Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Jose Enrique De La Rubia"'
Autor:
Jose Enrique de la Rubia Ortí, María Pilar García-Pardo, María Cuerda-Ballester, Gloria Castellano-Estornell, María Benlloch
Publikováno v:
Frontiers in Nutrition, Vol 11 (2024)
Externí odkaz:
https://doaj.org/article/104fc8680368486daee284aa65d9a5a1
Autor:
Belén Proaño, María Benlloch, Sandra Sancho-Castillo, Jesús Privado, Guillermo Bargues-Navarro, Claudia Emmanuela Sanchis-Sanchis, Palmira Martínez Bolós, Ana Belén Carriquí-Suárez, Laura Cubero-Plazas, Jose Luis Platero Armero, Dolores Escriva, Jose Joaquín Ceron, Asta Tvarijonaviciute, Jose Enrique de la Rubia Ortí
Publikováno v:
Antioxidants, Vol 13, Iss 8, p 1021 (2024)
Background: Amyotrophic lateral sclerosis (ALS) is characterized by progressive motor neuron degeneration, with oxidative stress playing a key role. Paraoxonase 1 (PON1) is an antioxidant enzyme that may influence ALS progression. This study aimed to
Externí odkaz:
https://doaj.org/article/99befc0c5bbe4c21bcd6dc81b05265b6
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Background and Objective: Multimodal management of spinal stenosis is on the rise, and central sensitisation inhibitors are playing an essential role in the treatment of central sensitisation processes. Pregabalin and gabapentin are antiepileptic dru
Externí odkaz:
https://doaj.org/article/7bb0d0a177544114a56528a53be52c28
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionThis study aimed to investigate the incidence of vitamin D deficiency in patients with adolescent idiopathic scoliosis through a meta-analysis and to analyze trends and risk factors.MethodsPotentially relevant studies were searched using
Externí odkaz:
https://doaj.org/article/e62bf1741b5546159de2c726a903197c
Autor:
Jose Enrique de la Rubia Ortí, María Cuerda-Ballester, Claudia Emmanuela Sanchis-Sanchis, Jose María Lajara Romance, Esther Navarro-Illana, María Pilar García Pardo
Publikováno v:
Frontiers in Nutrition, Vol 10 (2023)
BackgroundMultiple sclerosis (MS) is a neurodegenerative disorder. Individuals with MS frequently present symptoms such as functional disability, obesity, and anxiety and depression. Axonal demyelination can be observed and implies alterations in mit
Externí odkaz:
https://doaj.org/article/09f32187a3d8494886ddbb2e8e172fbf
Autor:
Jose Enrique de la Rubia Ortí, Jose Luis Platero Armero, María Cuerda-Ballester, Claudia Emmanuela Sanchis-Sanchis, Esther Navarro-Illana, Jose María Lajara-Romance, María Benlloch, Jose Joaquín Ceron, Asta Tvarijonaviciute, Belén Proaño
Publikováno v:
Foods, Vol 12, Iss 20, p 3730 (2023)
Background: Multiple sclerosis (MS) patients present dyslipidemia and functional disability. Epigallocatechin gallate (EGCG) and coconut oil have been shown to be effective against dyslipidemia. Objective: To analyze the relationship between lipid pr
Externí odkaz:
https://doaj.org/article/11e76f39cd574e32b8d26a0af4cb708c
Publikováno v:
Frontiers in Nutrition, Vol 8 (2021)
Background: Alzheimer's disease is the most common neurodegenerative disorder in our society, mainly characterized by loss of cognitive function. However, other symptoms such as anxiety and depression have been described in patients. The process is m
Externí odkaz:
https://doaj.org/article/fcb24a9b103b46e588826fbb23aac5d6
Autor:
Jorge Alarcón-Jimenez, Jose Enrique de la Rubia Ortí, Julio Martín Ruiz, Nieves de Bernardo, Belén Proaño, Carlos Villarón-Casales
Publikováno v:
Life, Vol 12, Iss 12, p 1978 (2022)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative and fatal disease, characterized by the loss of motor neurons and progressive musculoskeletal deterioration. The clinical onset is mainly bulbar or spinal. Considering that there is no effect
Externí odkaz:
https://doaj.org/article/a5fa7e2f20814c8ba606f290df3da362
Autor:
Belén Proaño, Julia Casani-Cubel, María Benlloch, Ana Rodriguez-Mateos, Esther Navarro-Illana, Jose María Lajara-Romance, Jose Enrique de la Rubia Ortí
Publikováno v:
Biomedicines, Vol 10, Iss 9, p 2084 (2022)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that is characterized by the loss of upper and lower motor neurons (MNs) in the cerebral cortex, brainstem and spinal cord, with consequent weakness, atrophy and the progressive paral
Externí odkaz:
https://doaj.org/article/60b5b96754994a52af800b213f066b62
Autor:
Sandra Carrera-Juliá, Mari Luz Moreno, Carlos Barrios, Jose Enrique de la Rubia Ortí, Eraci Drehmer
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that produces a selective loss of the motor neurons of the spinal cord, brain stem and motor cortex. Oxidative stress (OS) associated with mitochondrial dysfunction and the deteriorat
Externí odkaz:
https://doaj.org/article/4ac8d60308e44499a80521fd3e44f145