(Q43588765)

25 November 2017

Common mutations at the homocysteine metabolism pathway and pediatric stroke (English)

1 reference

25 November 2017

Akar N

1

1 reference

25 November 2017

Akar E

2

1 reference

25 November 2017

Ozel D

3

1 reference

25 November 2017

Deda G

4

1 reference

25 November 2017

Sipahi T

5

1 reference

25 November 2017

1 April 2001

1 reference

25 November 2017

1 reference

25 November 2017

102

1 reference

25 November 2017

2

1 reference

25 November 2017

115-120

1 reference

Stroke in children within a major metropolitan area: the surprising importance of intracerebral hemorrhage

25 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

Etiology of stroke in children

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

Cerebrovascular disorders of childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

Factor V1691 G-A, prothrombin 20210 G-A, and methylenetetrahydrofolate reductase 677 C-T variants in Turkish children with cerebral infarct

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

Factor V Leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

Hyperhomocysteinemia: an independent risk factor for vascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

Hyperhomocysteinemia as a risk factor for deep-vein thrombosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

A rapid screening method for the factor V Arg506-->Gln mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

Prothrombin gene 20210 G-A mutation in the Turkish population.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900226-2

7 January 2021

10.1016/S0049-3848(01)00226-2

Identifiers

DOI

1 reference

25 November 2017

1 reference