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The Glu298Asp variant of the endothelial nitric oxide synthase gene is associated with an increased risk for abruptio placentae in pre-eclampsia

Journal of human genetics, 2005-09, Vol.50 (8), p.415-419

2005

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Altered plasma neurokinin B levels in patients with pre-eclampsia

Archives of gynecology and obstetrics, 2007-08, Vol.276 (2), p.151-157

2007

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Prediction of Preeclampsia – A Workshop Report

Placenta, 2008-03, Vol.29 (Suppl A), p.83-85

2008

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Parallel assessment of circulatory fetal DNA and corticotropin-releasing hormone mRNA in early- and late-onset preeclampsia

Clinical chemistry (Baltimore, Md.), 2005-09, Vol.51 (9), p.1730-1733

2005

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Analysis of plasma elastase levels in early and late onset preeclampsia

Archives of gynecology and obstetrics, 2006-01, Vol.273 (4), p.239-242

2006

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Altered circulating neurokinin B (NKB) levels are not due to sequence variants in the encoding genes

European journal of obstetrics & gynecology and reproductive biology, 2008-09, Vol.140 (1), p.135-136

2008

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Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria

Human molecular genetics, 1999-08, Vol.8 (8), p.1517-1522

1999

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Circulatory nucleosome levels are significantly increased in early and late-onset preeclampsia

Prenatal diagnosis, 2005-08, Vol.25 (8), p.700-703

2005

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Third trimester plasma neurokinin B levels in women with and without preeclampsia

The journal of maternal-fetal & neonatal medicine, 2008-01, Vol.21 (2), p.95-100

2008

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Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction

European journal of obstetrics & gynecology and reproductive biology, 2001-08, Vol.97 (2), p.174-177

2001

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Minimal Alteration in the Ratio of Circulatory Fetal DNA to Fetal Corticotropin-Releasing Hormone mRNA Level in Preeclampsia

Fetal diagnosis and therapy, 2006-01, Vol.21 (3), p.246-249

2006

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Mutations in prothrombin and factor V genes do not contribute significantly to placental vasculopathy in a high-risk patient cohort in South Africa

South African medical journal, 2002-07, Vol.92 (7), p.526-527

2002

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Lipoprotein(A) determination and risk of cardiovascular disease in South African patients with familial hypercholesterolaemia

South African medical journal, 2000-04, Vol.90 (4), p.374-378

2000

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Multiple sclerosis, porphyria-like symptoms, and a history of iron deficiency anemia in a family of Scottish descent

American journal of medical genetics, 1999-09, Vol.86 (2), p.194-196

1999

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The Glu298Asp variant of the endothelial nitric oxide synthase gene is associated with an increased risk for abruptio placentae in pre-eclampsia

Altered plasma neurokinin B levels in patients with pre-eclampsia

Prediction of Preeclampsia – A Workshop Report

Parallel assessment of circulatory fetal DNA and corticotropin-releasing hormone mRNA in early- and late-onset preeclampsia

Analysis of plasma elastase levels in early and late onset preeclampsia

Altered circulating neurokinin B (NKB) levels are not due to sequence variants in the encoding genes

Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria

Circulatory nucleosome levels are significantly increased in early and late-onset preeclampsia

Third trimester plasma neurokinin B levels in women with and without preeclampsia

Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction

Minimal Alteration in the Ratio of Circulatory Fetal DNA to Fetal Corticotropin-Releasing Hormone mRNA Level in Preeclampsia

Mutations in prothrombin and factor V genes do not contribute significantly to placental vasculopathy in a high-risk patient cohort in South Africa

Lipoprotein(A) determination and risk of cardiovascular disease in South African patients with familial hypercholesterolaemia

Multiple sclerosis, porphyria-like symptoms, and a history of iron deficiency anemia in a family of Scottish descent

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