Si mostrano 100 riferimenti a partire da 1 |
Per ulteriori informazioni selezionare i riferimenti di interesse.
The impact of Factor V mutation on the risk for occlusion in patients undergoing peripheral vascular reconstructions
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY
ProC global: A new automated screening assay for the evaluation of total function of the protein C system
CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
Factor V Leiden and prothrombin G20210A in relation to arterial and/or vein rethrombosis: Two cases
CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
Coexistence of the methylenetetrahydrofolate reductase single-nucleotide polymorphism (C677T) in patients with the factor V Leiden or prothrombin G20210A polymorphisms
DIAGNOSTIC MOLECULAR PATHOLOGY
Natural coagulation inhibitor proteins in young patients with cerebral ischemia
CEREBROVASCULAR DISEASES
Modification of the ProC (R) Global assay using dilution of patient plasmain factor V-depleted plasma as a screening assay for factor V Leiden mutation
BLOOD COAGULATION & FIBRINOLYSIS
Activated protein C resistance and false type 2 protein C deficiency detected after multiple shunt failures in a patient with hydrocephalus
JOURNAL OF CHILD NEUROLOGY
The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
Update on selected inherited venous thrombotic disorders
AMERICAN JOURNAL OF HEMATOLOGY
Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism - Pooled analysis of 8 case-control studies including2310 cases and 3204 controls
THROMBOSIS AND HAEMOSTASIS
Risk factors in venous thromboembolism
THROMBOSIS AND HAEMOSTASIS
The epidemiology of venous thromboembolism in the community
THROMBOSIS AND HAEMOSTASIS
Factor X levels, polymorphisms in the promoter region of factor X, and therisk of venous thrombosis
THROMBOSIS AND HAEMOSTASIS
Factor V Arg(306)-> Gly mutation is not associated with activated protein C resistance and is rare in Taiwanese Chinese
THROMBOSIS AND HAEMOSTASIS
Functional properties of factor V and factor Va encoded by the R2-gene
THROMBOSIS AND HAEMOSTASIS
Oral contraceptives, thrombosis and haemostasis
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY
HELLP syndrome and factor V Leiden
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY
Factor V-LEIDEN and cardiopulmonary bypass: investigation of haemostatic parameters and the effect of aprotinin using an ex vivo model
PERFUSION-UK
Sensitivity of the ProC((R)) global assay for protein C pathway abnormalities. Clinical experience in 899 unselected patients with venous thromboembolism
THROMBOSIS RESEARCH
Interaction of fibrinolysis and prothrombotic risk factors in neonates, infants and children with and without thromboembolism and underlying cardiac disease - A prospective study
THROMBOSIS RESEARCH
The role of protein C, protein S, and resistance to activated protein C inLegg-Perthes disease
PEDIATRICS
Advances in the genetics of cerebrovascular disease and stroke
NEUROLOGY
Hormone replacement therapy and acquired resistance to activated protein C: results of a randomized, double-blind, placebo-controlled trial
BRITISH JOURNAL OF HAEMATOLOGY
Investigation and management of heritable thrombophilia
BRITISH JOURNAL OF HAEMATOLOGY
Genetic hypercoagulability: prevention suggests testing family members
BLOOD
An update on hypercoagulable disorders
ARCHIVES OF INTERNAL MEDICINE
The thrombophilias: Well-defined risk factors with uncertain therapeutic implications
ANNALS OF INTERNAL MEDICINE
The thrombophilic state in cancer patients
ACTA HAEMATOLOGICA
The impact of the Factor V Leiden mutation on pregnancy
HUMAN REPRODUCTION UPDATE
Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylenetetrahydrofolate reductase polymorphisms in pregnancy
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Combined heterozygous plasminogen deficiency and factor V Leiden defect inthe same kindred
CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
Hereditary and acquired thrombophilia
SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE
DNA technology for the detection of common genetic variants that predispose to thrombophilia
