Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Luis Galdos Alcelay"'
Autor:
Valentina Fernández del Pozo, Fernando Gómez Busto, Maite Álvarez Álvarez, Marian M. de Pancorbo, Miguel A. Alfonso-Sánchez, José A. Peña, Juan José Zarranz Imirizaldu, Luis Galdos Alcelay, Manuel Fernández Martínez
Publikováno v:
Dementia and Geriatric Cognitive Disorders. 21:81-87
Background: Late-onset Alzheimer’s disease (LOAD) is associated with changes in certain proteins, such as ApoE and Cyp46A1, of the elimination route for cerebral cholesterol. The main lipoprotein involved in its transport is ApoE whose υ4 allele i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9fdd173c2bdcae87dc0bc2b51c162b0
https://doi.org/10.1159/000090215
https://doi.org/10.1159/000090215
Autor:
Jessica Castro Flores, Sandra Inglés Borda, Manuel Fernández Martínez, M.C. González-Fernández, María Carrasco Zabaleta, Miryam Barandiarán Amillano, María Ángeles Gómez Beldarraín, Josefa Moraza López, Marian M. de Pancorbo, Xabier Elcoroaristizabal Martín, Begoña Indakoetxea Juanbeltz, Rocio Bereincua Gandarias, Ana Molano Salazar, Nuria Ortiz Marqués, Luis Galdos Alcelay, Juan María Uterga Valiente
Publikováno v:
BMC Neuroscience
Addi. Archivo Digital para la Docencia y la Investigación
instname
BMC Neuroscience, Vol 10, Iss 1, p 125 (2009)
Addi. Archivo Digital para la Docencia y la Investigación
instname
BMC Neuroscience, Vol 10, Iss 1, p 125 (2009)
Background: The aim of this study is to examine the influence of the catechol-O-methyltranferase (COMT) gene (polymorphism Val158 Met) as a risk factor for Alzheimer's disease (AD) and mild cognitive impairment of amnesic type (MCI), and its synergis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b98f405cdc372edb37acdbf9f375f65c
https://doi.org/10.1186/1471-2202-10-125
https://doi.org/10.1186/1471-2202-10-125
Autor:
Xabier Elcoroaristizabal Martín, Sandra Inglés Borda, Iratxe Ugarriza Serrano, Begoña Indakoetxea Juanbeltz, Luis Galdos Alcelay, Juan María Uterga Valiente, Elisa Blanco Martín, Fernando Gómez Busto, Maite Alvarez-Alvarez, Myriam Barandiarán Amillano, Josefa Moraza López, Rocio Bereincua Gandarias, Manuel Fernández-Martínez, María Ángeles Gómez Beldarraín, Marian M. de Pancorbo, Ana Molano Salazar
Publikováno v:
BMJ Open
Objectives: Examine the role of single nucleotide polymorphisms (SNPs) in the oestrogen receptor (ER) genes: rs9340799, rs2234693, rs2228480 (in the ESR1 gene) and rs4986938 (in the ESR2 gene) as a risk factor for amnesic mild cognitive impairment (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca4f4698d8212e02d192a5b3d080f4f4
https://doi.org/10.1136/bmjopen-2013-003200
https://doi.org/10.1136/bmjopen-2013-003200