(Q54569451)

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High frequency of methylenetetrahydrofolate reductase 677TT genotype in Hungarian HELLP syndrome patients determined by quantitative real-time PCR.

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

High frequency of methylenetetrahydrofolate reductase 677TT genotype in Hungarian HELLP syndrome patients determined by quantitative real-time PCR. (English)

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

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author name string

Nagy B

1

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

Hupuczi P

2

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

Papp Z

3

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

publication date

30 November 2006

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

Journal of Human Hypertension

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

21

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

2

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

154-158

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Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

Thrombophilia and pregnancy

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Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia.

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Maternal and neonatal outcome of preeclamptic pregnancies: the potential roles of factor V Leiden mutation and 5,10 methylenetetrahydrofolate reductase

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Hyperhomocysteinaemia: a risk factor for preeclampsia?

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Etiology and pathogenesis of preeclampsia: current concepts

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A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis

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Hyperhomocysteinemia: a risk factor for placental abruption or infarction.

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Thrombosis in pregnancy: maternal and fetal issues

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The DNA isolation method has effect on allele drop-out and on the results of fluorescent PCR and DNA fragment analysis.

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Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia.

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Frequency of factor V, prothrombin and methylenetetrahydrofolate reductase gene variants in preeclampsia

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Methylenetetrahydrofolate reductase polymorphism and pre-eclampsia

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Adverse pregnancy outcomes are associated with multiple maternal thrombophilic factors.

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Searching for preeclampsia genes: the current position.

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Dyslipidemia, iron, and oxidative stress in preeclampsia: assessment of maternal and feto-placental interactions

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Prothrombin 20210 G-->A, MTHFR C677T mutations in women with venous thromboembolism associated with pregnancy

1 reference

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7 January 2021

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Factor V Leiden and thermolabile methylenetetrahydrofolate reductase gene variants in an East Anglian preeclampsia cohort

1 reference

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7 January 2021

based on heuristic

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Genetic susceptibility to preeclampsia: roles of cytosineto-thymine substitution at nucleotide 677 of the gene for methylenetetrahydrofolate reductase, 68-base pair insertion at nucleotide 844 of the gene for cystathionine beta-synthase, and factor

1 reference

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7 January 2021

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Identifiers

10.1038/SJ.JHH.1002122

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17136107

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