(Q43725131)

26 November 2017

title

Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden (English)

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26 November 2017

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1

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26 November 2017

2

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26 November 2017

Ronald L Nagel

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26 November 2017

Adriana Muniz

series ordinal

4

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26 November 2017

language of work or name

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11 July 2007

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Journal of Thrombosis and Thrombolysis

26 November 2017

published in

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26 November 2017

volume

25

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26 November 2017

issue

3

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26 November 2017

page(s)

288-292

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https://scigraph.springernature.com/pub.10.1007/s11239-007-0069-x

26 November 2017

exact match

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cites work

Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease

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12 December 2020

Hypercoagulability in sickle cell disease: a curious paradox

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12 December 2020

Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil

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12 December 2020

Thrombophilic mutations in Iran

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12 December 2020

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

12 December 2020

Should we screen Eastern Mediterranean sickle beta-thalassemia patients for inherited thrombophilia?

1 reference

12 December 2020

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

1 reference

12 December 2020

Reverse dot blot probes for the screening of beta-thalassemia mutations in Asians and American blacks

1 reference

12 December 2020

Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia

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12 December 2020

Screening for inherited thrombophilia might be warranted among Eastern Mediterranean sickle-ßeta-0 thalassemia patients

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12 December 2020

Recurrent thromboembolism in a patient with beta-thalassemia major associated with double heterozygosity for factor V R506Q and prothrombin G20210A mutations

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12 December 2020

Plasma lipids in Iranians with sickle cell disease: hypocholesterolemia in sickle cell anemia and increase of HDL-cholesterol in sickle cell trait

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12 December 2020

Varied prevalence of factor V G1691A (Leiden) and prothrombin G20210A single nucleotide polymorphisms among Arabs

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12 December 2020

10.1007/S11239-007-0069-X

Identifiers

DOI

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26 November 2017

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