Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Lidia Sánchez‐Puebla"'
Autor:
Lidia Sánchez-Puebla, Inés López-Cuenca, Elena Salobrar-García, María González-Jiménez, Alberto Arias-Vázquez, José A. Matamoros, Ana I. Ramírez, José A. Fernández-Albarral, Lorena Elvira-Hurtado, Takaomi C. Saido, Takashi Saito, Carmen Nieto-Vaquero, María I. Cuartero, María A. Moro, Juan J. Salazar, Rosa de Hoz, José M. Ramírez
Publikováno v:
Biomolecules, Vol 14, Iss 7, p 828 (2024)
Alzheimer’s disease (AD) may manifest retinal changes preceding brain pathology. A transversal case-control study utilized spectral-domain OCT angiography (SD-OCTA) and Angio-Tool software 0.6a to assess retinal vascular structures and OCT for inne
Externí odkaz:
https://doaj.org/article/bceffc28deb94c739883335509abc02b
Autor:
Jose A. Fernández-Albarral, Ana I. Ramírez, Rosa de Hoz, José A. Matamoros, Elena Salobrar-García, Lorena Elvira-Hurtado, Inés López-Cuenca, Lidia Sánchez-Puebla, Juan J. Salazar, José M. Ramírez
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 18 (2024)
Glaucoma is a neurodegenerative disease of the retina characterized by the irreversible loss of retinal ganglion cells (RGCs) leading to visual loss. Degeneration of RGCs and loss of their axons, as well as damage and remodeling of the lamina cribros
Externí odkaz:
https://doaj.org/article/28a3dd901864465d868896fac6759e85
Autor:
Lorena Elvira-Hurtado, Inés López-Cuenca, Rosa de Hoz, Mario Salas, Lidia Sánchez-Puebla, Federico Ramírez-Toraño, José A. Matamoros, José A. Fernández-Albarral, Pilar Rojas, Soraya Alfonsín, María Luisa Delgado-Losada, Ana I. Ramírez, Juan J. Salazar, Fernando Maestu, Pedro Gil, José M. Ramírez, Elena Salobrar-García
Publikováno v:
Frontiers in Psychology, Vol 14 (2023)
IntroductionAlzheimer’s disease (AD) is the most common form of dementia affecting the central nervous system, and alteration of several visual structures has been reported. Structural retinal changes are usually accompanied by changes in visual fu
Externí odkaz:
https://doaj.org/article/29d307a4995a417399429a878183b989
Autor:
Lidia Sánchez-Puebla, Inés López-Cuenca, Elena Salobrar-García, Ana I. Ramírez, José A. Fernández-Albarral, José A. Matamoros, Lorena Elvira-Hurtado, Juan J. Salazar, José M. Ramírez, Rosa de Hoz
Publikováno v:
Biomedicines, Vol 12, Iss 3, p 528 (2024)
The murine models of Alzheimer’s disease (AD) have advanced our understanding of the pathophysiology. In vivo studies of the retina using optical coherence tomography (OCT) have complemented histological methods; however, the lack of standardisatio
Externí odkaz:
https://doaj.org/article/c6443dfe95444bb396119ce09df80050
Autor:
Inés López-Cuenca, Alberto Marcos-Dolado, Miguel Yus-Fuertes, Elena Salobrar-García, Lorena Elvira-Hurtado, José A. Fernández-Albarral, Juan J. Salazar, Ana I. Ramírez, Lidia Sánchez-Puebla, Manuel Enrique Fuentes-Ferrer, Ana Barabash, Federico Ramírez-Toraño, Lidia Gil-Martínez, Juan Arrazola-García, Pedro Gil, Rosa de Hoz, José M. Ramírez
Publikováno v:
Alzheimer’s Research & Therapy, Vol 14, Iss 1, Pp 1-18 (2022)
Abstract Background Two main genetic risks for sporadic Alzheimer’s disease (AD) are a family history and ɛ4 allele of apolipoprotein E. The brain and retina are part of the central nervous system and share pathophysiological mechanisms in AD. Met
Externí odkaz:
