(Q46784491)

English

Budd-Chiari syndrome with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations

scientific article published in October 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

Budd-Chiari syndrome with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

Factor V Leiden

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

author name string

Kassem A Barada

1

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

Cecilio R Azar

2

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

Zaher K Otrock

3

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

publication date

1 October 2005

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

Journal of Gastroenterology

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

40

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

10

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

1002-1003

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

Prevalence of the factor V Leiden mutation in hepatic and portal vein thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16261441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liver transplantation in a patient with Budd-Chiari syndrome secondary to factor V Leiden mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16261441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden related Budd-Chiari syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16261441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Budd-Chiari syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16261441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Budd-Chiari syndrome related to factor V Leiden mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16261441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma homocysteine as a risk factor for vascular disease. The European Concerted Action Project.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16261441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16261441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited thrombophilia: resistance to activated protein C as a pathogenic factor of venous thromboembolism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16261441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00535-005-1664-2

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/16261441

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