BackBrowsing by Author "Barandiaran Amillano, Miryam"
Now showing items 1-3 of 3
-
Estudio longitudinal y caracterización cognitiva de portadores de la mutación C.709-1G>A en el gen de la Progranulina
(2016-10-28)La Demencia Frontotemporal (DFT) engloba a un grupo de enfermedades neurodegenerativas clínica y neuropatológicamente heterogéneas, que afectan a los lóbulosfrontales y temporales, y cuyos síntomas principales son alteraciones ... -
The COMT Val158 Met polymorphism as an associated risk factor for Alzheimer disease and mild cognitive impairment in APOE 4 carriers
Fernández Martínez, Manuel; Elcoroaristizabal Martín, Xabier; Galdos Alcelay, Luis; Castro Flores, Jessica; Uterga Valiente, Juan MarÍa; Indakoetxea Juanbeltz, Begoña; Gómez Beldarrain, María Angeles; Moraza López, Josefa; González Fernández, María Carmen; Molano Salazar, Ana; Bereincua Gandarias, Rocío; Inglés Borda, Sandra; Ortiz Marqués, Nuria; Barandiaran Amillano, Miryam; Carrasco Zabaleta, María; Martínez de Pancorbo Gómez, María de los Angeles
(BioMed Central, 2009-09)
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 ... -
The Unexpected Co-Occurrence of GRN and MAPT p.A152T in Basque Families: Clinical and Pathological Characteristics
Moreno Izco, Fermín; Indakoetxea Juanbeltz, Begoña; Barandiaran Amillano, Miryam; Caballero, María Cristina; Gorostidi, Ana; Calafell, Francesc; Gabilondo, Alazne; Tainta, Mikel; Zulaica, Miren; Martí Massó, José Félix; López de Munain Arregui, Adolfo José; Sánchez Juan, Pascual; Lee, Suzee E. (Public Library Science, 2017-06-08)
Background The co-occurrence of the c.709-1G > A GRN mutation and the p.A152T MAPT variant has been identified in 18 Basque families affected by frontotemporal dementia (FTD). We aimed to investigate the influence of ...