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Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study.
Martinelli N, Olivieri O, Shen GQ, Trabetti E, Pizzolo F, Busti F, Friso S, Bassi A, Li L, Hu Y, Pignatti PF, Corrocher R, Wang QK, Girelli D. Martinelli N, et al. Among authors: busti f. BMC Med Genet. 2009 May 13;10:41. doi: 10.1186/1471-2350-10-41. BMC Med Genet. 2009. PMID: 19439088 Free PMC article.
Reduced serum hepcidin levels in patients with chronic hepatitis C.
Girelli D, Pasino M, Goodnough JB, Nemeth E, Guido M, Castagna A, Busti F, Campostrini N, Martinelli N, Vantini I, Corrocher R, Ganz T, Fattovich G. Girelli D, et al. Among authors: busti f. J Hepatol. 2009 Nov;51(5):845-52. doi: 10.1016/j.jhep.2009.06.027. Epub 2009 Aug 12. J Hepatol. 2009. PMID: 19729219 Free PMC article.
DISHphagia: an unusual cause of dysphagia.
Martinelli N, Busti F, Girelli D, Olivieri O. Martinelli N, et al. Among authors: busti f. J Clin Endocrinol Metab. 2012 Aug;97(8):2573-4. doi: 10.1210/jc.2012-1343. Epub 2012 May 8. J Clin Endocrinol Metab. 2012. PMID: 22569242 No abstract available.
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients.
Pelucchi S, Mariani R, Calza S, Fracanzani AL, Modignani GL, Bertola F, Busti F, Trombini P, Fraquelli M, Forni GL, Girelli D, Fargion S, Specchia C, Piperno A. Pelucchi S, et al. Among authors: busti f. Haematologica. 2012 Dec;97(12):1818-25. doi: 10.3324/haematol.2012.062661. Epub 2012 Jul 6. Haematologica. 2012. PMID: 22773607 Free PMC article.
Increased serum hepcidin levels in subjects with the metabolic syndrome: a population study.
Martinelli N, Traglia M, Campostrini N, Biino G, Corbella M, Sala C, Busti F, Masciullo C, Manna D, Previtali S, Castagna A, Pistis G, Olivieri O, Toniolo D, Camaschella C, Girelli D. Martinelli N, et al. Among authors: busti f. PLoS One. 2012;7(10):e48250. doi: 10.1371/journal.pone.0048250. Epub 2012 Oct 29. PLoS One. 2012. PMID: 23144745 Free PMC article.
Paraoxonase-1 status in patients with hereditary hemochromatosis.
Martinelli N, García-Heredia A, Roca H, Aranda N, Arija V, Mackness B, Mackness M, Busti F, Aragonès G, Pedro-Botet J, Pedica F, Cataldo I, Marsillach J, Joven J, Girelli D, Camps J. Martinelli N, et al. Among authors: busti f. J Lipid Res. 2013 May;54(5):1484-92. doi: 10.1194/jlr.P028977. Epub 2013 Mar 6. J Lipid Res. 2013. PMID: 23471031 Free PMC article.
68 results