Results 11 to 20 of about 41,383 (293)

SV-IV Peptide1–16 reduces coagulant power in normal Factor V and Factor V Leiden [PDF]

open access: yesJournal of Translational Medicine, 2007
Native Factor V is an anticoagulant, but when activated by thrombin, Factor X or platelet proteases, it becomes a procoagulant. Due to these double properties, Factor V plays a crucial role in the regulation of coagulation/anticoagulation balance. Factor
Ferrazzi Paola   +6 more
doaj   +2 more sources

Factor V Leiden Mutation in Iraqi Patients with Deep Venous Thrombosis.

open access: yesمجلة كلية الطب, 2011
Background: Factor V Leiden is considered the most common inherited risk factor for venous thrombosis in Caucasian populations, including those in the Eastern Mediterranean region.
Nasir Al-Allawi   +2 more
doaj   +3 more sources

Factor V Leiden Mutation and Stroke

open access: yesPediatric Neurology Briefs, 2001
The association of the factor V Leiden mutation and cerebrovascular disorder (CVD) in children is reviewed and the clinical features of 8 children with cerebral palsy (CP) and the Leiden mutation are described from the National Institute of Neurological ...
J Gordon Millichap
doaj   +2 more sources

Factor V Leiden and Cardiopulmonary Bypass

open access: yesThe Journal of ExtraCorporeal Technology, 2015
We present a case of a patient with factor V Leiden with an antithrombin III activity of 67% who received a successful aortic valve replacement supported by cardiopulmonary bypass (CPB). A safe level of anticoagulation was achieved by monitoring activated clotting time (ACT) and heparin concentration ensuring adequate anticoagulation throughout the ...
Victor, Uppal   +5 more
openaire   +3 more sources

Factor V Leiden Mutation in Cerebrovascular Disease

open access: yesClinical and Applied Thrombosis/Hemostasis, 2005
Several studies indicate a high prevalence of factor V Leiden mutation as the most frequent coagulation defect found in patients with venous thrombosis. The relationship between this mutation and cerebrovascular disease has not been established in adults.
Buyru, N   +3 more
openaire   +3 more sources

Factor V Leiden Mutation and Neonatal Stroke

open access: yesPediatric Neurology Briefs, 1997
Three infants with familial factor V Leiden mutation and neonatal cerebrovascular disorders are reported from the Children’s Hospital of Philadelphia, PA.
J Gordon Millichap
doaj   +2 more sources

Factor V Leiden Mutation and its Impact on Pregnancy Complications

open access: yesActa Medica, 2011
Objective: The aim of this prospective study was to find the association between the factor V Leiden mutation and adverse pregnancy outcomes. Methods: This study is an analysis of a prospective observational study of the frequency of placenta-mediated ...
Ľubica Hammerová   +3 more
doaj   +2 more sources

Factor V G1691A (Leiden) is a major etiological factor in Egyptian Budd-Chiari syndrome patients

open access: yesTurkish Journal of Hematology, 2011
OBJECTIVE: Budd-Chiari syndrome is a multifactorial disease in which several prothrombotic disorders may predispose patients to the development of thrombosis at this uncommon location (hepatic veins). The aim of this study was to determine the prevalence
Tawhida Y. Abdel Ghaffar   +7 more
doaj   +4 more sources

Regional block anesthesia in a patient with factor V Leiden mutation and axillary artery occlusion

open access: yesLocal and Regional Anesthesia, 2011
Kerem Erkalp1, Mevlut Comlekci1, Bekir Inan2, Gokcen Basaranoglu1, Haluk Ozdemir1, Leyla Saidoglu11Department of Anaesthesiology and Reanimation, Vakif Gureba Hospital, Istanbul, Turkey; 2Department of Vascular Surgery, Vakif Gureba Hospital, Istanbul ...
Kerem Erkalp   +3 more
doaj   +1 more source

Factor V Leiden and Prothrombin Mutations in South of Iran

open access: yesArmaghane Danesh Bimonthly Journal, 2007
: Introduction & Objective: Factor V Leiden and prothrombin mutation are not common but they are involved in pediatric thrombosis. The aim of this study was to evaluate the frequency of factor V Leiden & prohtrombin mutation in healthy population of ...
M Karimi, AR Panahande, AR Afrasiabi
doaj   +1 more source

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