Rey MJ - Search Results

1

A novel mutation in the PSEN1 gene (L286P) associated with familial early-onset dementia of Alzheimer type and lobar haematomas.

Sánchez-Valle R, Lladó A, Ezquerra M, Rey MJ, Rami L, Molinuevo JL. Sánchez-Valle R, et al. Among authors: rey mj. Eur J Neurol. 2007 Dec;14(12):1409-12. doi: 10.1111/j.1468-1331.2007.01988.x. Eur J Neurol. 2007. PMID: 18028191

2

Large APP locus duplication in a sporadic case of cerebral haemorrhage.

Lladó A, Grau-Rivera O, Sánchez-Valle R, Balasa M, Obach V, Amaro S, Rey MJ, Molinuevo JL, Gelpi E, Antonell A. Lladó A, et al. Among authors: rey mj. Neurogenetics. 2014 May;15(2):145-9. doi: 10.1007/s10048-014-0395-z. Epub 2014 Apr 2. Neurogenetics. 2014. PMID: 24691562

3

Late-onset frontotemporal dementia associated with a novel PGRN mutation.

Lladó A, Sánchez-Valle R, Reñé R, Ezquerra M, Rey MJ, Tolosa E, Ferrer I, Molinuevo JL. Lladó A, et al. Among authors: rey mj. J Neural Transm (Vienna). 2007;114(8):1051-4. doi: 10.1007/s00702-007-0716-6. Epub 2007 Apr 10. J Neural Transm (Vienna). 2007. PMID: 17417739

4

[New mutation in the PSEN1 (E120G) gene associated with early onset Alzheimer's disease].

Lladó A, Sánchez-Valle R, Rey MJ, Mercadal P, Almenar C, López-Villegas D, Fortea J, Molinuevo JL. Lladó A, et al. Among authors: rey mj. Neurologia. 2010 Jan-Feb;25(1):13-6. Neurologia. 2010. PMID: 20388456 Free article. Spanish.

5

Clinical features and APOE genotype of pathologically proven early-onset Alzheimer disease.

Balasa M, Gelpi E, Antonell A, Rey MJ, Sánchez-Valle R, Molinuevo JL, Lladó A; Neurological Tissue Bank/University of Barcelona/Hospital Clínic NTB/UB/HC Collaborative Group. Balasa M, et al. Among authors: rey mj. Neurology. 2011 May 17;76(20):1720-5. doi: 10.1212/WNL.0b013e31821a44dd. Neurology. 2011. PMID: 21576687

6

Diagnostic accuracy of behavioral variant frontotemporal dementia consortium criteria (FTDC) in a clinicopathological cohort.

Balasa M, Gelpi E, Martín I, Antonell A, Rey MJ, Grau-Rivera O, Molinuevo JL, Sánchez-Valle R, Lladó A; Catalan collaborative Study Group for FTLD. Balasa M, et al. Among authors: rey mj. Neuropathol Appl Neurobiol. 2015 Dec;41(7):882-92. doi: 10.1111/nan.12194. Epub 2015 May 2. Neuropathol Appl Neurobiol. 2015. PMID: 25381753

7

Primary progressive aphasia as the initial manifestation of corticobasal degeneration and unusual tauopathies.

Ferrer I, Hernández I, Boada M, Llorente A, Rey MJ, Cardozo A, Ezquerra M, Puig B. Ferrer I, et al. Among authors: rey mj. Acta Neuropathol. 2003 Nov;106(5):419-35. doi: 10.1007/s00401-003-0756-4. Epub 2003 Aug 29. Acta Neuropathol. 2003. PMID: 12955398

8

[MM1 variant of sporadic Creutzfeldt-Jakob disease with long duration akinetic mutism state].

Sanchez-Valle R, Santamaria J, Rey MJ, Rodriguez A, Graus F, Saiz A. Sanchez-Valle R, et al. Among authors: rey mj. Neurologia. 2006 Oct;21(8):444-6. Neurologia. 2006. PMID: 17013791 Spanish.

9

Parkinsonism, dysautonomia, REM behaviour disorder and visual hallucinations mimicking synucleinopathy in a patient with progressive supranuclear palsy.

Compta Y, Martí MJ, Rey MJ, Ezquerra M. Compta Y, et al. Among authors: rey mj. J Neurol Neurosurg Psychiatry. 2009 May;80(5):578-9. doi: 10.1136/jnnp.2007.142810. J Neurol Neurosurg Psychiatry. 2009. PMID: 19372296 No abstract available.

10

Hirano body-rich subtypes of Creutzfeldt-Jakob disease.

Martinez-Saez E, Gelpi E, Rey MJ, Ferrer I, Ribalta T, Botta-Orfila T, Nos C, Yagüe J, Sanchez-Valle R. Martinez-Saez E, et al. Among authors: rey mj. Neuropathol Appl Neurobiol. 2012 Apr;38(2):153-61. doi: 10.1111/j.1365-2990.2011.01208.x. Neuropathol Appl Neurobiol. 2012. PMID: 21726270

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