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Rare genetic variants with large effect on triglycerides in subjects with a clinical diagnosis of familial vs nonfamilial hypertriglyceridemia.
De Castro-Orós I, Civeira F, Pueyo MJ, Mateo-Gallego R, Bolado-Carrancio A, Lamíquiz-Moneo I, Álvarez-Sala L, Fabiani F, Cofán M, Cenarro A, Rodríguez-Rey JC, Ros E, Pocoví M. De Castro-Orós I, et al. Among authors: pocovi m. J Clin Lipidol. 2016 Jul-Aug;10(4):790-797. doi: 10.1016/j.jacl.2016.02.010. Epub 2016 Feb 23. J Clin Lipidol. 2016. PMID: 27578109
Common genetic variants contribute to primary hypertriglyceridemia without differences between familial combined hyperlipidemia and isolated hypertriglyceridemia.
De Castro-Orós I, Cenarro A, Tejedor MT, Baila-Rueda L, Mateo-Gallego R, Lamiquiz-Moneo I, Pocoví M, Civeira F. De Castro-Orós I, et al. Among authors: pocovi m. Circ Cardiovasc Genet. 2014 Dec;7(6):814-21. doi: 10.1161/CIRCGENETICS.114.000522. Epub 2014 Aug 30. Circ Cardiovasc Genet. 2014. PMID: 25176936
Aragon workers' health study--design and cohort description.
Casasnovas JA, Alcaide V, Civeira F, Guallar E, Ibañez B, Borreguero JJ, Laclaustra M, León M, Peñalvo JL, Ordovás JM, Pocovi M, Sanz G, Fuster V. Casasnovas JA, et al. Among authors: pocovi m. BMC Cardiovasc Disord. 2012 Jun 19;12:45. doi: 10.1186/1471-2261-12-45. BMC Cardiovasc Disord. 2012. PMID: 22712826 Free PMC article.
168 results