Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Cardiovascular Diseases and HFE[original query] |
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| Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseases. European journal of clinical investigation 2001 May 31 (5): 382-8. Hetet G, Elbaz A, Gariepy J, Nicaud V, Arveiler D, Morrison C, Kee F, Evans A, Simon A, Amarenco P, Cambien F, Grandchamp |
| Association between HFE mutations and acute myocardial infarction: a study in patients from Northern and Southern Italy. Blood cells, molecules & diseases 0 31 (1): 57-62. Candore Giuseppina, Balistreri Carmela Rita, Lio Domenico, Mantovani Vilma, Colonna-Romano Giuseppina, Chiappelli Martina, Tampieri Cecilia, Licastro Federico, Branzi Angelo, Averna Maurizio, Caruso Marco, Hoffmann Enrico, Caruso Caloge |
| Highly sensitivity adhesion molecules detection in hereditary haemochromatosis patients reveals altered expression. International journal of immunogenetics 2010 Apr 37 (2): 125-33. Norris S, White M, Mankan A K, Lawless M |
| MTHFR and HFE, but not preproghrelin and LBP, polymorphisms as risk factors for all-cause end-stage renal disease development. Folia biologica 2014 60 (2): 83-8. Bloudí?ková S, Kuthanová L, Hubá?ek J A, |
| Correlation between HFE gene polymorphisms and increased risk of coronary artery disease among patients with type 2 diabetes in Iran. Turkish journal of medical sciences 2016 46 (3): 590-6. Saremi Leila, Saremi Marzieh, Lotfipanah Shirin, ?mani Saber, Fu Junjiang, Zhang Tian |
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