(Q44426328)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12725943%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Large volume donor plasmapheresis in inherited thrombophilia implicated in arterial thrombosis (English)

1 reference

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3 November 2019

1 reference

1 reference

6

1 reference

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3 November 2019

3

Mehmet Ozmenoglu

1 reference

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3 November 2019

author name string

Ercüment Ovali

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12725943%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Siret Ratip

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12725943%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

S Sami Karti

4

1 reference

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3 November 2019

Fahri Uçar

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12725943%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Mustafa Yilmaz

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12725943%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Polat Koşucu

8

1 reference

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3 November 2019

publication date

1 June 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12725943%20AND%20SRC:MED&resulttype=core&format=json

Transfusion and Apheresis Science

3 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12725943%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

28

1 reference

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3 November 2019

issue

3

1 reference

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3 November 2019

page(s)

201-206

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12725943%20AND%20SRC:MED&resulttype=core&format=json

Frequency of immediate adverse effects associated with apheresis donation

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Three years with a national apheresis registry

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Determination of free and total homocysteine in human plasma by high-performance liquid chromatography with fluorescence detection

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

A novel ELISA-based primer extension assay for the detection of the factor V Leiden mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Potential danger of thrombosis after plasma exchange in the treatment of patients with immune disease

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

The hemostatic system in children undergoing intensive plasma exchange

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Decrease and rapid recovery of protein C after plasma exchange

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Effects of intensive plasmapheresis on the haemostatic system

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Molecular variant of 5,10-methylenetetrahydrofolate reductase is a risk factor of ischemic heart disease in the Japanese population

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Prevalence of methylenetetrahydrofolate reductase C677T and its association with arterial and venous thrombosis in the Chinese population

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Ischemic stroke in a young patient with protein C deficiency and prothrombin gene mutation G20210A.

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

Homozygous Prothrombin Gene Mutationand Ischemic Cerebrovascular Disease

1 reference

https://api.crossref.org/works/10.1016%2FS1473-0502%2803%2900054-5

7 January 2021

10.1016/S1473-0502(03)00054-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12725943%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference