Listar por autor "Erro Aguirre, María Elena"
Mostrando ítems 1-5 de 5
-
Association of blood-based DNA methylation markers with late-onset alzheimer disease: a potential diagnostic approach
Acha Santamaría, Blanca ; Corroza, Jon; Sánchez Ruiz de Gordoa, Javier ; Cabello, Carolina; Robles Solano, Maitane; Méndez López, Iván ; Macías, Mónica; Zueco, Sara; Roldán, Miren; Urdánoz Casado, Amaya ; Jericó Pascual, Ivonne; Erro Aguirre, María Elena; Alcolea, Daniel; Lleo, Alberto; Blanco Luquin, Idoia; Mendióroz Iriarte, Maite (Lippincott Williams & WilkinsAmerican Academy of Neurology, 2023) Artículo / ArtikuluaBackground and Objectives: There is an urgent need to identify novel noninvasive biomarkers for Alzheimer disease (AD) diagnosis. Recent advances in blood-based measurements of phosphorylated tau (pTau) species are promising ... -
Familial globular glial tauopathy linked to MAPT mutations: molecular neuropathology and seeding capacity of a prototypical mixed neuronal and glial tauopathy
Ferrer, Isidro; Andrés Benito, Pol; Zelaya Huerta, María Victoria ; Erro Aguirre, María Elena; Carmona, Margarita; Ausín, Karina; Lachén Montes, Mercedes ; Fernández Irigoyen, Joaquín ; Santamaría, Enrique; Río, José Antonio del (Springer, 2020) Artículo / ArtikuluaGlobular glial tauopathy (GGT) is a progressive neurodegenerative disease involving the grey matter and white matter (WM) and characterized by neuronal deposition of hyper-phosphorylated, abnormally conformed, truncated, ... -
Is the phenotype designation by PSP-MDS criteria stable throughout the disease course and consistent with tau distribution?
Sánchez Ruiz de Gordoa, Javier ; Zelaya Huerta, María Victoria ; Tellechea-Aramburo, Paula; Acha Santamaría, Blanca ; Roldán, Miren; López Molina, Carlos ; Coca, Valle; Galbete Jiménez, Arkaitz ; Mendióroz Iriarte, Maite; Erro Aguirre, María Elena (Frontiers Media, 2022) Artículo / ArtikuluaIntroduction: the MDS-PSP criteria have shown high sensitivity for the PSP diagnosis, but do not discriminate the phenotype diversity. Our purpose was to search for anatomopathological differences among PSP phenotypes ... -
Liquid biopsy in alzheimer's disease patients reveals epigenetic changes in the PRLHR gene
Macías, Mónica; Acha Santamaría, Blanca ; Corroza, Jon; Urdánoz Casado, Amaya ; Roldán, Miren; Robles, Maitane; Sánchez Ruiz de Gordoa, Javier ; Erro Aguirre, María Elena; Jericó Pascual, Ivonne; Blanco Luquin, Idoia; Mendióroz Iriarte, Maite (MDPI, 2023) Artículo / ArtikuluaIn recent years, new DNA methylation variants have been reported in genes biologically relevant to Alzheimer’s disease (AD) in human brain tissue. However, this AD-specific epigenetic information remains brain-locked and ... -
Parálisis supranuclear progresiva: correlación clínico-patológica y aproximación al papel patogénico de lamicroglía
La parálisis supranuclear progresiva (PSP) es una enfermedad neurodegenerativa que se manifiesta clínicamente como un parkinsonismo atípico y su base patológica son los depósitos de proteína tau en neuronas y células ...