Evaluation of the modifying effects of unfavourable genotypes on classical clinical risk factors for ischaemic stroke (Q35560338)

8 August 2017

Evaluation of the modifying effects of unfavourable genotypes on classical clinical risk factors for ischaemic stroke (English)

1 reference

8 August 2017

Szolnoki Z

1

1 reference

8 August 2017

Somogyvári F

2

1 reference

8 August 2017

Kondacs A

3

1 reference

8 August 2017

Szabó M

4

1 reference

8 August 2017

Fodor L

5

1 reference

8 August 2017

Bene J

6

1 reference

8 August 2017

Melegh B

7

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 December 2003

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

8 August 2017

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8 August 2017

74

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8 August 2017

12

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8 August 2017

1615-1620

1 reference

Evaluation of the roles of common genetic mutations in leukoaraiosis

8 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Genetics and ischaemic stroke

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Role of a common mutation in the homocysteine regulatory enzyme methylenetetrahydrofolate reductase in ischemic stroke.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

An angiotensin-converting enzyme gene polymorphism suggests a genetic distinction between ischaemic stroke and carotid stenosis.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Genetic susceptibility and ischaemic stroke

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Protein S deficiency, activated protein C resistance and sticky platelet syndrome in a young woman with bilateral strokes.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Is hormone replacement a risk factor for ischemic stroke in women with factor V Leiden mutation?

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Factor V Leiden mutation in a case with ischemic stroke: which relationship? A case report.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

The inherited basis of venous thrombosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Polymorphism of the angiotensin-converting enzyme (ACE) gene in patients with thrombotic brain infarction.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Lack of association between angiotensin converting enzyme gene insertion/deletion polymorphism and stroke.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Apolipoprotein E polymorphism and ischemic cerebrovascular disease.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

World distribution of factor V Leiden

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Evaluation of the roles of the Leiden V mutation and ACE I/D polymorphism in subtypes of ischaemic stroke.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Lack of association between apolipoprotein E genoype and ischaemic stroke in a Scottish population.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Apolipoprotein E genetic polymorphism and stroke subtypes in a Bangladeshi hospital-based study.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Polymorphism of apoprotein E (APOE), methylenetetrahydrofolate reductase (MTHFR) and paraoxonase (PON1) genes in patients with cerebrovascular disease

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Common genetic mutations as possible aetiological factors in stroke

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Evaluation of genetic risk factors for silent brain infarction.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Thrombophilic predisposition in stroke and venous thromboembolism in Danish patients.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Genetic analysis of the thermolabile variant of 5, 10-methylenetetrahydrofolate reductase as a risk factor for ischemic stroke.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: a case-control study.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Factor V Leiden and prothrombin gene G 20210 A variant in children with ischemic stroke.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Prevalence of factor V Leiden mutation in young adults with cerebral ischaemia: a case-control study on 225 patients.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

ACE gene polymorphism as a risk factor for ischemic cerebrovascular disease.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Alternative PCR method for diagnosis of mutation causing activated protein C resistant Gln506-factor V.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757435

Interaction of heritable and estrogen-induced thrombophilia: possible etiologies for ischemic optic neuropathy and ischemic stroke

26 September 2018

1 reference

12 December 2020

Real-time PCR assay with fluorescent hybridization probes for exact and rapid genotyping of the angiotensin-converting enzyme gene insertion/deletion polymorphism

1 reference

12 December 2020

Apolipoprotein E ε4 Allele in Alzheimer's Disease and Vascular Dementia

1 reference

12 December 2020

Single-day apolipoprotein E genotyping

1 reference

12 December 2020

Factor V Leiden gene mutation and thrombin generation in relation to the development of acute stroke

1 reference

12 December 2020

Angiotensin-converting enzyme gene deletion polymorphism. A new risk factor for lacunar stroke but not carotid atheroma

1 reference

12 December 2020

Arg506Gln factor V mutation (factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction

1 reference

12 December 2020

Age-specific incidence rates of venous thromboembolism among heterozygous carriers of factor V Leiden mutation

1 reference

12 December 2020

Reliable genotyping of the G-20210-A mutation of coagulation factor II (prothrombin)

1 reference

12 December 2020

Risk of stroke in young women and two prothrombotic mutations: factor V Leiden and prothrombin gene variant (G20210A)

1 reference

12 December 2020

Methylenetetrahydrofolate reductase gene polymorphism Relation to blood pressure and cerebrovascular disease

1 reference

12 December 2020

Arterial thromboembolic events in patients with the factor V Leiden mutation

1 reference

12 December 2020

Factor V Leiden, prothrombin 20210G-->A and the MTHFR C677T mutations in childhood stroke

1 reference

12 December 2020

Association of elevated levels of prothrombin fragment 1+2 and Arg506 to Gln mutation in patients with a history of ischemic stroke

1 reference

12 December 2020

Genotyping method for methylenetetrahydrofolate reductase (C677T thermolabile variant) using heteroduplex technology

1 reference

12 December 2020

Factor V Leiden mutation is a risk factor for cerebral venous thrombosis: a case-control study of 55 patients

1 reference

12 December 2020

Prospective evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of stroke

1 reference

12 December 2020

Methylene tetrahydrofolate reductase C677T genotype and stroke

1 reference

12 December 2020

G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men

1 reference

12 December 2020

Hereditary thrombophilia in cerebral venous thrombosis.

1 reference

12 December 2020

Gene polymorphism of the renin-angiotensin system associates with risk for lacunar infarction. The Ohasama study

1 reference

12 December 2020

Screening for thrombophilic risk factors among 25 German patients with cerebral venous thrombosis

1 reference

12 December 2020

A clustering of unfavourable common genetic mutations in stroke cases

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.74.12.1615

1 reference

8 August 2017

1 reference

8 August 2017

1 reference