Literature DB >> 9396508

Common mutation in the methylenetetrahydrofolate reductase gene offers no support for mild hyperhomocysteinemia being a causal risk factor for cardiovascular disease.

L Brattström.   

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Year:  1997        PMID： 9396508

Source DB:  PubMed          Journal:  Circulation        ISSN： 0009-7322            Impact factor:   29.690


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  5 in total

Review 1.  Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: an overview.

Authors:  R Castro; I Rivera; H J Blom; C Jakobs; I Tavares de Almeida
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

Review 2.  Hyperhomocysteinemia and thrombosis.

Authors:  M Cattaneo
Journal:  Lipids       Date:  2001       Impact factor: 1.880

3.  Homocysteine, folate, vitamin B12 levels, and C677T MTHFR mutation in children with renal failure.

Authors:  Alberto Canepa; Alba Carrea; Gianluca Caridi; Laura Dertenois; Giuseppe Minniti; Roberto Cerone; Silvana Canini; Maria Grazia Calevo; Francesco Perfumo
Journal:  Pediatr Nephrol       Date:  2003-02-21       Impact factor: 3.714

4.  Prevalence of methylenetetrahydrofolate gene (MTHFR) C677T polymorphism among chronic hemodialysis patients and its association with cardiovascular disease: a cross-sectional analysis.

Authors:  Salwa Ibrahim; Ola El Dessokiy
Journal:  Clin Exp Nephrol       Date:  2009-05-26       Impact factor: 2.801

5.  Association between serum homocysteine concentration with coronary artery disease in Iranian patients.

Authors:  Ahmad Mirdamadi; Hamid Farzamnia; Pooyan Varzandeh; Naser Almasi; Mahfar Arasteh
Journal:  ARYA Atheroscler       Date:  2011
  5 in total

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