Myotonic Dystrophy-1 Complicated by Factor-V (Leiden) Mutation [PDF]
Case Reports in Medicine, 2015 Objectives. Presence of a factor-V Leiden mutation in a patient with myotonic dystrophy type 1 (DM1) has been reported only once. Here we report the second DM1 patient carrying a factor-V mutation who died from long-term complications of this mutation ...
Josef Finsterer, Claudia Stöllberger
doaj +5 more sources
Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis: results of a case-control study [PDF]
Blood, 2000 In a collaborative multicenter case-control study, we investigated the effect of factor V Leiden mutation, prothrombin gene mutation, and inherited deficiencies of protein C, protein S, and antithrombin on the risk of Budd-Chiari ...
Adang, R.P.R. (Rob) +11 more
core +3 more sources
Prevalence of the Factor V Leiden Mutation Arg534Gln in Western Region of Saudi Arabia: Functional Alteration and Association Study With Different Populations [PDF]
Clinical and Applied Thrombosis/Hemostasis, 2021 The rare Gln534 (Factor V Leiden; FVL) allele (1:169,519,049 T>C) is associated with an increased risk of venous thrombosis. The purpose of this study was to measure the prevalence of Factor V Leiden mutation in thrombophilia patients with deep vein ...
Mohammad Athar PhD +10 more
doaj +2 more sources
Factor V Leiden Mutation and Stroke
Pediatric 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 +3 more sources
Prevention of thromboembolic events after radical prostatectomy in patients with hereditary thrombophilia due to a factor V Leiden mutation by multidisciplinary coagulation management [PDF]
Asian Journal of UrologyObjective: To examine the perioperative impact of factor V Leiden mutation on thromboembolic events' risk in radical prostatectomy (RP) patients. With an incidence of about 5%, factor V Leiden mutation is the most common hereditary hypercoagulability ...
Randi M. Pose +8 more
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Impedimetric Sensing of Factor V Leiden Mutation by Zip Nucleic Acid Probe and Electrochemical Array [PDF]
Biosensors, 2020 A carbon nanofiber enriched 8-channel screen-printed electrochemical array was used for the impedimetric detection of SNP related to Factor V Leiden (FV Leiden) mutation, which is the most common inherited form of thrombophilia.
Arzum Erdem, Ece Eksin
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Prevalence of factor V Leiden mutation in various populations
Genetic Epidemiology, 1997 Resistance to activated protein C (APC) is the most common inherited risk factor for venous thrombosis. Most cases of APC resistance are caused by the point mutation nt 1691 G-A in factor V gene, referred to as factor V Leiden mutation. As initially shown in a Dutch population, this mutation has a carrier rate of 2.9%, the most frequent genetic ...
Falko H. Herrmann +7 more
semanticscholar +3 more sources
Factor V Leiden Mutation and Neonatal Stroke
Pediatric 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 +3 more sources
Isolated thrombosis of right spermatic vein with underlying Factor V Leiden mutation. [PDF]
Can Urol Assoc J, 2016 Bolat D +5 more
europepmc +2 more sources
The frequency of factor V G1691A (Leiden) mutation in the healthy Kazakh population [PDF]
Turkish Journal of Hematology, 2011 Hakkı Taştan
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