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Comparison of genetic versus clinical diagnosis in familial hypercholesterolemia.
Civeira F, Ros E, Jarauta E, Plana N, Zambon D, Puzo J, Martinez de Esteban JP, Ferrando J, Zabala S, Almagro F, Gimeno JA, Masana L, Pocovi M. Civeira F, et al. Among authors: pocovi m. Am J Cardiol. 2008 Nov 1;102(9):1187-93, 1193.e1. doi: 10.1016/j.amjcard.2008.06.056. Epub 2008 Aug 27. Am J Cardiol. 2008. PMID: 18940289
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. Among authors: pocovi m. Atherosclerosis. 2012 Jun;222(2):449-55. doi: 10.1016/j.atherosclerosis.2012.03.011. Epub 2012 Mar 16. Atherosclerosis. 2012. PMID: 22481068
[Differences in clinical presentation between subjects with a phenotype of familial hypercholesterolemia determined by defects in the LDL-receptor and defects in Apo B-100].
García-Alvarez I, Castillo S, Mozas P, Tejedor D, Reyes G, Artieda M, Cenarro A, Alonso R, Mata P, Pocovi M, Civeira F; Grupo de Estudio de la Hipercolesterolemia Familiar. García-Alvarez I, et al. Among authors: pocovi m. Rev Esp Cardiol. 2003 Aug;56(8):769-74. doi: 10.1016/s0300-8932(03)76955-3. Rev Esp Cardiol. 2003. PMID: 12892621 Free article. Spanish.
168 results