Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Ana M. Bea"'
Autor:
Victoria Marco-Benedí, Ana M. Bea, Ana Cenarro, Estíbaliz Jarauta, Martín Laclaustra, Fernando Civeira
Publikováno v:
Lipids in Health and Disease, Vol 21, Iss 1, Pp 1-9 (2022)
Abstract Background Familial hypercholesterolemia (FH) is a codominant autosomal disease characterized by high low-density lipoprotein cholesterol (LDLc) and a high risk of premature cardiovascular disease (CVD). The molecular bases have been well de
Externí odkaz:
https://doaj.org/article/d895cb040eaa42aa834a09f4b5eb070e
Autor:
Lucía Baila-Rueda, Itziar Lamiquiz-Moneo, Estíbaliz Jarauta, Rocío Mateo-Gallego, Sofía Perez-Calahorra, Victoria Marco-Benedí, Ana M. Bea, Ana Cenarro, Fernando Civeira
Publikováno v:
Journal of Translational Medicine, Vol 16, Iss 1, Pp 1-9 (2018)
Abstract Background Familial hypercholesterolemia (FH) is a genetic disorder that result in abnormally high low-density lipoprotein cholesterol levels, markedly increased risk of coronary heart disease (CHD) and tendon xanthomas (TX). However, the cl
Externí odkaz:
https://doaj.org/article/07a7ade516274cedb4478a33dc025869
Autor:
Itziar Lamiquiz-Moneo, Ana M. Bea, Cristian Palacios-Pérez, Pilar De Miguel-Etayo, Esther M. González-Gil, Chuan López-Ariño, Fernando Civeira, Luis A. Moreno, Rocio Mateo-Gallego
Publikováno v:
Cells, Vol 9, Iss 3, p 693 (2020)
Introduction: The global prevalence of type 2 diabetes (T2D) is increasing rapidly, especially in low- and middle-income countries and has a high number of associated comorbidities. Plasmatic concentrations of branched chain amino acids (BCAA) and re
Externí odkaz:
https://doaj.org/article/f538004fd02d4b2182df08296e7a05f4
Autor:
Ana M. Bea, Asier Larrea-Sebal, Victoria Marco-Benedi, Kepa B. Uribe, Unai Galicia-Garcia, Itziar Lamiquiz-Moneo, Martín Laclaustra, Belén Moreno-Franco, Pablo Fernandez-Corredoira, Salvador Olmos, Fernando Civeira, César Martin, Ana Cenarro
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 43:1066-1077
Background: apo (apolipoprotein) E has crucial role in lipid metabolism. The genetic variation in APOE gene is associated with monogenic disorders and contributes to polygenic hypercholesterolemia and to interindividual variability in cholesterol. AP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fafe9809b17ed74703e54072d1617dfc
https://doi.org/10.1161/atvbaha.123.318977
https://doi.org/10.1161/atvbaha.123.318977
Autor:
Ana M Bea, Ana Cenarro, Victoria Marco-Bened, Martn Laclaustra, Csar Martn, Daiana Ibarretxe, Xavier Pint, Teresa Arrobas, Clara Vials, Fernando Civeira, Salvador Olmos
Publikováno v:
Clinical Chemistry. 69:140-148
Background Familial dysbetalipoproteinemia (FDBL) is a monogenic disease due to variants in APOE with a highly variable phenotype. Current diagnostic lipid-based methods have important limitations. The objective is twofold: to define characteristics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0d7644d452279d3d27d5dfc2e0ff7f4
https://doi.org/10.1093/clinchem/hvac213
https://doi.org/10.1093/clinchem/hvac213
Autor:
Victoria Marco-Benedí, Ana M. Bea, Rosa M. Sánchez Hernández, Núria Plana, Pedro Valdivielso, Fernando Civeira
Publikováno v:
Clínica e Investigación en Arteriosclerosis. 34:303-310
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db09a898b9c4a2038e81ce020697ec4f
https://doi.org/10.1016/j.arteri.2022.03.007
https://doi.org/10.1016/j.arteri.2022.03.007
Autor:
Rocío Mateo-Gallego, Sofía Pérez-Calahorra, Ana M. Bea, Irene Gracia-Rubio, Carmen Rodrigo-Carbo, Belen Moreno-Franco, Fernando Civeira, Martín Laclaustra, Itziar Lamiquiz-Moneo
Publikováno v:
Clínica e Investigación en Arteriosclerosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9abf77891e77c765cbaedee84c9b2fe8
https://doi.org/10.1016/j.arteri.2023.04.003
https://doi.org/10.1016/j.arteri.2023.04.003
Akademický článek
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Publikováno v:
Clínica e Investigación en Arteriosclerosis. 33:50-55
Dysbetalipoproteinaemia (or type III hyperlipoproteinaemia) is a severe mixed hyperlipidaemia resulting from the accumulation of remnant chylomicron and VLDL particles in plasma, also called β-VLDL. It is caused by a defect in the recognition by hep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a675648c691d36e2fd727d278b5eeb2
https://doi.org/10.1016/j.arteri.2021.01.002
https://doi.org/10.1016/j.arteri.2021.01.002
Autor:
Núria Plana, Ana M. Bea, Martín Laclaustra, Ángel Brea, Rosa M. Sánchez-Hernández, Victoria Marco-Benedí, Manuel Suárez-Tembra, Fernando Civeira, Xavier Pintó
Publikováno v:
Atherosclerosis. 320:47-52
Background and aims Familial hypercholesterolemia (FH) is a codominant autosomal disease characterized by a high risk of cardiovascular disease when not in lipid-lowering treatment. However, there is a large variability in the clinical presentation i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62f5054b806c2e0e8e4cb893ee0a831d
https://doi.org/10.1016/j.atherosclerosis.2021.01.015
https://doi.org/10.1016/j.atherosclerosis.2021.01.015