Associated Papers
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Pediatric Nephrology (berlin, Germany), 2016
Common genetic risk factors of venous thromboembolism in Western and Asian populations.
Huang SS et al.
Genetics and Molecular Research : Gmr, 2016
Hyperhomocysteinemia and hypercoagulability in primary biliary cirrhosis.
Biagini MR et al.
World Journal of Gastroenterology, 2006
Clinical applications of bioinformatics, genomics, and pharmacogenomics.
Iqbal O et al.
Methods in Molecular Biology (clifton, N.j.), 2006
Homocysteine is a risk factor for cerebral small vessel disease, acting via endothelial dysfunction.
Hassan A et al.
Brain : a Journal of Neurology, 2004
Absence of Factor V Leiden, thrombomodulin and prothrombin gene variants in Black South African women with pre-eclampsia and eclampsia.
Hira B et al.
Bjog : an International Journal of Obstetrics and Gynaecology, 2003
Genetic susceptibility to venous thrombosis.
Seligsohn U et al.
The New England Journal of Medicine, 2001
Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition.
Chen Z et al.
Human Molecular Genetics, 2001
High prevalence of mild hyperhomocysteinemia in patients with abdominal aortic aneurysm.
Brunelli T et al.
Journal of Vascular Surgery, 2000
Nephrotic-Range Proteinuria and Peripheral Edema in a Child: Not Only Idiopathic Nephrotic Syndrome.
Dolcemascolo V et al.
Case Reports in Nephrology and Dialysis, 0
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