Prevalence of the factor V leiden mutation in children and neonates with thromboembolic disease (Q62754959)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842043%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

title

Prevalence of the factor V leiden mutation in children and neonates with thromboembolic disease (English)

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7 December 2019

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5

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7 December 2019

author name string

J N Hagstrom

1

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7 December 2019

J Walter

2

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7 December 2019

R Bluebond-Langner

3

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7 December 2019

J C Amatniek

4

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7 December 2019

K A High

6

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7 December 2019

language of work or name

English

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publication date

1 December 1998

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The Journal of Pediatrics

7 December 2019

published in

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7 December 2019

volume

133

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7 December 2019

page(s)

777-781

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7 December 2019

issue

6

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Venous thromboembolic complications in children

7 December 2019

cites work

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7 January 2021

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Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study

7 January 2021

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Factor V Leiden (FVQ 506) is common in a Brazilian population.

7 January 2021

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High prevalence of a mutation in the factor V gene within the U.K. population: relationship to activated protein C resistance and familial thrombosis.

7 January 2021

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Activated protein C resistance in cases of cerebral infarction.

7 January 2021

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Reduced response to activated protein C is associated with increased risk for cerebrovascular disease.

7 January 2021

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Myocardial infarction, Arg 506 to Gln factor V mutation, and activated protein C resistance.

7 January 2021

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

7 January 2021

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Thrombosis in otherwise well children with the factor V Leiden mutation

7 January 2021

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APC resistance in childhood thromboembolism: diagnosis and clinical aspects

7 January 2021

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Resistance to activated protein C (APCR) in children with venous or arterial thromboembolism

7 January 2021

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Prevalence of factor V Leiden in children with thrombo-embolism

7 January 2021

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The G1691A mutation of the coagulation factor V gene (factor V Leiden) is rare in Chinese: an analysis of 618 individuals

7 January 2021

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Childhood stroke associated with protein C or S deficiency and primary antiphospholipid syndrome.

7 January 2021

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Childhood stroke associated with familial protein S deficiency.

7 January 2021

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Activated protein C resistance in childhood stroke

7 January 2021

1 reference

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10.1016/S0022-3476(98)70150-7

7 January 2021

Identifiers

DOI

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7 December 2019

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