BLOOD COAGULATION & FIBRINOLYSIS
Comparison of thrombotic risk between 85 homozygotes and 481 heterozygotescarriers of the factor V Leiden mutation: retrospective analysis from the Procare Study
BLOOD COAGULATION & FIBRINOLYSIS
Multiple analysis of three common genetic alterations associated with thrombophilia
BLOOD COAGULATION & FIBRINOLYSIS
Predictors of left ventricular thrombus formation in patients with anterior myocardial infarction: role of activated protein C resistance
CORONARY ARTERY DISEASE
Activated protein C resistance in Budd-Chiari syndrome
INTERNATIONAL JOURNAL OF HEMATOLOGY
Resistance to activated protein C and FV Leiden mutation in patients with a history of acute myocardial infarction or primary hypertension
AMERICAN JOURNAL OF HYPERTENSION
Factor V Leiden and prothrombin G20210A - Demystifying two common genetic predispositions to venous thrombosis
CLEVELAND CLINIC JOURNAL OF MEDICINE
Upper extremity deep venous thrombosis: An underrecognized manifestation of a hypercoagulable state
ANNALS OF VASCULAR SURGERY
The caput medusae of hypercoagulability
JOURNAL OF VASCULAR SURGERY
The prevalence of Factor V Leiden as a risk factor for venous thromboembolism in the population of North-Western Greece
INTERNATIONAL ANGIOLOGY
Recurrent venous thrombosis and markers of inflammation
THROMBOSIS AND HAEMOSTASIS
The HR2 haplotype of factor V: Effects on factor V levels, normalized activated protein C sensitivity ratios and the risk of venous thrombosis
THROMBOSIS AND HAEMOSTASIS
The factor V R2 allele: Risk of venous thromboembolism, factor V levels and resistance to activated protein C
THROMBOSIS AND HAEMOSTASIS
Significantly increased prevalence of factor V Leiden in patients with dural arteriovenous fistulas
JOURNAL OF NEUROLOGY
The molecular mechanisms of inherited thrombophilia
ZEITSCHRIFT FUR KARDIOLOGIE
Simultaneous occurrence of autoimmune enteropathy and recurrent deep venous thrombosis
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
Abdominal nodules as a presentation of obstruction of the inferior vena cava and factor V Leiden mutation
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
Blood coagulation
LANCET
Thrombosis and cancer
SEMINARS IN ONCOLOGY
Frequency of polymorphisms in the B-domain of factor V gene in APC-resistant patients
THROMBOSIS RESEARCH
Sudden infant death syndrome, childhood thrombosis, and presence of genetic risk factors for thrombosis
THROMBOSIS RESEARCH
The molecular basis of inherited thrombophilia
VOX SANGUINIS
Factor V R506Q mutation (activated protein C resistance) is an additional risk factor for early renal graft loss associated with acute vascular rejection
TRANSPLANTATION
Obstetric implications of activated protein C resistance and factor V leiden Mutation
OBSTETRICAL & GYNECOLOGICAL SURVEY
Hereditary thrombophilias in ischemic stroke and sinus vein thrombosis: diagnostic, therapy and meta-analysis
NERVENARZT
Thrombophilia in pregnancy
JOURNAL OF CLINICAL PATHOLOGY
The risk of venous thromboembolism in family members with mutations in thegenes of factor V or prothrombin or both
BRITISH JOURNAL OF HAEMATOLOGY
Factor XIII Va134Leu and the risk of venous thromboembolism in factor V Leiden carriers
BRITISH JOURNAL OF HAEMATOLOGY
Combined genetic defect (homogeneity for factor V Leiden and heterogeneityfor prothrombin G20210A allele), in a young patient, with recurrent deep vein thrombosis and serious postphlebitic syndrome - A case report
ANGIOLOGY
Role of activated protein C resistance in left atrial thrombogenesis in patients with mitral stenosis
ANGIOLOGY
Cardiovascular implications of the factor V Leiden mutation
AMERICAN HEART JOURNAL
The Bavarian thromboembolie risk cohort study(BATER)
DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT
The molecular genetics of familial venous thrombosis
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
Risk of venous thromboembolism and clinical manifestations in carriers of antithrombin, protein C, protein S deficiency, or activated protein C resistance - A multicenter collaborative family study
