Oriol Grau‐Rivera

发表

Cerebrospinal Fluid Biomarkers Predict Clinical Evolution in Patients with Subjective Cognitive Decline and Mild Cognitive Impairment

J. Molinuevo, B. Bosch, L. Rami, 2015, Neurodegenerative Diseases.

Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease

M. Tsolaki, K. Sleegers, C. van Broeckhoven, 2017, Acta Neuropathologica.

Systematic Screening of Ubiquitin/p62 Aggregates in Cerebellar Cortex Expands the Neuropathological Phenotype of the C9orf72 Expansion Mutation

J. Clarimón, P. Pástor, D. Lopez-Villegas, 2018, Journal of neuropathology and experimental neurology.

Determination of neuronal antibodies in suspected and definite Creutzfeldt-Jakob disease.

J. Molinuevo, R. Sánchez-Valle, A. Saiz, 2014, JAMA neurology.

Clinicopathological Correlations and Concomitant Pathologies in Rapidly Progressive Dementia: A Brain Bank Series

J. Molinuevo, I. Ferrer, R. Sánchez-Valle, 2015, Neurodegenerative Diseases.

Altered mechanisms of protein synthesis in frontal cortex in Alzheimer disease and a mouse model.

I. Ferrer, T. Sklaviadis, E. Gelpí, 2017, American journal of neurodegenerative disease.

Prevalence of amyloid‐β pathology in distinct variants of primary progressive aphasia

Nick C Fox, W. M. van der Flier, S. Black, 2018, Annals of neurology.

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease

Giuliano Binetti, Alberto Lleó, Juan Fortea, 2016, Acta Neuropathologica.

Pisa syndrome in a patient with pathologically confirmed Parkinson's disease

F. Marrosu, M. Marti, P. Solla, 2016, Neuropathology and applied neurobiology.

PrP mRNA and protein expression in brain and PrPc in CSF in Creutzfeldt-Jakob disease MM1 and VV2

J. Yagüe, J. D. del Río, I. Zerr, 2013, Prion.

Prominent psychiatric symptoms in patients with Parkinson’s disease and concomitant argyrophilic grain disease

E. Tolosa, F. Valldeoriola, Y. Compta, 2013, Journal of Neurology.

Frontotemporal Dementia Caused by the P301L Mutation in the MAPT Gene: Clinicopathological Features of 13 Cases from the Same Geographical Origin in Barcelona, Spain

J. Molinuevo, R. Sánchez-Valle, I. Hernández, 2017, Dementia and Geriatric Cognitive Disorders.

Subtype and regional regulation of prion biomarkers in sporadic Creutzfeldt–Jakob disease

I. Zerr, F. Llorens, I. Ferrer, 2015, Neuropathology and applied neurobiology.

Regional Overlap of Pathologies in Lewy Body Disorders

E. Tolosa, J. Kulisevsky, J. Clarimón, 2017, Journal of neuropathology and experimental neurology.

Analysis of known amyotrophic lateral sclerosis and frontotemporal dementia genes reveals a substantial genetic burden in patients manifesting both diseases not carrying the C9orf72 expansion mutation

J. Clarimón, A. Lleó, R. Blesa, 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

Structural Connectivity Alterations Along the Alzheimer’s Disease Continuum: Reproducibility Across Two Independent Samples and Correlation with Cerebrospinal Fluid Amyloid-β and Tau

J. Molinuevo, A. Tucholka, C. Falcón, 2018, Journal of Alzheimer's disease : JAD.