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Does ALS-FUS without FUS mutation represent ALS-FET? Report of three cases.
Borrego-Écija S, Cortés-Vicente E, Cervera-Carles L, Clarimón J, Gámez J, Batlle J, Ricken G, Molina-Porcel L, Aldecoa I, Sánchez-Valle R, Rojas-García R, Gelpi E. Borrego-Écija S, et al. Neuropathol Appl Neurobiol. 2019 Jun;45(4):421-426. doi: 10.1111/nan.12527. Epub 2018 Nov 20. Neuropathol Appl Neurobiol. 2019. PMID: 30375034 No abstract available.
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. 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.
A novel exon 3 mutation (D76V) in the SOD1 gene associated with slowly progressive ALS.
Segovia-Silvestre T, Andreu AL, Vives-Bauza C, Garcia-Arumi E, Cervera C, Gamez J. Segovia-Silvestre T, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Jun;3(2):69-74. doi: 10.1080/146608202760196039. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002. PMID: 12215228
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