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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. 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
The p.Leu167del Mutation in APOE Gene Causes Autosomal Dominant Hypercholesterolemia by Down-regulation of LDL Receptor Expression in Hepatocytes.
Cenarro A, Etxebarria A, de Castro-Orós I, Stef M, Bea AM, Palacios L, Mateo-Gallego R, Benito-Vicente A, Ostolaza H, Tejedor T, Martín C, Civeira F. Cenarro A, et al. Among authors: de castro oros i. J Clin Endocrinol Metab. 2016 May;101(5):2113-21. doi: 10.1210/jc.2015-3874. Epub 2016 Mar 25. J Clin Endocrinol Metab. 2016. PMID: 27014949
Cosegregation of serum cholesterol with cholesterol intestinal absorption markers in families with primary hypercholesterolemia without mutations in LDLR, APOB, PCSK9 and APOE genes.
Baila-Rueda L, Pérez-Ruiz MR, Jarauta E, Tejedor MT, Mateo-Gallego R, Lamiquiz-Moneo I, de Castro-Orós I, Cenarro A, Civeira F. Baila-Rueda L, et al. Atherosclerosis. 2016 Mar;246:202-7. doi: 10.1016/j.atherosclerosis.2016.01.005. Epub 2016 Jan 6. Atherosclerosis. 2016. PMID: 26802983
Apolipoprotein E gene mutations in subjects with mixed hyperlipidemia and a clinical diagnosis of familial combined hyperlipidemia.
Solanas-Barca M, de Castro-Orós I, Mateo-Gallego R, Cofán M, Plana N, Puzo J, Burillo E, Martín-Fuentes P, Ros E, Masana L, Pocoví M, Civeira F, Cenarro A. Solanas-Barca M, et al. Atherosclerosis. 2012 Jun;222(2):449-55. doi: 10.1016/j.atherosclerosis.2012.03.011. Epub 2012 Mar 16. Atherosclerosis. 2012. PMID: 22481068
23 results