Sánchez-Valle R - Search Results

1

A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain).

Palencia-Madrid L, Sánchez-Valle R, Fernández de Retana I, Borrego S, Grau-Rivera O, Reñé R, Hernández I, Almenar C, Rossi G, Caroppo P, Redaelli V, Le Ber I, Camuzat A, Brice A, Antonell A, Balasa M, Gelpi E, Lladó A, de Pancorbo MM. Palencia-Madrid L, et al. Neurobiol Aging. 2019 Dec;84:236.e9-236.e15. doi: 10.1016/j.neurobiolaging.2019.08.015. Epub 2019 Aug 21. Neurobiol Aging. 2019. PMID: 31537395

2

Ancestral origins of the prion protein gene D178N mutation in the Basque Country.

Rodríguez-Martínez AB, Barreau C, Coupry I, Yagüe J, Sánchez-Valle R, Galdós-Alcelay L, Ibáñez A, Digón A, Fernández-Manchola I, Goizet C, Castro A, Cuevas N, Alvarez-Alvarez M, de Pancorbo MM, Arveiler B, Zarranz JJ. Rodríguez-Martínez AB, et al. Hum Genet. 2005 Jun;117(1):61-9. doi: 10.1007/s00439-005-1277-0. Epub 2005 Apr 2. Hum Genet. 2005. PMID: 15806397

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. 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

Brain tau expression and correlation with the H1/H1 tau genotype in frontotemporal lobar degeneration patients.

Lladó A, Ezquerra M, Gaig C, Sánchez-Valle R, Tolosa E, Molinuevo JL. Lladó A, et al. J Neural Transm (Vienna). 2007;114(12):1585-8. doi: 10.1007/s00702-007-0786-5. Epub 2007 Jul 30. J Neural Transm (Vienna). 2007. PMID: 17661153

5

A novel MAPT mutation (P301T) associated with familial frontotemporal dementia.

Lladó A, Ezquerra M, Sánchez-Valle R, Rami L, Tolosa E, Molinuevo JL. Lladó A, et al. Eur J Neurol. 2007 Aug;14(8):e9-10. doi: 10.1111/j.1468-1331.2007.01763.x. Eur J Neurol. 2007. PMID: 17662000 No abstract available.

6

MAPT gene duplications are not a cause of frontotemporal lobar degeneration.

Lladó A, Rodríguez-Santiago B, Antonell A, Sánchez-Valle R, Molinuevo JL, Reñé R, Pérez-Jurado LA. Lladó A, et al. Neurosci Lett. 2007 Aug 31;424(1):61-5. doi: 10.1016/j.neulet.2007.07.008. Epub 2007 Aug 1. Neurosci Lett. 2007. PMID: 17707586

7

Longitudinal study of amnesic patients at high risk for Alzheimer's disease: clinical, neuropsychological and magnetic resonance spectroscopy features.

Rami L, Gómez-Anson B, Sanchez-Valle R, Bosch B, Monte GC, Lladó A, Molinuevo JL. Rami L, et al. Dement Geriatr Cogn Disord. 2007;24(5):402-10. doi: 10.1159/000109750. Epub 2007 Oct 12. Dement Geriatr Cogn Disord. 2007. PMID: 17934274

8

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. Eur J Neurol. 2007 Dec;14(12):1409-12. doi: 10.1111/j.1468-1331.2007.01988.x. Eur J Neurol. 2007. PMID: 18028191

9

Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation.

Rodríguez-Martínez AB, Alfonso-Sánchez MA, Peña JA, Sánchez-Valle R, Zerr I, Capellari S, Calero M, Zarranz JJ, de Pancorbo MM. Rodríguez-Martínez AB, et al. Neurogenetics. 2008 May;9(2):109-18. doi: 10.1007/s10048-008-0120-x. Epub 2008 Mar 18. Neurogenetics. 2008. PMID: 18347820

10

Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration.

Lladó A, Sánchez-Valle R, Rey MJ, Ezquerra M, Tolosa E, Ferrer I, Molinuevo JL; Catalan collaborative Study Group for FTLD. Lladó A, et al. J Neurol. 2008 Apr;255(4):488-94. doi: 10.1007/s00415-008-0565-8. Epub 2008 Mar 25. J Neurol. 2008. PMID: 18357425

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