https://doaj.org/article/49329f36ef8c4e2d84f49e46a209ad7b
Autor:
Inés López-Cuenca, Lidia Sánchez-Puebla, Elena Salobrar-García, María Álvarez-Gutierrez, Lorena Elvira-Hurtado, Ana Barabash, Federico Ramírez-Toraño, José A. Fernández-Albarral, José A. Matamoros, Alberto Nebreda, Alejandra García-Colomo, Ana I. Ramírez, Juan J. Salazar, Pedro Gil, Fernando Maestú, José M. Ramírez, Rosa de Hoz
Publikováno v:
Biomedicines, Vol 11, Iss 7, p 2024 (2023)
This study aimed to analyze the evolution of visual changes in cognitively healthy individuals at risk for Alzheimer’s disease (AD). Participants with a first-degree family history of AD (FH+) and carrying the Ε4+ allele for the ApoE gene (ApoE ε
Externí odkaz:
https://doaj.org/article/ea301ad1b5a94688aecbd2ea5a9bb57a
Autor:
José A. Fernández-Albarral, Elena Salobrar-García, José A. Matamoros, Cristina Fernández-Mendívil, Eric del Sastre, Lejing Chen, Rosa de Hoz, Inés López-Cuenca, Lidia Sánchez-Puebla, José M. Ramírez, Juan J. Salazar, Manuela G. Lopez, Ana I. Ramírez
Publikováno v:
Antioxidants, Vol 11, Iss 11, p 2151 (2022)
Tauopathies such as Alzheimer’s disease are characterized by the accumulation of neurotoxic aggregates of tau protein. With aging and, especially, in Alzheimer’s patients, the inducible enzyme heme oxygenase 1 (HO-1) progressively increases in mi
Externí odkaz:
https://doaj.org/article/eac4377513624c96a1b40152ad8040ea
Autor:
Jose A. Fernández-Albarral, Rosa de Hoz, José A. Matamoros, Lejing Chen, Inés López-Cuenca, Elena Salobrar-García, Lidia Sánchez-Puebla, José M. Ramírez, Alberto Triviño, Juan J. Salazar, Ana I. Ramírez
Publikováno v:
Biomedicines, Vol 10, Iss 5, p 939 (2022)
Macroglia (astrocytes and Müller glia) may play an important role in the pathogenesis of glaucoma. In a glaucoma mouse model, we studied the effects of unilateral laser-induced ocular hypertension (OHT) on macroglia in OHT and contralateral eyes at
Externí odkaz:
https://doaj.org/article/6efd711f528f490da58ab95537da09b0
Autor:
Inés López-Cuenca, Elena Salobrar-García, Lorena Elvira-Hurtado, José A. Fernández-Albarral, Lidia Sánchez-Puebla, Juan J. Salazar, José M. Ramírez, Ana I. Ramírez, Rosa de Hoz
Publikováno v:
Life, Vol 11, Iss 7, p 712 (2021)
Preclinical Alzheimer’s disease (AD) includes cognitively healthy subjects with at least one positive biomarker: reduction in cerebrospinal fluid Aβ42 or visualization of cerebral amyloidosis by positron emission tomography imaging. The use of the
Externí odkaz:
https://doaj.org/article/53f81d389a71499dae4afbd38b994ddc
Autor:
Juan J. Salazar, Andrea Satriano, José A. Matamoros, José A. Fernández-Albarral, Elena Salobrar-García, Inés López-Cuenca, Rosa de Hoz, Lidia Sánchez-Puebla, José M. Ramírez, Cristina Alonso, Valentina Satta, Inés Hernández-Fisac, Onintza Sagredo, Ana I. Ramírez
Publikováno v:
International Journal of Molecular Sciences
Volume 24
Issue 3
Pages: 2727
Volume 24
Issue 3
Pages: 2727
Dravet syndrome (DS) is an epileptic encephalopathy caused by mutations in the Scn1a gene encoding the α1 subunit of the Nav1.1 sodium channel, which is associated with recurrent and generalized seizures, even leading to death. In experimental model
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::636fc02af934fd40989e57d083337d69
https://eprints.ucm.es/id/eprint/77258/
https://eprints.ucm.es/id/eprint/77258/
