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Hereditary Human Prion Diseases: an Update.
Schmitz M, Dittmar K, Llorens F, Gelpi E, Ferrer I, Schulz-Schaeffer WJ, Zerr I. Schmitz M, et al. Among authors: ferrer i. Mol Neurobiol. 2017 Aug;54(6):4138-4149. doi: 10.1007/s12035-016-9918-y. Epub 2016 Jun 20. Mol Neurobiol. 2017. PMID: 27324792 Free article. Review.
"Preclinical" MSA in definite Creutzfeldt-Jakob disease.
Rodriguez-Diehl R, Rey MJ, Gironell A, Martinez-Saez E, Ferrer I, Sánchez-Valle R, Jagüe J, Nos C, Gelpi E. Rodriguez-Diehl R, et al. Among authors: ferrer i. Neuropathology. 2012 Apr;32(2):158-63. doi: 10.1111/j.1440-1789.2011.01232.x. Epub 2011 Jun 21. Neuropathology. 2012. PMID: 21692862
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: ferrer i. Neuropathol Appl Neurobiol. 2012 Apr;38(2):153-61. doi: 10.1111/j.1365-2990.2011.01208.x. Neuropathol Appl Neurobiol. 2012. PMID: 21726270
Neuropathology of the hippocampus in FTLD-Tau with Pick bodies: a study of the BrainNet Europe Consortium.
Kovacs GG, Rozemuller AJ, van Swieten JC, Gelpi E, Majtenyi K, Al-Sarraj S, Troakes C, Bódi I, King A, Hortobágyi T, Esiri MM, Ansorge O, Giaccone G, Ferrer I, Arzberger T, Bogdanovic N, Nilsson T, Leisser I, Alafuzoff I, Ironside JW, Kretzschmar H, Budka H. Kovacs GG, et al. Among authors: ferrer i. Neuropathol Appl Neurobiol. 2013 Feb;39(2):166-78. doi: 10.1111/j.1365-2990.2012.01272.x. Neuropathol Appl Neurobiol. 2013. PMID: 22471883
Phenotypic variability within the inclusion body spectrum of basophilic inclusion body disease and neuronal intermediate filament inclusion disease in frontotemporal lobar degenerations with FUS-positive inclusions.
Gelpi E, Lladó A, Clarimón J, Rey MJ, Rivera RM, Ezquerra M, Antonell A, Navarro-Otano J, Ribalta T, Piñol-Ripoll G, Pérez A, Valldeoriola F, Ferrer I. Gelpi E, et al. Among authors: ferrer i. J Neuropathol Exp Neurol. 2012 Sep;71(9):795-805. doi: 10.1097/NEN.0b013e318266efb1. J Neuropathol Exp Neurol. 2012. PMID: 22892522
Distinct patterns of APP processing in the CNS in autosomal-dominant and sporadic Alzheimer disease.
Pera M, Alcolea D, Sánchez-Valle R, Guardia-Laguarta C, Colom-Cadena M, Badiola N, Suárez-Calvet M, Lladó A, Barrera-Ocampo AA, Sepulveda-Falla D, Blesa R, Molinuevo JL, Clarimón J, Ferrer I, Gelpi E, Lleó A. Pera M, et al. Among authors: ferrer i. Acta Neuropathol. 2013 Feb;125(2):201-13. doi: 10.1007/s00401-012-1062-9. Epub 2012 Dec 6. Acta Neuropathol. 2013. PMID: 23224319 Free PMC article.
1,334 results