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Article

G20210A prothrombin gene mutation in two siblings with cerebral venous thrombosis.

Neurology - 1 Jul 1998

Huberfeld G, Kubis N, Lot G, Ripoll L, Chaine P, Drouet L, Woimant F

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PMID: 9674835
DOI: 10.1212/wnl.51.1.316

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

G20210A prothrombin gene mutation in two siblings with cerebral venous thrombosis.PMID 9674835Read ↗

Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.Semantic proximity Read ↗

Double-homozygosity for factor V Leiden and the prothrombin gene G20210A variant in a young patient with idiopathic venous thrombosis.Semantic proximity Read ↗

Prothrombin gene variant (G20210A) in a patient with cerebral venous sinus thrombosis.Semantic proximity Read ↗

Superior sagittal sinus thrombosis in a patient heterozygous for the novel 20210 A allele of the prothrombin gene.Semantic proximity Read ↗

Cerebral venous sinus thrombosis in a neonate with homozygous prothrombin G20210A genotype.Semantic proximity Read ↗

Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.Semantic proximity Read ↗

Idiopathic central retinal vein occlusion in 2 siblings with the 20210 G-->A prothrombin variant.Semantic proximity Read ↗

Venous thromboembolism in a young woman with combined homozygosity for factor V Leiden and prothrombin G20210A mutations.Semantic proximity Read ↗

A further case of homozygous G20210A prothrombin gene mutation without thromboembolic events.Semantic proximity Read ↗

Antithrombin Cambridge II mutation as a risk factor to develop cerebral venous thrombosis.Semantic proximity Read ↗

Cerebral venous sinus thrombosis in child with antithrombin deficiency and novel SERPINC1 variant.Semantic proximity Read ↗

Homozygous 20210G/A prothrombin gene mutation associated with bilateral iliac vein thrombosis: a case report.Semantic proximity Read ↗

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