Haemostatic genetic variants, ABO blood group and bleeding risk during oral anticoagulant treatment after cerebral ischaemia of arterial origin (Q46906726)

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scientific article published on 14 November 2007

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English	Haemostatic genetic variants, ABO blood group and bleeding risk during oral anticoagulant treatment after cerebral ischaemia of arterial origin	scientific article published on 14 November 2007

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

Haemostatic genetic variants, ABO blood group and bleeding risk during oral anticoagulant treatment after cerebral ischaemia of arterial origin (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

cerebral infarction

1 reference

based on heuristic

inferred from title

anticoagulation

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based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

6

object named as

A Algra

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

author name string

D M O Pruissen

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

F R Rosendaal

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

J W Gorter

3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

A A Garcia

4

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

L J Kappelle

5

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

SPIRIT Study Group

7

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

publication date

14 November 2007

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

254

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Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

12

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

1660-1665

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

Major bleeding during anticoagulation after cerebral ischemia: patterns and risk factors. Stroke Prevention In Reversible Ischemia Trial (SPIRIT). European Atrial Fibrillation Trial (EAFT) study groups

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0609-5

21 January 2018

Antithrombotic therapy to prevent stroke in patients with atrial fibrillation: a meta-analysis

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0609-5

21 January 2018

Factor V Leiden and the risk for venous thromboembolism in the adult Danish population

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0609-5

21 January 2018

Clinical impact of bleeding in patients taking oral anticoagulant therapy for venous thromboembolism: a meta-analysis

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0609-5

21 January 2018

Two common, functional polymorphisms in the promoter region of the beta-fibrinogen gene contribute to regulation of plasma fibrinogen concentration

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0609-5

21 January 2018

The relationship between ABO blood group and the risk of bleeding during vitamin K antagonist treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein E genotype and cerebral amyloid angiopathy-related hemorrhage

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic regulation of fibrin structure and function: complex gene-environment interactions may modulate vascular risk.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of coagulation factor XIII subunit A and risk of nonfatal hemorrhagic stroke in young white women

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antiplatelet and anticoagulation for patients with prosthetic heart valves

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing to hereditary thrombophilia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A randomized trial of anticoagulants versus aspirin after cerebral ischemia of presumed arterial origin. The Stroke Prevention in Reversible Ischemia Trial (SPIRIT) Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel polymorphism in the factor XIII B-subunit (His95Arg): relationship to subunit dissociation and venous thrombosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of the fibrinogen Aalpha Thr312Ala polymorphism: effects on fibrin structure and function.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased prevalence of factor V Leiden mutation in premature but not in full-term infants with grade I intracranial haemorrhage

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of warfarin and aspirin for symptomatic intracranial arterial stenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interactions between thrombophilic genetic mutations and clinical bleeding in patients on chronic oral anticoagulant treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V and thrombotic disease: description of a janus-faced protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Grading white matter lesions on CT and MRI: a simple scale

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor XIII Val34Leu polymorphism and gamma-chain cross-linking at the site of microvascular injury in healthy and coumadin-treated subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A C1173T dimorphism in the VKORC1 gene determines coumarin sensitivity and bleeding risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oral anticoagulant therapy in patients with coronary artery disease: a meta-analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of clotting factors modify the risk for primary intracranial hemorrhage

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic discrimination using fluorogenic probes and the 5' nuclease assay

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patients with an ApoE epsilon4 allele require lower doses of coumarin anticoagulants

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comparison of warfarin and aspirin for the prevention of recurrent ischemic stroke

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Does apolipoprotein E genotype influence the risk of ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage? Systematic review and meta-analyses of 31 studies among 5961 cases and 17,965 controls.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Leu564 factor XIIIA variant results in significantly lower plasma factor XIII levels than the Pro564 variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secondary prevention in non-rheumatic atrial fibrillation after transient ischaemic attack or minor stroke. EAFT (European Atrial Fibrillation Trial) Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased risk of intraventricular hemorrhage in preterm infants with thrombophilia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Medium intensity oral anticoagulants versus aspirin after cerebral ischaemia of arterial origin (ESPRIT): a randomised controlled trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of Val34Leu polymorphism on the activation of the coagulation factor XIII-A

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three months versus one year of oral anticoagulant therapy for idiopathic deep venous thrombosis. Warfarin Optimal Duration Italian Trial Investigators

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prothrombotic factors in neonates with cerebral thrombosis and intraventricular hemorrhage.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Seven haemostatic gene polymorphisms in coronary disease: meta-analysis of 66,155 cases and 91,307 controls.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype/phenotype correlations for coagulation factor XIII: specific normal polymorphisms are associated with high or low factor XIII specific activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome P450 2C9 (CYP2C9) and vitamin K epoxide reductase (VKORC1) genotypes as determinants of acenocoumarol sensitivity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anticoagulants versus antiplatelet therapy for preventing stroke in patients with nonrheumatic atrial fibrillation and a history of stroke or transient ischemic attack

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid and simple ABO genotype screening method using a novel B/O2 versus A/O2 discriminating nucleotide substitution at the ABO locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994314

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00415-007-0609-5

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17994314

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