(Q50957387)

26 March 2018

title

Genetic prothrombotic mutations are common in neonates but are not associated with umbilical catheter-associated thrombosis. (English)

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26 March 2018

main subject

thrombosis

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author

Satyan Lakshminrusimha

5

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26 March 2018

author name string

Turebylu R

1

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26 March 2018

Salis R

2

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26 March 2018

Erbe R

3

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26 March 2018

Martin D

4

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26 March 2018

Ryan RM

6

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26 March 2018

publication date

12 July 2007

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26 March 2018

published in

Journal of Perinatology

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26 March 2018

volume

27

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26 March 2018

issue

8

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26 March 2018

page(s)

490-495

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26 March 2018

https://scigraph.springernature.com/pub.10.1038/sj.jp.7211786

exact match

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cites work

Umbilical artery catheterization in the newborn

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

Aortic thrombosis after umbilical artery catheterization

21 January 2018

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Resistance to activated protein C, the FV:Q506 allele, and venous thrombosis

21 January 2018

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The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

Ethnic distribution of factor V Leiden in 4047 men and women. Implications for venous thromboembolism screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

The 1298A-->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

Prevalence of moderate hyperhomocysteinemia in patients with early-onset venous and arterial occlusive disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

5,10-Methylenetetrahydrofolate reductase polymorphisms and leukemia risk: a HuGE minireview

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

Umbilical arterial catheter use: report of an audit conducted by the Study Group for Complications of Perinatal Care

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Risk factors associated with umbilical vascular catheter-associated thrombosis in newborn infants

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Sonographic detection of neonatal umbilical-artery thrombosis: clinical correlation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Aortic thrombosis after umbilical artery catheterization in neonates: prevalence of complications on long-term follow-up

1 reference

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7 January 2021

Endovascular treatment of renal artery thrombosis caused by umbilical artery catheterization

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Does umbilical vein catheterization lead to portal venous thrombosis? Prospective US evaluation in 100 neonates

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Umbilical vessel catheterization: indications, management, and evaluation of the technique

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Factor V Leiden, protein C, and lipoprotein (a) in catheter-related thrombosis in childhood: a prospective study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Factor V Leiden in central venous catheter-associated thrombosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Symptomatic ischemic stroke in full-term neonates : role of acquired and genetic prothrombotic risk factors

1 reference

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7 January 2021

Prothrombin G20210A gene mutation and further prothrombotic risk factors in childhood thrombophilia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Ultrasonic detection of complications following umbilical arterial catheterization in the neonate

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Do umbilical vein catheterization and sepsis lead to portal vein thrombosis? A prospective, clinical, and sonographic evaluation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Severe aortic thrombosis in the neonate--successful treatment with low-molecular-weight heparin: two case reports and review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Effect of heparin infusates in umbilical arterial catheters on frequency of thrombotic complications

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Umbilical catheterization: its complications. Anatomical study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Study of the prothrombin gene 20201 GA variant in FV:Q506 carriers in relationship to the presence or absence of juvenile venous thromboembolism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

The procoagulant effects of factor V Leiden may be balanced against decreased levels of factor V and do not reflect in vivo thrombin formation in newborns

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JP.7211786

7 January 2021

Identifiers

DOI

10.1038/SJ.JP.7211786

1 reference

26 March 2018

1 reference

26 March 2018