Zobrazeno 1 - 10
of 36
pro vyhledávání: '"M J, Rey"'
Autor:
J. Yagüe, M. J. Rey, Ellen Gelpi, Elena Martínez-Sáez, Carlos Nos, Isidro Ferrer, Teresa Ribalta, Raquel Sánchez-Valle, Teresa Botta-Orfila
Publikováno v:
Neuropathology and Applied Neurobiology. 38:153-161
E. Martinez-Saez, E. Gelpi, M. J. Rey, I. Ferrer, T. Ribalta, T. Botta-Orfila, C. Nos, J. Yague and R. Sanchez-Valle (2012) Neuropathology and Applied Neurobiology38, 153–161 Hirano body-rich subtypes of Creutzfeldt–Jakob disease Background: In d
Autor:
Ellen Gelpi, Albert Lladó, Raquel Sánchez-Valle, Anna Antonell, M. J. Rey, José Luis Molinuevo, Mircea Balasa
Publikováno v:
Neurology. 76:1720-1725
Objectives: Early-onset Alzheimer disease (EOAD) diagnosis often represents a challenge because of the high frequency of atypical presentations. Our aim was to describe the clinical features, APOE genotype, and its pathologic correlations of neuropat
Autor:
Albert Lladó, D. López-Villegas, Raquel Sánchez-Valle, Juan Fortea, C. Almenar, P. Mercadal, José Luis Molinuevo, M. J. Rey
Publikováno v:
Neurología (English Edition), Vol 25, Iss 1, Pp 13-16 (2010)
Objective: To describe a novel mutation in exon 5 of the presenilin 1 gene (E120G) associated with early-onset autosomal dominant Alzheimer's disease (AD). Patient and methods: The proband was a man who began with memory loss and progressive cognitiv
Autor:
M. J. Rey, C. Almenar, P. Mercadal, Raquel Sánchez-Valle, Albert Lladó, Juan Fortea, D. López-Villegas, José Luis Molinuevo
Publikováno v:
Neurología, Vol 25, Iss 1, Pp 13-16 (2010)
Resumen: Objetivo: Describir una nueva mutación en el exón 5 del gen PSEN1 (E120G) asociada a enfermedad de Alzheimer (EA) de inicio precoz y patrón de herencia autosómico dominante. Paciente y métodos: El probando era un varón en el que se ini
Autor:
M. J. Rey, Albert Lladó, José Luis Molinuevo, Mario Ezquerra, Lorena Rami, Raquel Sánchez-Valle
Publikováno v:
European Journal of Neurology. 14:1409-1412
The aim of this study was to describe a novel mutation in exon 8 of the presenilin gene (L286P) associated with early-onset autosomal dominant Alzheimer's disease (AD) and lobar haematomas. The proband was a woman who developed cognitive decline with
Autor:
E. Goutan, Francesc Viñals, Teresa Ribalta, R. Blanco, Berta Puig, Margarita Carmona, Isidro Ferrer, Adriana Cardozo, M. J. Rey, R. Ribera
Publikováno v:
Brain Pathol
Abnormal tau phosphorylation and deposition in neurones and glial cells is one of the major features in tau pathies. The present study examines the involvement of the Ras/MEK/ERK pathway of tau phosphorylation in Alzheimer disease (AD), Pick's diseas
Autor:
M. J. Rey, Eva Tolosa, Isidro Ferrer, Rafael Oliva, E. Pastor, Eva Muñoz, Berta Puig, Pau Pastor
Publikováno v:
Neuropathology and Applied Neurobiology. 29:23-34
Tau phosphorylation has been examined by immunohistochemistry in the brain of a patient affected with familial tauopathy with progressive supranuclear palsy-like phenotype linked to the delN296 mutation in the tau gene. Phospho-specific tau antibodie
Autor:
Sergio Amaro, Raquel Sánchez-Valle, Oriol Grau-Rivera, Ellen Gelpi, M. J. Rey, José Luis Molinuevo, Mircea Balasa, Albert Lladó, Anna Antonell, Victor Obach
Publikováno v:
Neurogenetics. 15(2)
We report a 54-year-old man who was admitted to the hospital because of acute neurological symptoms due to a cerebral haemorrhage. Postmortem brain examination revealed a lobar haemorrhage and advanced AD neuropathologic changes associated with sever
Publikováno v:
Brain Research. 866:257-261
Trophic factors, administered systemically or delivered via genetically-modified cells grafted into target regions, have been proposed as putative therapeutic agents in human neurodegenerative disorders. In parallel to the study of the beneficial eff
Autor:
Mircea, Balasa, Ellen, Gelpi, M J, Rey, Jordi, Vila, Lluís, Ramió-Torrentà, Ana Ma, Quiles Granado, Ricard, Molina Latorre, Hubert, Lepidi, Didier, Raoult, Albert, Saiz
Publikováno v:
Brain Pathol
Central nervous system Whipple's disease (CNS‐WD) with clinically isolated neurological involvement is a rare condition fatal without an early diagnosis. We aimed to present clinical and neuropathological features of three cases of pre‐ or post