Results 21 to 30 of about 19,000 (208)

ENFERMEDADES NEURODEGENERATIVAS; ASPECTOS NUTRICIONALES

NUTRICION HOSPITALARIA, 2015
Introduction: neurodegenerative diseases cause changes in the level of consciousness or swallowing mechanisms that often necessitate a specialized nutritional support. Objective: review the risk of malnutrition and its treatment in patients with cerebral vascular disease, Parkinson’s disease, dementia and amyotrophic lateral sclerosis ...
Luis, Daniel A. de, Izaola, Olatz, Fuente, Beatriz de la, Muñoz-Calero, Paloma, Franco-Lopez, Angeles   +4 more
openaire   +4 more sources

Relationship between the type and side of motor symptoms with the prevalence of non-motor symptoms in Parkinson's disease

Neurología (English Edition), 2011
Introduction: The relationship between laterality and asymmetry of Parkinson's disease and non-motor dysfunction has been studied mainly from the perspective of cognitive functions, and the few studies that have included other symptoms have mixed reports.
M. Rodríguez-Violante, A. Cervantes-Arriaga, A. Villar-Velarde, T. Corona   +3 more
doaj   +1 more source

Relación entre el tipo y lado de inicio de la sintomatología motora con la frecuencia de síntomas no motores en la enfermedad de Parkinson

Neurología, 2011
Resumen: Introducción: la relación de la lateralidad y asimetría de la enfermedad de Parkinson con la sintomatología de disfunción no motora ha sido abordada principalmente desde el punto de vista de las funciones cognitivas, y los escasos estudios que ...
M. Rodríguez-Violante, A. Cervantes-Arriaga, A. Villar-Velarde, T. Corona   +3 more
doaj   +1 more source

Estudio y manejo de las neuropatías de fibra fina

Kranion, 2022
La neuropatía de fibra fina es una entidad frecuentemente infradiagnosticada que puede deberse a numerosas causas. La sintomatología más habitual la conforman alteraciones de la sensibilidad y el dolor, síntomas disautonómicos como la taquicardia ...
Juan Carlos Gómez Esteban, Beatriz Tijero Merino, Sara Teijeira-Portas, Naiara Azkue   +3 more
doaj   +1 more source

Expression of the Adenosine A_2A-A₃ Receptor Heteromer in Different Brain Regions and Marked Upregulation in the Microglia of the Transgenic APP_Sw,Ind Alzheimer’s Disease Model

Biomedicines, 2022
Adenosine (Ado) receptors have been instrumental in the detection of heteromers and other higher-order receptor structures, mainly via interactions with other cell surface G-protein-coupled receptors.
Alejandro Lillo, Iu Raïch, Jaume Lillo, Catalina Pérez-Olives, Gemma Navarro, Rafael Franco   +5 more
doaj   +1 more source

Els processos neuroinflamatoris associats a les malalties neurodegeneratives. Si se m’inflama el cervell, se m’oblida el teu nom? [PDF]

, 2016
Aquest assaig és una revisió sobre els processos neuroinflamatoris que esdevenen en les malalties neurodegeneratives. Es descriuen les diferents estructures cel·lulars que trobem en el sistema nerviós, i farem especial èmfasi en les cèl·lules de ...
Ros Bernal, Francisco
core   +1 more source

CALBINDIN CONTENT AND DIFFERENTIAL VULNERABILITY OF MIDBRAIN EFFERENT DOPAMINERGIC NEURONS IN MACAQUES

Frontiers in Neuroanatomy, 2014
Calbindin (CB) is a calcium binding protein reported to protect dopaminergic neurons from degeneration. Although a direct link between CB content and differential vulnerability of dopaminergic neurons has long been accepted, factors other than CB have ...
Iria G Dopeso-Reyes, Iria G Dopeso-Reyes, Alberto J Rico, Alberto J Rico, Elvira eRoda, Elvira eRoda, Salvador eSierra-San Nicolas, Salvador eSierra-San Nicolas, Diego ePignataro, Diego ePignataro, Maria eLanz, Diego eSucunza, Luis eChang-Azancot, Jose L Lanciego, Jose L Lanciego   +14 more
doaj   +1 more source

Creutzfeldt-Jakob disease in Peru: report of eleven cases

Revista Peruana de Medicina Experimental y Salud Pública, 2014
Creutzfeldt-Jakob disease (CJD) is a fatal neurological disease caused by pathological isoform of the human prion protein. Clinical features of six cases of the sporadic form of CJD with definitive diagnosis by histopathology, and five cases with ...
Luis Torres-Ramírez, Jorge Ramírez-Quiñones, Carlos Cosentino-Esquerre, Miriam Vélez-Rojas, Martha Flores-Mendoza, Diana Rivas-Franchini, Rafael Suarez-Reyes, Yesenia Núñez-Coronado   +7 more
doaj   +1 more source

Additional mechanisms conferring genetic susceptibility to Alzheimer's disease

Frontiers in Cellular Neuroscience, 2015
Familial Alzheimer's disease (AD), mostly associated with early onset, is caused by mutations in three genes (APP, PSEN1 and PSEN2) involved in the production of the amyloid  peptide.
Miguel eCalero, Miguel eCalero, Miguel eCalero, Alberto eGomez-Ramos, Alberto eGomez-Ramos, Olga eCalero, Olga eCalero, Eduardo eSoriano, Eduardo eSoriano, Jesus eAvila, Jesus eAvila, Miguel eMedina, Miguel eMedina   +12 more
doaj   +1 more source

Cross-communication between Gi and Gs in a G-protein-coupled receptor heterotetramer guided by a receptor C-terminal domain

BMC Biology, 2018
Background G-protein-coupled receptor (GPCR) heteromeric complexes have distinct properties from homomeric GPCRs, giving rise to new receptor functionalities.
Gemma Navarro, Arnau Cordomí, Marc Brugarolas, Estefanía Moreno, David Aguinaga, Laura Pérez-Benito, Sergi Ferre, Antoni Cortés, Vicent Casadó, Josefa Mallol, Enric I. Canela, Carme Lluís, Leonardo Pardo, Peter J. McCormick, Rafael Franco   +14 more
doaj   +1 more source