Zobrazeno 1 - 10
of 17
pro vyhledávání: '"M.M. Carmona-Abellán"'
Autor:
S. Ortega-Cubero, M.R. Luquín, I. Domínguez, J. Arbizu, I. Pagola, M.M. Carmona-Abellán, M. Riverol
Publikováno v:
Neurología, Vol 28, Iss 5, Pp 299-308 (2013)
Resumen: Introducción: Las prionopatías son un conjunto de enfermedades neurodegenerativas producidas por el acúmulo de una isoforma anormal de la proteína priónica celular (PrPc). Se clasifican en adquiridas, hereditarias y esporádicas. Aunque
Externí odkaz:
https://doaj.org/article/6da36594cad549cba97e218678b36e82
Autor:
S. Ortega-Cubero, M.R. Luquín, I. Domínguez, J. Arbizu, I. Pagola, M.M. Carmona-Abellán, M. Riverol
Publikováno v:
Neurología (English Edition), Vol 28, Iss 5, Pp 299-308 (2013)
Introduction: Prion diseases are neurodegenerative disorders resulting from the accumulation of a misfolded isoform of the cellular prion protein (PrPC). They can occur as acquired, sporadic, or hereditary forms. Although prion diseases show a wide r
Externí odkaz:
https://doaj.org/article/8bdf0dd9f9af49a5ba313d78367eb64d
Autor:
Maria-Teresa Tuñon, Carlos E. de Andrea, Rafael Valenti-Azcarate, Maria-Rosario Luquin, Mario Riverol, Ivan Martinez-Valbuena, Juan A. Sánchez-Arias, Irene Marcilla, Irene Amat-Villegas, M.M. Carmona-Abellán, Eduardo Martínez-Vila, Maria-Elena Erro, Gloria Marti
Publikováno v:
Annals of Neurology. 86:539-551
Objective Alzheimer disease (AD) is the leading cause of dementia, and although its etiology remains unclear, it seems that type 2 diabetes mellitus (T2DM) and other prediabetic states of insulin resistance could contribute to the appearance of spora
Autor:
Maria-Rosario Luquin, Irene Amat-Villegas, Maria-Teresa Tuñon, M.M. Carmona-Abellán, Irene Marcilla, Ivan Martinez-Valbuena, Rafael Valenti-Azcarate
Publikováno v:
Acta neuropathologica. 135(6)
Parkinson's disease patients experience a wide range of non-motor symptoms that may be provoked by deposits of phosphorylated α-synuclein in the peripheral nervous system. Pre-existing diabetes mellitus might be a risk factor for developing Parkinso
Autor:
M.M. Carmona-Abellán, I. Domínguez, Sara Ortega-Cubero, Javier Arbizu, I. Pagola, Mario Riverol, Maria-Rosario Luquin
Publikováno v:
Neurología (English Edition), Vol 28, Iss 5, Pp 299-308 (2013)
Introduction: Prion diseases are neurodegenerative disorders resulting from the accumulation of a misfolded isoform of the cellular prion protein (PrPC). They can occur as acquired, sporadic, or hereditary forms. Although prion diseases show a wide r
Autor:
José L. Lanciego, Maria-Rosario Luquin, María J. Blanco-Prieto, M.M. Carmona-Abellán, Hugo Lana, Irene Marcilla, Eduardo Ansorena, Elisa Garbayo
Publikováno v:
Biomaterials. 110
Glial cell line-derived neurotrophic factor (GDNF) remains the most potent neurotrophic factor for dopamine neurons. Despite its potential as treatment for Parkinson's disease (PD), its clinical application has been hampered by safety and efficacy co
Autor:
Robert Teasell, Sara Ortega-Cubero, M.M. Carmona-Abellán, Manuel Murie-Fernandez, Matthew Meyer
Publikováno v:
Neurología (English Edition), Vol 27, Iss 4, Pp 197-201 (2012)
Introduction and objective: In Spain, stroke is the leading cause of death in women as well as the leading cause of disability in adults. This translates into a huge human and economic cost. In recent years there have been significant advances both i
Autor:
M.M. Carmona-Abellán, Carlos Rodríguez-Nogales, María J. Blanco-Prieto, Elisa Garbayo, Maria-Rosario Luquin
Publikováno v:
Maturitas. 84
The etiology and pathogenesis of Parkinson's disease (PD) is unknown, aging being the strongest risk factor for brain degeneration. Understanding PD pathogenesis and how aging increases the risk of disease would aid the development of therapies able
Autor:
M. Rivero, Maria-Rosario Luquin, I. Lamet, N. Pujol Giménez, M.M. Carmona-Abellán, P. Esteve-Belloch
Publikováno v:
Anales del Sistema Sanitario de Navarra v.38 n.1 2015
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
Dadun. Depósito Académico Digital de la Universidad de Navarra
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
Dadun. Depósito Académico Digital de la Universidad de Navarra
La degeneración lobar frontotemporal engloba tres síndromes diferentes, que comparten características clínicas y patológicas comunes, dificultando así su diagnóstico en estadios iniciales. Se incluyen en este grupo las tres variantes de la dem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16c4a008bde730e770494ee423e16a13
http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1137-66272015000100009
http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1137-66272015000100009
Autor:
Sara Ortega-Cubero, M.M. Carmona-Abellán, Matthew Meyer, Manuel Murie-Fernandez, Robert Teasell
Publikováno v:
Dadun. Depósito Académico Digital de la Universidad de Navarra
instname
Neurología, Vol 27, Iss 4, Pp 197-201 (2012)
instname
Neurología, Vol 27, Iss 4, Pp 197-201 (2012)
Resumen: Introducción y objetivo: El ictus representa en España la primera causa de muerte por entidades específicas en mujeres, la primera causa de invalidez en los adultos y supone un enorme coste tanto humano como económico. En los últimos a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a9c1ac2ab6581feafdeeb7837c96e4d
https://hdl.handle.net/10171/22849
https://hdl.handle.net/10171/22849