rs137852769
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Neither maternal nor fetal heterozygosity for the E474Q mutation is a relevant factor of HELLP syndrome.
|
17313315 |
2007 |
rs137852769
|
|
|
0.020 |
GeneticVariation |
BEFREE |
While carrying fetuses with the Glu474Gln mutation, 79 percent of the heterozygous mothers had fatty liver of pregnancy or the HELLP syndrome.
|
10352164 |
1999 |
rs1137100
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However the LEPR c.326A>G AG genotype was twice more frequent and the (AG AG GG AG) haplotype was three times more frequent in HELLP syndrome patients.
|
20149225 |
2010 |
rs56149945
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The BclI, N363S, and ER22/23EK polymorphisms of the GR gene were determined in 300 healthy pregnant women, 150 pregnant women with severe preeclampsia including 17 pregnant women with HELLP syndrome.
|
19336230 |
2009 |
rs1188383936
|
|
|
0.010 |
GeneticVariation |
BEFREE |
As hemolysis, elevated liver enzymes, low platelets (HELLP) syndrome is one of the most severe forms of pre-eclampsia we aimed to assess the prevalence of the factor V Leiden, the prothrombin 20210G >A mutation and the methylenetetrahydrofolate reductase (MTHFR) 677C >T polymorphism in women with HELLP syndrome and in their fetuses from the same index pregnancy.
|
18568463 |
2008 |
rs1217691063
|
|
|
0.010 |
GeneticVariation |
BEFREE |
As hemolysis, elevated liver enzymes, low platelets (HELLP) syndrome is one of the most severe forms of pre-eclampsia we aimed to assess the prevalence of the factor V Leiden, the prothrombin 20210G >A mutation and the methylenetetrahydrofolate reductase (MTHFR) 677C >T polymorphism in women with HELLP syndrome and in their fetuses from the same index pregnancy.
|
18568463 |
2008 |
rs4986790
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We determined five common mutations in TLR4 (D299G and T399I) and NOD2 (R702W, G908R and L1007fs) in 340 primiparous women with a history of early-onset preeclampsia, of whom 177 women developed HELLP syndrome and in 113 women with a history of only uneventful pregnancies as controls.
|
18382655 |
2008 |
rs4986791
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We determined five common mutations in TLR4 (D299G and T399I) and NOD2 (R702W, G908R and L1007fs) in 340 primiparous women with a history of early-onset preeclampsia, of whom 177 women developed HELLP syndrome and in 113 women with a history of only uneventful pregnancies as controls.
|
18382655 |
2008 |
rs771184127
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We determined five common mutations in TLR4 (D299G and T399I) and NOD2 (R702W, G908R and L1007fs) in 340 primiparous women with a history of early-onset preeclampsia, of whom 177 women developed HELLP syndrome and in 113 women with a history of only uneventful pregnancies as controls.
|
18382655 |
2008 |
rs268
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Between a small group of patients with nulliparous HELLP syndrome (a variant of severe preeclampsia: hemolysis, elevated liver enzyme, low platelets) patients (n=12) and control subjects, there was a significant difference in the prevalence of the Asn291Ser mutation (16.7% versus 3.0%, P=0.01).
|
11711487 |
2001 |
rs6025
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We report on two patients with HELLP syndrome who were found to be heterozygous for factor V R506Q mutation, leading to activated protein C resistance.
|
8616100 |
1996 |