(Q57998420)

English

Deep venous thrombosis in a patient with Behçet’s disease and homozygous prothrombin (factor II) G20210A mutation on oral contraceptive pills

scholarly article by Imad Uthman et al published 28 September 2005 in Rheumatology International

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Statements

scholarly article

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Deep venous thrombosis in a patient with Behçet’s disease and homozygous prothrombin (factor II) G20210A mutation on oral contraceptive pills (English)

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Behçet's disease

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deep vein thrombosis

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based on heuristic

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object named as

Ali Taher

3

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author name string

Imad Uthman

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Zaher Otrock

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publication date

28 September 2005

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Rheumatology International

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26

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8

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758-759

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https://scigraph.springernature.com/pub.10.1007/s00296-005-0048-5

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High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives

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https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Behçet's disease and thrombophilia

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https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High prevalence of Factor V Leiden mutation among healthy individuals and patients with deep venous thrombosis in Lebanon: is the eastern Mediterranean region the area of origin of this mutation?

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https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prothrombin 20210 G to A variation and thrombosis

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https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thrombosis associated with the prothrombin G-->A20210 mutation in Behçet's disease

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https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vascular involvement in Behçet's disease: relation with thrombophilic factors, coagulation activation, and thrombomodulin

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https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Letter from Lebanon

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https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A patient homozygous for a mutation in the prothrombin gene 3'-untranslated region associated with massive thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of factor V Leiden and prothrombin gene mutation with Behçet's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behçet's disease and deep vein thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vascular involvement in Behçet's disease: arterial and venous and vessels of all sizes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Procoagulant mutations and venous thrombosis in Behçet's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High prevalence of prothrombin G20210A mutation among patients with deep venous thrombosis in Lebanon

1 reference

https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prothrombin gene 20210 G-A mutation in the Turkish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intracardiac thrombosis in a case of Behcet's disease associated with the prothrombin 20210G-A mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16189654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00296-005-0048-5

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