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A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease
(Blackwell Science, 1999-05-01)
We assessed the effect of a recently described mutation in the MTHFR gene (1298 A --> C) on the risk of deep venous thrombosis (DVT) by determining its prevalence in 190 patients with verified DVT and in age-, race- and ...
A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease
(Blackwell Science, 1999-05-01)
We assessed the effect of a recently described mutation in the MTHFR gene (1298 A --> C) on the risk of deep venous thrombosis (DVT) by determining its prevalence in 190 patients with verified DVT and in age-, race- and ...
Frequency of 677C -> T and 1298A -> C polymorphisms in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene in Turner syndrome individuals
(Sociedade Brasileira de Genética, 2006)
Pollymorphisms in the CBS Gene and Homocysteine, Folate and Vitamin B(12) Levels: Association With Polymorphisms in the MTHFR and MTRR Genes in Brazilian Children
(WILEY-LISS, 2008)
Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR), methionine synthase reductase (MTRR) and cystathionine P-synthase (CBS) genes, involved in the intracellular metabolism of homocysteine (Hcy), can result ...
Polymorphisms of methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), and thymidylate synthase (TYMS) in multiple myeloma risk
(Pergamon-elsevier Science LtdOxfordInglaterra, 2008)
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil
(BIOMED CENTRAL LTD, 2011)
Background/Aim: Hyperhomocysteinemia due to Methylenetetrahydrofolate Reductase (MTHFR) gene, in particular the C677T (Ala222Val) polymorphism were recently associated to steatosis and fibrosis. We analyzed the frequency ...
Genotipagem do polimorfismo A1298C do gene MTHFR em pacientes do HEMOAP diagnosticados com anemia ferropriva
(UNIFAP - Universidade Federal do AmapáBrasil, 11-06-2018)
Introduction: Anemia, characterized by low concentration of hemoglobin levels, is caused by several factors. Iron deficiency anemia is the most common and especially affects children and adolescents, women of childbearing ...
The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease
(Associação Brasileira de Divulgação Científica, 2006-10-01)
Sickle cell disease (SCD) is one of the most common inherited diseases in the world and the patients present notorious clinical heterogeneity. It is known that patients with SCD present activation of the blood coagulation ...