Methylenetetrahydrofolate reductase gene polymorphisms and cerebral palsy in Chinese infants. (Q51832667)

13 April 2018

title

Methylenetetrahydrofolate reductase gene polymorphisms and cerebral palsy in Chinese infants. (English)

1 reference

13 April 2018

1 reference

Xiuyong Cheng

1

1 reference

13 April 2018

Tongchuan Li

2

1 reference

13 April 2018

Honglian Wang

3

1 reference

13 April 2018

Dengna Zhu

4

1 reference

13 April 2018

Caiyun Ma

5

1 reference

13 April 2018

Bingxiang Ma

6

1 reference

13 April 2018

Yinghong Wang

7

1 reference

13 April 2018

Junyu Zhang

8

1 reference

13 April 2018

Luo Guo

9

1 reference

13 April 2018

Lei Wang

10

1 reference

13 April 2018

Liu Yun

11

1 reference

13 April 2018

Shiting Chen

12

1 reference

13 April 2018

Zedong Jiang

13

1 reference

13 April 2018

Lin He

14

1 reference

13 April 2018

Changlian Zhu

15

1 reference

13 April 2018

Qinghe Xing

16

1 reference

13 April 2018

publication date

21 October 2010

1 reference

13 April 2018

Journal of Human Genetics

published in

1 reference

13 April 2018

volume

56

1 reference

13 April 2018

issue

1

1 reference

13 April 2018

page(s)

17-21

1 reference

13 April 2018

Diagnosis, treatment, and prevention of cerebral palsy

cites work

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

The descriptive epidemiology of cerebral palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Prevalence of cerebral palsy in China

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Antenatal risk factors for cerebral palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Estimated frequency of genetic and nongenetic causes of congenital idiopathic cerebral palsy in west Sweden.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Interleukin-6 genotype and risk for cerebral palsy in term and near-term infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Genetic polymorphisms and cerebral palsy in very preterm infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Association of acute ischemic stroke with the MTHFR C677T polymorphism but not with NOS3 gene polymorphisms in a Singapore population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Methylenetetrahydrofolate reductase gene polymorphisms are associated with ischemic and hemorrhagic stroke: Dual effect of MTHFR polymorphisms C677T and A1298C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Thrombophilia: a mechanism of disease in women with adverse pregnancy outcome and thrombotic lesions in the placenta

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Is thrombophilia a factor in the development of hemiplegic cerebral palsy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

An analysis of methylenetetrahydrofolate reductase and glutathione S-transferase omega-1 genes as modifiers of the cerebral response to ischemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Erythropoietin improved neurologic outcomes in newborns with hypoxic-ischemic encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Genetics considerations in cerebral palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

The genomic basis of cerebral palsy: a HuGE systematic literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Role of thrombophilic risk factors in children with non-stroke cerebral palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Cerebral palsy in Norway: prevalence, subtypes and severity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Homocysteine and related genetic polymorphisms in Down's syndrome IQ.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Infant C677T MTHFR polymorphism and severe mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Sex and the pathogenesis of cerebral palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

Different apoptotic mechanisms are activated in male and female brains after neonatal hypoxia-ischaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

7 January 2021

Study of gene expression profiles and biological mechanism of cerebral palsy using a monozygotic twin pair

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

7 January 2021

Candidate Genes and Cerebral Palsy: A Population-Based Study

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

7 January 2021

Genetic polymorphisms and spontaneous preterm birth

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.127

7 January 2021

Identifiers

DOI

10.1038/JHG.2010.127

1 reference

13 April 2018

1 reference

13 April 2018