Results 21 to 30 of about 38,180 (186)

Evaluation of Genetic and Environmental Risk Factors for Deep Vein Thrombosis in Sudanese [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2018
Introduction: Thrombophilia is a multi-factorial hypercoagulability disorder. The predisposing factors may be inherited, acquired or both. Factor V Leiden prothrombin 20210G>A mutations are the most common inherited factors.
Nadir Ahmed Ibrahim   +3 more
doaj   +1 more source

Freqüência do fator V Leiden em indivíduos sob investigação de trombofilia, Recife, Pernambuco, Brasil Frequency of factor V Leiden in individuals under thrombophilia investigation, Recife, Pernambuco, Brazil

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2006
As tromboses são eventos de etiopatogênese multifatorial resultantes da interação de fatores genéticos e ambientais, constituindo na atualidade uma das causas mais comuns de morbimortalidade.
Catarina P. S. Ramos   +6 more
doaj   +1 more source

Factor V Leiden and venous thrombosis: First case report from Iraq

open access: yesمجلة كلية الطب, 2005
Background: Factor V Leiden mutation is the most common cause of hereditary thrombophilia . this mutation was found to be highly prevalent in the Eastern Mediterranean region , with recently reported prevalence of 3% in random Iraqi blood donors.
Nasir AL-Allawi   +3 more
doaj   +1 more source

AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms

open access: yesHaematologica, 2008
Background Routine analyses for thrombophilia include determination of the presence of factor V Leiden and prothrombin 20210A polymorphisms. However, the usefulness of these determinations is controversial and the clinical benefit remains questioned ...
Antonia Miñano   +11 more
doaj   +1 more source

Prothrombin G20210A and Factor V Leiden mutations in ischemic arterial stroke

open access: yesVan Tıp Dergisi, 2018
INTRODUCTION: Ischemic stroke remains an important public health problem in all over world. It is wellknown that, some type of genetic mutations such as factor V Leiden and prothrombin G20210A contribute to the risk of ischemic venous stroke.
Hafize Nalan Güneş
doaj   +1 more source

Factor V Leiden and the Risk of Bleeding in Patients With Acute Coronary Syndromes Treated With Antiplatelet Therapy: Pooled Analysis of 3 Randomized Clinical Trials

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2021
Background Whether factor V Leiden is associated with lower bleeding risk in patients with acute coronary syndromes using (dual) antiplatelet therapy has yet to be investigated.
Bakhtawar K. Mahmoodi   +10 more
doaj   +1 more source

Prevalence and Clinical Significance of Factor V Leiden Mutation in Egyptian Preeclamptic Women [PDF]

open access: yesInternational Journal of Medical Arts, 2021
Background: Factor V [Leiden] mutation, also known as activated protein-C resistance, is the most common of the inherited thrombophilias. Aim of the work: The present study aimed to ass the prevalence of factor V Leiden mutation in a group of Egyptian ...
Ahmed Alsheikh   +2 more
doaj   +1 more source

Evaluation the frequency of factor V Leiden mutation in pregnant women with preeclampsia syndrome in an Iranian population [PDF]

open access: yesIranian Journal of Reproductive Medicine, 2012
Background: Role of genetic factors in etiology of preeclampsia is not confirmed yet.Objective: Gene defect frequency varies in different geographic areas as well as ethnic groups.
Azadeh Azinfar   +4 more
doaj  

Systematic Review and Meta-Analysis of the Susceptibility of ABO Blood Groups to Venous Thromboembolism in Individuals with Factor V Leiden

open access: yesDiagnostics, 2022
A limited number of studies investigated the association between the ABO blood groups and the incidence of venous thromboembolism in individuals with Factor V Leiden; however, discordant findings were reported.
Waleed M. Bawazir
doaj   +1 more source

Attenuation of phenotypical expression of severe hemophilia A in presence of simultaneous prothrombotic Factor V mutation: The debate continues

open access: yesJournal of Family Medicine and Primary Care, 2019
The effect of coexistence of the prothrombotic Factor V Leiden mutation on the phenotypical expression in hemophilia is still debatable. Six-year-old boy with severe hemophilia A had presented with large soft tissue hematoma, treated with Factor VIII ...
Saugata Acharyya   +3 more
doaj   +1 more source

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