Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with inflammatory bowel disease, and its clinical implications
Mahmud N, Molloy A, McPartlin J, et al. Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with inflammatory bowel disease, and its clinical implications. Gut 1999;45:389-94.
Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with IBD
Nielsen JN, Larsen TB, Fredholm L, et al. Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with IBD. Gut 2000;47:456-7.
Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis
Vecchi M, Sacchi E, Saibeni S, et al. Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis. Dig Dis Sci 2000;45:1465-9.
Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease
Papa A, De Stefano V, Danese S, et al. Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease: Am J Gastroenterol 2001;96:2677-82.
Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease
Guedon C, Le Cam-Duchez, Lalaude O, et al. Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease. Am J Gatroenterol 2001;96:1448-54.
Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: Relation to transcobolamin and homocysteine concentration in blood
Namour F, Olivier JL, Abdelmouttaleb I, et al. Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobolamin and homocysteine concentration in blood. Blood 2001;97:1092-8.
High prevalence of hyperhomocysteinemia related to folate deficiency and mutated 677 C→MTHFR, in the coast of West Africa
Amouzou E, Chabi N, Adjalla C, et al. High prevalence of hyperhomocysteinemia related to folate deficiency and mutated 677 C→MTHFR, in the coast of West Africa. Am J Clin Nutr 2004;79:619-24.
Genetic determinants of folates and vitamin B12 metabolisms: A common pathway in neural tube defect and Down syndrome
Guéant JL, Rodriguez-Guéant RM, Anello G, et al. Genetic determinants of folates and vitamin B12 metabolisms: a common pathway in neural tube defect and Down syndrome. Clin Chem Lab Med 2003;41:1473-7.