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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: tejedor mt. 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
Single Nucleotide Variants Associated With Polygenic Hypercholesterolemia in Families Diagnosed Clinically With Familial Hypercholesterolemia.
Lamiquiz-Moneo I, Pérez-Ruiz MR, Jarauta E, Tejedor MT, Bea AM, Mateo-Gallego R, Pérez-Calahorra S, Baila-Rueda L, Marco-Benedí V, de Castro-Orós I, Cenarro A, Civeira F. Lamiquiz-Moneo I, et al. Among authors: tejedor mt. Rev Esp Cardiol (Engl Ed). 2018 May;71(5):351-356. doi: 10.1016/j.rec.2017.07.010. Epub 2017 Sep 14. Rev Esp Cardiol (Engl Ed). 2018. PMID: 28919240 English, Spanish.
Diagnostic yield of sequencing familial hypercholesterolemia genes in individuals with primary hypercholesterolemia.
Lamiquiz-Moneo I, Civeira F, Mateo-Gallego R, Laclaustra M, Moreno-Franco B, Tejedor MT, Palacios L, Martín C, Cenarro A. Lamiquiz-Moneo I, et al. Among authors: tejedor mt. Rev Esp Cardiol (Engl Ed). 2021 Aug;74(8):664-673. doi: 10.1016/j.rec.2020.06.003. Epub 2020 Jul 11. Rev Esp Cardiol (Engl Ed). 2021. PMID: 32660911 English, Spanish.
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. Among authors: tejedor mt. Atherosclerosis. 2016 Mar;246:202-7. doi: 10.1016/j.atherosclerosis.2016.01.005. Epub 2016 Jan 6. Atherosclerosis. 2016. PMID: 26802983
80 results