Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Marta Galdós"'
Autor:
David Romero-Bascones, Unai Ayala, Ane Alberdi, Asier Erramuzpe, Marta Galdós, Juan Carlos Gómez-Esteban, Ane Murueta-Goyena, Sara Teijeira, Iñigo Gabilondo, Maitane Barrenechea
Publikováno v:
PLoS ONE, Vol 17, Iss 12 (2022)
Characterizing the effect of age and sex on macular retinal layer thicknesses and foveal pit morphology is crucial to differentiating between natural and disease-related changes. We applied advanced image analysis techniques to optical coherence tomo
Externí odkaz:
https://doaj.org/article/233bd224344d4e5da9ca4459bc71d133
Autor:
Olaia Lucas-Jiménez, Naroa Ibarretxe-Bilbao, Ibai Diez, Javier Peña, Beatriz Tijero, Marta Galdós, Ane Murueta-Goyena, Rocío Del Pino, Marian Acera, Juan Carlos Gómez-Esteban, Iñigo Gabilondo, Natalia Ojeda
Publikováno v:
Biomedicines, Vol 11, Iss 2, p 573 (2023)
Background: We aimed to characterize subtypes of synucleinopathies using a clustering approach based on cognitive and other nonmotor data and to explore structural and functional magnetic resonance imaging (MRI) brain differences between identified c
Externí odkaz:
https://doaj.org/article/252040bc2c4c4b598672808f5d8e2620
Autor:
David Romero-Bascones, Maitane Barrenechea, Ane Murueta-Goyena, Marta Galdós, Juan Carlos Gómez-Esteban, Iñigo Gabilondo, Unai Ayala
Publikováno v:
Entropy, Vol 23, Iss 6, p 699 (2021)
Disentangling the cellular anatomy that gives rise to human visual perception is one of the main challenges of ophthalmology. Of particular interest is the foveal pit, a concave depression located at the center of the retina that captures light from
Externí odkaz:
https://doaj.org/article/42b45afacee842ba8b18effe2a0077de
Autor:
Jesús Barrio-Barrio, Elvira Bonet-Farriol, Marta Galdós, Susana Noval, Victoria Pueyo, Charles E. Breeze, Jose Luis Santos, Belén Alfonso-Bartolozzi, Sergio Recalde, Ana Patiño-García
Publikováno v:
Journal of Ophthalmology, Vol 2019 (2019)
Introduction. Even though ocular refractive state is highly heritable and under strong genetic control, the identification of susceptibility genes remains a challenge. Several HGF (hepatocyte growth factor) gene variants have been associated with ocu
Externí odkaz:
https://doaj.org/article/a1826e5b2c00401b83d89f4957b2f5b5
Autor:
María Tarilonte, Matías Morín, Patricia Ramos, Marta Galdós, Fiona Blanco-Kelly, Cristina Villaverde, Dolores Rey-Zamora, Gema Rebolleda, Francisco J. Muñoz-Negrete, Saoud Tahsin-Swafiri, Blanca Gener, Miguel-Angel Moreno-Pelayo, Carmen Ayuso, Manuela Villamar, Marta Corton
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Mutations in PAX6 are involved in several developmental eye disorders. These disorders have considerable phenotypic variability, ranging from panocular forms of congenital aniridia and microphthalmia to isolated anomalies of the anterior or posterior
Externí odkaz:
https://doaj.org/article/801dfb1417c14445be3ac489617f1f8a
Autor:
María, Tarilonte, Matías, Morín, Patricia, Ramos, Marta, Galdós, Fiona, Blanco-Kelly, Cristina, Villaverde, Dolores, Rey-Zamora, Gema, Rebolleda, Francisco J, Muñoz-Negrete, Saoud, Tahsin-Swafiri, Blanca, Gener, Miguel-Angel, Moreno-Pelayo, Carmen, Ayuso, Manuela, Villamar, Marta, Corton
Publikováno v:
Frontiers in Genetics
Mutations in PAX6 are involved in several developmental eye disorders. These disorders have considerable phenotypic variability, ranging from panocular forms of congenital aniridia and microphthalmia to isolated anomalies of the anterior or posterior
Autor:
M. Aranzazu Goicolea, Marta Galdós, Alicia Sánchez-Ortega, Fernando Andrade, Ramón J. Barrio, Luis Aldámiz-Echevarría, Marta Llarena, Sergio Pinar-Sueiro
Publikováno v:
Metabolomics. 11:468-476
Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION) is a rare ischemic disease that affects the optic nerve. Pathophysiology and mechanism of ischemia of NAION remain uncertain, so the aim of this work is to establish the first metabolic fingerp
Autor:
Arantxa Acera, Juan Carlos Gómez-Esteban, Ane Murueta-Goyena, Marta Galdos, Mikel Azkargorta, Felix Elortza, Noelia Ruzafa, Oliver Ibarrondo, Xandra Pereiro, Elena Vecino
Publikováno v:
Proteomes, Vol 10, Iss 1, p 4 (2022)
Parkinson’s disease (PD) is the second most common neurodegenerative disease after Alzheimer’s disease. In this study, the tear proteome profile of patients with idiopathic PD (iPD, n = 24), carriers of the E46K-SNCA mutation (n = 3) and healthy
Externí odkaz:
https://doaj.org/article/640d0cb78c6d49408d8c507991e5d4d4