(Q28171246)

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Ramifications of four concurrent thrombophilic mutations and one hypofibrinolytic mutation

scientific article (publication date: October 2004)

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Ramifications of four concurrent thrombophilic mutations and one hypofibrinolytic mutation (English)

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Charles J Glueck

1

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Naila Goldenberg

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2

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Ping Wang

series ordinal

3

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Dawit Aregawi

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4

0 references

language of work or name

English

0 references

publication date

October 2004

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published in

Clinical and Applied Thrombosis-Hemostasis

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volume

10

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issue

4

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page(s)

365-71

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cites work

Venous thromboembolism epidemiology: implications for prevention and management

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21 January 2018

Principle mechanisms underlying venous thromboembolism: epidemiology, risk factors, pathophysiology and pathogenesis

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21 January 2018

Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment

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21 January 2018

Risk of venous thromboembolism in carriers of factor V Leiden with a concomitant inherited thrombophilic defect: a retrospective analysis.

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21 January 2018

Idiopathic intracranial hypertension: associations with coagulation disorders and polycystic-ovary syndrome

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21 January 2018

Relationships between lipoprotein(a), lipids, apolipoproteins, basal and stimulated fibrinolytic regulators, and D-dimer.

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21 January 2018

Increased frequency of genetic thrombophilia in women with complications of pregnancy

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21 January 2018

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

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21 January 2018

Effect of oral and transdermal estrogen replacement therapy on hemostatic variables associated with venous thrombosis: a randomized, placebo-controlled study in postmenopausal women

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21 January 2018

The platelet Pl(A2) and angiotensin-converting enzyme (ACE) D allele polymorphisms and the risk of recurrent events after acute myocardial infarction

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21 January 2018

Polycystic ovary syndrome, the G1691A factor V Leiden mutation, and plasminogen activator inhibitor activity: associations with recurrent pregnancy loss

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21 January 2018

PAI-1 gene 4G/5G genotype: A risk factor for thrombosis in vessels of internal organs

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21 January 2018

Major and potential prothrombotic genotypes in a cohort of patients with venous thromboembolism

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21 January 2018

Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease

1 reference

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Crossref

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21 January 2018

Heterogeneity in the prevalence of methylenetetrahydrofolate reductase gene polymorphisms in women of different ethnic groups

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21 January 2018

Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos

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21 January 2018

Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction

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21 January 2018

Ximelagatran versus warfarin for stroke prevention in patients with nonvalvular atrial fibrillation. SPORTIF II: a dose-guiding, tolerability, and safety study

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21 January 2018

Impact of the factor II: G20210A variant on the risk of venous thromboembolism in relatives from families with the factor V: R506Q mutation

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21 January 2018

Identifiers

DOI

10.1177/107602960401000409

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PubMed publication ID

15497023

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(Q28171246)

Ramifications of four concurrent thrombophilic mutations and one hypofibrinolytic mutation

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