Zobrazeno 1 - 10
of 27
pro vyhledávání: '"María Elena Erro"'
Autor:
Mónica Macías, Blanca Acha, Jon Corroza, Amaya Urdánoz-Casado, Miren Roldan, Maitane Robles, Javier Sánchez-Ruiz de Gordoa, María Elena Erro, Ivonne Jericó, Idoia Blanco-Luquin, Maite Mendioroz
Publikováno v:
Cells, Vol 12, Iss 23, p 2679 (2023)
In 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 unreachable during patients
Externí odkaz:
https://doaj.org/article/b7d9ab9b172f4a2f8f2be99d0b7e8b4a
Autor:
Idoia Blanco-Luquin, Miren Altuna, Javier Sánchez-Ruiz de Gordoa, Amaya Urdánoz-Casado, Miren Roldán, María Cámara, Victoria Zelaya, María Elena Erro, Carmen Echavarri, Maite Mendioroz
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-10 (2018)
Abstract Background Whole-exome sequencing has revealed a rare missense variant in PLD3 gene (rs145999145) to be associated with late onset Alzheimer’s disease (AD). Nevertheless, the association remains controversial and little is known about the
Externí odkaz:
https://doaj.org/article/6fbd856a73dc4f0a8df9185e96edf61b
Autor:
Fernández, Alejandra Collía, Horga, Alejandro, Prieto, Ana Barragán, del Villar Igea, Ana, Núñez, Ana Urbanos, Serrano, Ángel Aledo, García, Araceli, Menéndez, Beatriz Martínez, Recasens, Bernat Bertran, Serrano, Blanca Serrano, de la Esperanza, Blanca Talavera, de la Hoz, Carlos Pablo de Fuenmayor Fernández, Juste, Carlos Tejero, Martín, Carmen Valderrama, García, Cristina Fernández, Ochoa, Marta, Íñiguez, Cristina, García, Daniel Macías, Pérez Martínez, David A., Santacruz, Débora Mª. Cerdán, Robert, Misericòrdia Floriach, Gomez, Elisabet Franquet, Puiggròs, Elsa, Álvarez, Eric Freire, Llamas, Esteban Peña, Villareal, Estibaliz, Díaz, Eva Fernández, Burguillos, Fernando Morejón, Beitia, Garazi Agirre, Gutiérrez-Gutiérrez, Gerardo, Monteiro, Guilherme Carvalho, Ygual, Guillermo Cervera, Hernández, Guillermo, Rubio, Guillermo, Alonso, Hortenia, Froiz, Iago Payo, García, Iago Rego, Peñas, Inmaculada Redondo, Pérez Sánchez, Javier R., García, Javier Tejada, Álvarez, Javier Villacieros, Domínguez, Jéssica Fernández, Etessam, Jesús Porta, Equiza, Jon, Pascual, Jorge Millán, Usieto, José Antonio Oliván, Reyes, José Antonio, Gómez, José Balseiro, Bueno, José Carlos Roche, Velasquez, Jose Luis Camacho, López, José María Barrios, Raquel Lamas, Leire Ainz, Lezama, Lidia Binela Lara, Caballero, Lorena, Davila, Lucía Galan, González, Nuria, de Antonio, Luis Alberto Rodríguez, Torres, Mª. Araceli García, Zabaleta, Maite Martinez, Rodríguez, Manuel Medina, Moragues, María Dolores, García, María Fuensanta Valero, Hernández, María, Abildúa, María José Abenza, Rabasa, María, Santos, María Rico, Usero, María, Zurdo, Martín, Más, Miguel, Maneiro, Miren, Platas, Montserrat González, Muriana, Nafría, Noelia González, Esteve, Oriol Barrachina, del Saz Saucedo, Pablo, Rocío, Vilar Ventura, Rosa M., Atienza, Saida, Navas, Sandra Rodríguez, Fernández, Santiago Fernández, Borja, Sergio, Navarro, Silvia Gil, García, Solange Kapetanovic, García, Susana, Salas, Teresa Mateos, Palasí, Toni, Cantero, Victoriano Romero, García-Azorín, David, Aguirre, María Elena Erro, Moncó, Juan Carlos García, Guijarro-Castro, Cristina, Delgado, Fernando Romero, Andrés, José Miguel Láinez, Ezpeleta, David
Publikováno v:
In Journal of the Neurological Sciences 15 April 2021 423
Autor:
Blanca Acha, Jon Corroza, Javier Sánchez-Ruiz de Gordoa, Sara Zueco, Maitane Robles, Iván Méndez-López, Mónica Macías Conde, Carolina Cabello, Miren Roldan, Amaya Urdánoz-Casado, Ivonne Jericó, María Elena Erro, Daniel Alcolea, Alberto LLeó, Idoia Blanco-Luquin, Maite Mendioroz
Background: This work investigated the diagnostic accuracy of a blood-based DNA methylation marker panel as a non-invasive tool to identify Alzheimer's disease (AD) patients. Methods: Blood DNA methylation levels at 46 CpG sites (21 genes selected af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49f644fff0b7b50a15900af386136891
https://doi.org/10.21203/rs.3.rs-2385191/v1
https://doi.org/10.21203/rs.3.rs-2385191/v1
Autor:
Amaya Urdánoz-Casado, Maite Mendioroz, Javier Sánchez-Ruiz de Gordoa, María Victoria Zelaya, Janire Vicuña-Urriza, Miren Roldán, Blanca Acha, Sara Zueco, Idoia Blanco-Luquin, Paula Tellechea, María Elena Erro
Publikováno v:
Movement Disorders. 35:885-890
BACKGROUND The role of the microglia-related gene triggering receptor expressed in myeloid cells 2 (TREM2) in primary tauopathies, such as progressive supranuclear palsy (PSP), still remains unclear. OBJECTIVES The objective of this study was to prof
