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Page 1
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: rene r. 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
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. Among authors: rene r. 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
Frontotemporal Dementia Caused by the P301L Mutation in the MAPT Gene: Clinicopathological Features of 13 Cases from the Same Geographical Origin in Barcelona, Spain.
Borrego-Écija S, Morgado J, Palencia-Madrid L, Grau-Rivera O, Reñé R, Hernández I, Almenar C, Balasa M, Antonell A, Molinuevo JL, Lladó A, Martínez de Pancorbo M, Gelpi E, Sánchez-Valle R. Borrego-Écija S, et al. Among authors: rene r. Dement Geriatr Cogn Disord. 2017;44(3-4):213-221. doi: 10.1159/000480077. Epub 2017 Sep 22. Dement Geriatr Cogn Disord. 2017. PMID: 28934750
Neuroimaging and biochemical markers in the three variants of primary progressive aphasia.
Gil-Navarro S, Lladó A, Rami L, Castellví M, Bosch B, Bargalló N, Lomeña F, Reñé R, Montagut N, Antonell A, Molinuevo JL, Sánchez-Valle R. Gil-Navarro S, et al. Among authors: rene r. Dement Geriatr Cogn Disord. 2013;35(1-2):106-17. doi: 10.1159/000346289. Epub 2013 Feb 6. Dement Geriatr Cogn Disord. 2013. PMID: 23392204
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. Among authors: rene r. 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
Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes.
Thelen M, Razquin C, Hernández I, Gorostidi A, Sánchez-Valle R, Ortega-Cubero S, Wolfsgruber S, Drichel D, Fliessbach K, Duenkel T, Damian M, Heilmann S, Slotosch A, Lennarz M, Seijo-Martínez M, Rene R, Kornhuber J, Peters O, Luckhaus C, Jahn H, Hüll M, Rüther E, Wiltfang J, Lorenzo E, Gascon J, Lleó A, Lladó A, Campdelacreu J, Moreno F, Ahmadzadehfar H; Dementia Genetics Spanish Consortium (DEGESCO); Fortea J, Indakoetxea B, Heneka MT, Wetter A, Pastor MA, Riverol M, Becker T, Frölich L, Tárraga L, Boada M, Wagner M, Jessen F, Maier W, Clarimón J, López de Munain A, Ruiz A, Pastor P, Ramirez A. Thelen M, et al. Among authors: rene r. Neurobiol Aging. 2014 Nov;35(11):2657.e13-2657.e19. doi: 10.1016/j.neurobiolaging.2014.06.018. Epub 2014 Jun 20. Neurobiol Aging. 2014. PMID: 25042114
101 results