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Study of the prothrombin gene 20201 GA variant in FV : Q(506) carriers in relationship to the presence or absence of juvenile venous thromboembolism
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Prothrombin G20210A gene mutation and further prothrombotic risk factors in childhood thrombophilia
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Functional activated protein C resistance assays: correlation with factor V DNA analysis is better with RVVT- than APTT-based assays
BRITISH JOURNAL OF BIOMEDICAL SCIENCE
Recent advances in haematology
BRITISH MEDICAL JOURNAL
Lack of association between factor V Leiden and thromboembolism in patients with prosthetic heart valves
BLOOD COAGULATION & FIBRINOLYSIS
Activated protein C ratio as a clue for protein S disorder in Japanese
BLOOD COAGULATION & FIBRINOLYSIS
Careful selection of sample dilution and factor-V-deficient plasma makes the modified activated protein C resistance test highly specific for the factor V Leiden mutation
BLOOD COAGULATION & FIBRINOLYSIS
Prevalence of APC resistance and its relationship to arterial and venous thromboembolism in a general population sample of elderly Swedish men: The Study of Men Born in 1913
JOURNAL OF INTERNAL MEDICINE
Activated protein C resistance in patients with central retinal vein occlusion in comparison to patients with a history of deep-vein thrombosis and ahealthy control group
OPHTHALMOLOGE
Clinical importance and evidence of APC-resistance
PHLEBOLOGIE
Genetic risk factors for phlebothrombosis: New aspects under special consideration of the inherited resistance to activated protein C (coagulation factor V Leiden).
PERFUSION
Diagnosis and management of inherited and acquired thrombophilias
JOURNAL OF THROMBOSIS AND THROMBOLYSIS
Venous thromboembolism, factor V Leiden, and methylenetetrahydrofolate reductase in a sickle cell anemia patient
PEDIATRIC HEMATOLOGY AND ONCOLOGY
Patients with venous thromboembolism have a lower APC response than controls. Should this be regarded as a continuous risk factor for venous thrombosis?
HAEMATOLOGICA
Thrombophilia as a multigenic disease
HAEMATOLOGICA
Coagulation factor V Leiden mutation in sudden fatal pulmonary embolism and in a general northern European population sample
FORENSIC SCIENCE INTERNATIONAL
Allelic discrimination of factor V Leiden using a 5 ' nuclease assay
THROMBOSIS AND HAEMOSTASIS
Molecular risk factors for thrombosis
THROMBOSIS AND HAEMOSTASIS
Risk factors for venous thrombotic disease
THROMBOSIS AND HAEMOSTASIS
The risk of recurrent venous thromboembolism in carriers and non-carriers of the G1691A allele in the coagulation factor V gene and the G20210A allele in the prothrombin gene
THROMBOSIS AND HAEMOSTASIS
Factor V Leiden, prothrombin 20210 G -> A and the MTHFR C677T mutations inchildhood stroke
THROMBOSIS AND HAEMOSTASIS
Activated protein C (APC) resistance in young stroke patients
THROMBOSIS AND HAEMOSTASIS
The factor V gene A4070G mutation and the risk of venous thrombosis
THROMBOSIS AND HAEMOSTASIS
Incidence of venous thromboembolism in families with inherited thrombophilia
THROMBOSIS AND HAEMOSTASIS
Near-infrared spectroscopy monitored cerebral venous thrombolysis
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
Risk of thrombosis in patients with antiphospholipid antibodies and factorV Leiden mutation
JOURNAL OF RHEUMATOLOGY
Clinical aspects and laboratory problems in hereditary thrombophilia
HAEMOSTASIS
Venous thrombosis: Prevalence and interaction of risk factors
HAEMOSTASIS
Haemostatic and metabolic abnormalities in women with unexplained recurrent abortion
HUMAN REPRODUCTION
Low-dose oral contraceptives and acquired resistance to activated protein C: a randomised cross-over study
LANCET
Venous thrombosis: a multicausal disease
LANCET
Detection of decreased response to activated protein C during pregnancy byan endogenous thrombin potential-based assay
SEMINARS IN THROMBOSIS AND HEMOSTASIS
Treatment of hereditary and acquired thrombophilic disorders
SEMINARS IN THROMBOSIS AND HEMOSTASIS
Activated protein C resistance and thrombosis: Molecular mechanisms of hypercoagulable state due to FVR506Q mutation
SEMINARS IN THROMBOSIS AND HEMOSTASIS