Results 31 to 40 of about 41,383 (293)

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

مجلة 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, Ferial Hilmi, Jaladet M.S. Jubrael, Ali M. Al-Ameri   +3 more
doaj   +1 more source

Do factor V Leiden and prothrombin G20210A mutations predict recurrent venous thromboembolism in older patients? [PDF]

, 2017
BACKGROUND The value of genetic thrombophilia testing in elderly patients with an unprovoked venous thromboembolism is unclear. We assessed whether the factor V Leiden and the prothrombin G20210A mutation are associated with recurrent venous ...
Limacher, Andreas, Beer, Hans-Jürg, Laemmle, Bernhard, Lämmle, B., Angelillo-Scherrer, A., Limacher, A., Beer, H.J., Aujesky, Drahomir, Drahomir Aujesky, Marie Méan, Alberio, Lorenzo, Alberio, L., Lämmle, Bernhard, Angelillo-Scherrer, Anne, Lorenzo Alberio, Aujesky, D., Rodondi, Nicolas, Andreas Limacher, Bernhard Lämmle, Anne Angelillo-Scherrer, Stalder, O., Hans-Jürg Beer, Pierre Fontana, Stalder, Odile, Angelillo, Anne, Odile Stalder, Méan, M., Méan, Marie, Nicolas Rodondi, Fontana, P., Rodondi, N., Fontana, Pierre   +31 more
core   +1 more source

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

Haematologica, 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, Adriana Ordóñez, Francisco España, José Ramón González-Porras, Ramón Lecumberri, Jordi Fontcuberta, Pilar Llamas, Francisco Marín, Amparo Estellés, Ignacio Alberca, Vicente Vicente, Javier Corral   +11 more
doaj   +1 more source

Prothrombin G20210A and Factor V Leiden mutations in ischemic arterial stroke

Van 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

Current evidence for outcomes of free-flap reconstruction in factor V Leiden patients

Australasian Journal of Plastic Surgery, 2019
**Background**: Factor V Leiden is the most common form of inherited thrombophilic syndrome, affecting 5 per cent of Caucasians. While increased rates of venous thromboembolic complications have been regularly reported in factor V Leiden patients, little
Isobel Yeap, Chris Ahn, Stuart Hoffman, Rowan Gillies, John Vandervord   +4 more
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

Journal 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, Niclas Eriksson, Stephanie Ross, Daniel M. F. Claassens, Folkert W. Asselbergs, Karina Meijer, Agneta Siegbahn, Stefan James, Guillaume Pare, Lars Wallentin, Jurriën M. ten Berg   +10 more
doaj   +1 more source

The frequency of factor V Leiden and concomitance of factor V Leiden

, 2007
Factor V Leiden causing activated protein C resistance is the most common inherited form of thrombophilia leading to thrombosis. Its frequency shows great ethnic and geographic variations. The aim of this study was to determine the frequency of FV Leiden and coinheritance of FV Leiden with two other frequent hereditary thrombophilia causes, namely ...
Kabukcu, S, Keskin, N, Keskin, A, Atalay, E   +3 more
openaire   +2 more sources

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

Iranian 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, Samieh Karimi, Majid Yavarian, Minoo Rajaei, Maryam Azizi Kootenaee   +4 more
doaj  

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

Journal 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, Kakoli Acharyya, Archana Parasar, Shanto Pramanik   +3 more
doaj   +1 more source

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

Diagnostics, 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