High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. (Q31987604)

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4 November 2019

title

High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis (English)

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4 November 2019

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4

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4 November 2019

author name string

Amitrano L

1

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4 November 2019

Brancaccio V

2

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4 November 2019

Guardascione MA

3

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4 November 2019

Iannaccone L

5

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4 November 2019

Dandrea G

6

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4 November 2019

Ames PR

7

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4 November 2019

Marmo R

8

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Mosca S

9

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Balzano A

10

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language of work or name

English

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publication date

1 January 2001

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The American Journal of Gastroenterology

4 November 2019

published in

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volume

96

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issue

1

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page(s)

146-149

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Mutation in blood coagulation factor V associated with resistance to activated protein C.

4 November 2019

cites work

1 reference

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

21 January 2018

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Hyperhomocysteinemia as a risk factor for deep-vein thrombosis.

21 January 2018

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The Arg506Gln mutation (FV Leiden) among a cohort of 4188 unselected Danish newborns

21 January 2018

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The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels

21 January 2018

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Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine and other risk factors for vascular disease.

21 January 2018

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Mesenteric vein thrombosis due to factor V Leiden gene mutation.

21 January 2018

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Portal and mesenteric vein thrombosis in a patient heterozygous for a mutation (Arg506-->Gln) in the factor V gen (factor V Leiden).

21 January 2018

1 reference

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Factor II 20210 G-->A polymorphism associated to factor V Leiden: a report of two thrombophilic families.

21 January 2018

1 reference

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Mesenteric venous thrombosis

21 January 2018

1 reference

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Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3'-untranslated region of the prothrombin gene

21 January 2018

1 reference

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Effect of the MTHFRC677T variant on risk of venous thromboembolism: interaction with factor V Leiden and prothrombin (F2G20210A) mutations

21 January 2018

1 reference

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Inherited prothrombotic risk factors and cerebral venous thrombosis

21 January 2018

1 reference

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Budd-Chiari syndrome, portal vein and mesenteric vein thrombosis in a patient homozygous for factor V Leiden mutation treated by TIPS and thrombolysis

21 January 2018

1 reference

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21 January 2018

Identifiers

DOI

1 reference

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4 November 2019

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