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9881de25b797a8a2aadcc88ec926089
https://doi.org/10.1002/mds.27992
https://doi.org/10.1002/mds.27992
Autor:
Miren Altuna, Rosa Larumbe, María Victoria Zelaya, Sira Moreno, Virginia García-Solaesa, Maite Mendioroz, María Antonia Ramos, María Elena Erro
Publikováno v:
JOURNAL OF NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Introduction Autosomal dominant Alzheimer's disease (ADAD) due to presenilin 1 (PSEN1) mutation can induce atypical neurological symptoms such as movement disorders and epileptic seizures in the context of early-onset progressive cognitive impairment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3c5220548f57522f138da5c7bfb1139
https://pubmed.ncbi.nlm.nih.gov/35438347
https://pubmed.ncbi.nlm.nih.gov/35438347
Publikováno v:
Revista de Neurología. 75:75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78be499904a8e01e0c408b5eb1d62c34
https://doi.org/10.33588/rn.7503.2021234
https://doi.org/10.33588/rn.7503.2021234
Autor:
María Cámara, María Elena Erro, Victoria Zelaya, Idoia Blanco-Luquin, Miren Altuna, Miren Roldán, Maite Mendioroz, Javier Sánchez-Ruiz de Gordoa, Amaya Urdánoz-Casado, Carmen Echavarri
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-10 (2018)
Clinical Epigenetics
Clinical Epigenetics
Background Whole-exome sequencing has revealed a rare missense variant in PLD3 gene (rs145999145) to be associated with late onset Alzheimer’s disease (AD). Nevertheless, the association remains controversial and little is known about the role of P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfe9d567218b2403c06b0725ef02aae9
http://link.springer.com/article/10.1186/s13148-018-0547-3
http://link.springer.com/article/10.1186/s13148-018-0547-3
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
David García-Azorín, María José Abenza Abildúa, María Elena Erro Aguirre, Santiago Fernández Fernández, Juan Carlos García Moncó, Cristina Guijarro-Castro, Montserrat González Platas, Fernando Romero Delgado, José Miguel Láinez Andrés, David Ezpeleta, Alejandra Collía Fernández, Alejandro Horga, Ana Barragán Prieto, Ana del Villar Igea, Ana Urbanos Núñez, Ángel Aledo Serrano, Araceli García, Beatriz Martínez Menéndez, Bernat Bertran Recasens, Blanca Serrano Serrano, Blanca Talavera de la Esperanza, Carlos Pablo de Fuenmayor Fernández de la Hoz, Carlos Tejero Juste, Carmen Valderrama Martín, Cristina Fernández García, Marta Ochoa, Cristina Íñiguez, Daniel Macías García, David A. Pérez Martínez, Débora Mª. Cerdán Santacruz, Misericòrdia Floriach Robert, Elisabet Franquet Gomez, Elsa Puiggròs, Eric Freire Álvarez, Esteban Peña Llamas, Estibaliz Villareal, Eva Fernández Díaz, Fernando Morejón Burguillos, Garazi Agirre Beitia, Gerardo Gutiérrez-Gutiérrez, Guilherme Carvalho Monteiro, Guillermo Cervera Ygual, Guillermo Hernández, Guillermo Rubio, Hortenia Alonso, Iago Payo Froiz, Iago Rego García, Inmaculada Redondo Peñas, Javier R. Pérez Sánchez, Javier Tejada García, Javier Villacieros Álvarez, Jéssica Fernández Domínguez, Jesús Porta Etessam, Jon Equiza, Jorge Millán Pascual, José Antonio Oliván Usieto, José Antonio Reyes, José Balseiro Gómez, José Carlos Roche Bueno, Jose Luis Camacho Velasquez, José María Barrios López, Leire Ainz Raquel Lamas, Lidia Binela Lara Lezama, Lorena Caballero, Lucía Galan Davila, Nuria González, Luis Alberto Rodríguez de Antonio, Mª. Araceli García Torres, Maite Martinez Zabaleta, Manuel Medina Rodríguez, María Dolores Moragues, María Fuensanta Valero García, María Hernández, María Rabasa, María Rico Santos, María Usero, Martín Zurdo, Miguel Más, Miren Maneiro, null Muriana, Noelia González Nafría, Oriol Barrachina Esteve, Pablo del Saz Saucedo, null Rocío, Rosa M. Vilar Ventura, Saida Atienza, Sandra Rodríguez Navas, Sergio Borja, Silvia Gil Navarro, Solange Kapetanovic García, Susana García, Teresa Mateos Salas, Toni Palasí, Victoriano Romero Cantero
Publikováno v:
Journal of the Neurological Sciences
Objective We report the findings from the Spanish Society of Neurology's NeuroCOVID-19 Registry. Methods We performed a multicentre study of patients with neurological manifestations of COVID-19. Participating physicians reported demographic, clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67f75c0e00e8f52ccd1cf62d3931de39
https://doi.org/10.1016/j.jns.2020.117283
https://doi.org/10.1016/j.jns.2020.117283