Ferrer I - Search Results

1

Variably protease-sensitive prionopathy presenting within ALS/FTD spectrum.

Vicente-Pascual M, Rossi M, Gámez J, Lladó A, Valls J, Grau-Rivera O, Ávila Polo R, Llorens F, Zerr I, Ferrer I, Nos C, Parchi P, Sánchez-Valle R, Gelpí E. Vicente-Pascual M, et al. Among authors: ferrer i. Ann Clin Transl Neurol. 2018 Sep 21;5(10):1297-1302. doi: 10.1002/acn3.632. eCollection 2018 Oct. Ann Clin Transl Neurol. 2018. PMID: 30349865 Free PMC article.

2

Ubiquitin in cerebral amyloid angiopathy.

Cruz-Sanchez FF, Marin C, Rossi ML, Cardozo A, Ferrer I, Tolosa E. Cruz-Sanchez FF, et al. Among authors: ferrer i. J Neurol Sci. 1992 Oct;112(1-2):46-50. doi: 10.1016/0022-510x(92)90130-d. J Neurol Sci. 1992. PMID: 1335037

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: ferrer i. 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

Chorea-ballism associated with familial amyotrophic lateral sclerosis. A clinical, genetic, and neuropathological study.

Gamez J, Corbera-Bellalta M, Mila M, López-Lisbona R, Boluda S, Ferrer I. Gamez J, et al. Among authors: ferrer i. Mov Disord. 2008 Feb 15;23(3):434-8. doi: 10.1002/mds.21856. Mov Disord. 2008. PMID: 18072201

5

Clinical and pathological heterogeneity of neuronal intermediate filament inclusion disease.

Molina-Porcel L, Lladó A, Rey MJ, Molinuevo JL, Martinez-Lage M, Esteve FX, Ferrer I, Tolosa E, Blesa R. Molina-Porcel L, et al. Among authors: ferrer i. Arch Neurol. 2008 Feb;65(2):272-5. doi: 10.1001/archneurol.2007.37. Arch Neurol. 2008. PMID: 18268200

6

Brain banks: benefits, limitations and cautions concerning the use of post-mortem brain tissue for molecular studies.

Ferrer I, Martinez A, Boluda S, Parchi P, Barrachina M. Ferrer I, et al. Cell Tissue Bank. 2008 Sep;9(3):181-94. doi: 10.1007/s10561-008-9077-0. Epub 2008 Jun 10. Cell Tissue Bank. 2008. PMID: 18543077 Review.

7

Generalized muscle pseudo-hypertrophy and stiffness associated with the myotilin Ser55Phe mutation: a novel myotilinopathy phenotype?

Gamez J, Armstrong J, Shatunov A, Selva-O'Callaghan A, Dominguez-Oronoz R, Ortega A, Goldfarb L, Ferrer I, Olivé M. Gamez J, et al. Among authors: ferrer i. J Neurol Sci. 2009 Feb 15;277(1-2):167-71. doi: 10.1016/j.jns.2008.10.019. Epub 2008 Nov 22. J Neurol Sci. 2009. PMID: 19027924 Free PMC article.

8

TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies.

Olivé M, Janué A, Moreno D, Gámez J, Torrejón-Escribano B, Ferrer I. Olivé M, et al. Among authors: ferrer i. J Neuropathol Exp Neurol. 2009 Mar;68(3):262-73. doi: 10.1097/NEN.0b013e3181996d8f. J Neuropathol Exp Neurol. 2009. PMID: 19225410

9

Clinical, neuropathologic, and biochemical profile of the amyloid precursor protein I716F mutation.

Guardia-Laguarta C, Pera M, Clarimón J, Molinuevo JL, Sánchez-Valle R, Lladó A, Coma M, Gómez-Isla T, Blesa R, Ferrer I, Lleó A. Guardia-Laguarta C, et al. Among authors: ferrer i. J Neuropathol Exp Neurol. 2010 Jan;69(1):53-9. doi: 10.1097/NEN.0b013e3181c6b84d. J Neuropathol Exp Neurol. 2010. PMID: 20010303

10

"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

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