V Leiden Mutation in Patients with TIA/Minor StrokePMID 9950259Read ↗

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Association between C807T(C/T) polymorphism of platelet glycoprotein gene and sensitivity to ischemic stroke: a meta-analysis.Semantic proximity Read ↗

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Factor V Leiden and MTHFR mutations as a combined risk factor for hypercoagulability in referred Patients population from Western IndiaSemantic proximity Read ↗

No association between the MTHFR A1298C and transcobalamin C776G genetic polymorphisms and hyperhomocysteinemia in thrombotic disease.Semantic proximity Read ↗

Do common prothrombotic mutations influence the risk of cerebral ischaemia in patients with patent foramen ovale? Systematic review and meta-analysis.Semantic proximity Read ↗

Very rare minor homozygous GG genotype of tissue factor +5466A>G mutation in a patient with two cryptogenic cerebrovascular ischemic events.Semantic proximity Read ↗

MTHFR C677T polymorphism and its relation to ischemic stroke in the Black Sea Turkish population.Semantic proximity Read ↗

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