(Q41850472)

English

Thrombophilic Genetic Factors PAI-1, MTHFRC677T, V Leiden 506Q, and Prothrombin 20210A in Noncirrhotic Portal Vein Thrombosis and Budd-Chiari Syndrome in a Caucasian Population

scientific article published on 18 December 2013

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Thrombophilic Genetic Factors PAI-1, MTHFRC677T, V Leiden 506Q, and Prothrombin 20210A in Noncirrhotic Portal Vein Thrombosis and Budd-Chiari Syndrome in a Caucasian Population (English)

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

portal vein thrombosis

1 reference

based on heuristic

inferred from title

author name string

Mario D'Amico

1

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Pietro Sammarco

2

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Linda Pasta

3

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

publication date

18 December 2013

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

International Journal of Vascular Medicine

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

2013

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

717480

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

copyright license

Creative Commons Attribution 3.0 Unported

1 January 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

Hepatic endothelial dysfunction and abnormal angiogenesis: new targets in the treatment of portal hypertension.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

5 June 2018

Portal vein thrombosis and budd-Chiari syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

5 June 2018

Hardy-Weinberg equilibrium testing of biological ascertainment for Mendelian randomization studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

5 June 2018

The role of thrombophilia in splanchnic vein thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

5 June 2018

Risk factors of thrombosis in abdominal veins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

5 June 2018

The effect of the plasminogen activator inhibitor-1 4G/5G polymorphism on the thrombotic risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

5 June 2018

Folate and choline metabolism gene variants and development of uterine cervical carcinoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

18 August 2018

Prognostic value of pre-surgical plasma PAI-1 (plasminogen activator inhibitor-1) levels in breast cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

18 August 2018

MTHFR C677TT, PAI1 4G-4G, V Leiden Q506, and prothrombin G20210A in hepatocellular carcinoma with and without portal vein thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

18 August 2018

MTHFR C677T mutations in liver cirrhosis with and without portal vein thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

18 August 2018

Methylenetetrahydrofolate reductase (MTHFR) and susceptibility for (pre)neoplastic cervical disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

18 August 2018

Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis: a study from North India

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

18 August 2018

Methylenetetrahydrofolate reductase polymorphism C677T is not associated to the risk of cervical dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

18 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3880691

18 August 2018

Etiology, Management, and Outcome of the Budd-Chiari Syndrome

1 reference

https://api.crossref.org/works/10.1155%2F2013%2F717480

21 January 2018

Portal vein thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/24455271

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk factors for thrombophilia in extrahepatic portal vein obstruction

1 reference

https://pubmed.ncbi.nlm.nih.gov/24455271

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis: results of a case-control study

1 reference

https://pubmed.ncbi.nlm.nih.gov/24455271

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1155/2013/717480

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

ResearchGate publication ID

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