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ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
Montecchiani C, Pedace L, Lo Giudice T, Casella A, Mearini M, Gaudiello F, Pedroso JL, Terracciano C, Caltagirone C, Massa R, St George-Hyslop PH, Barsottini OG, Kawarai T, Orlacchio A. Montecchiani C, et al. Among authors: barsottini og. Brain. 2016 Jan;139(Pt 1):73-85. doi: 10.1093/brain/awv320. Epub 2015 Nov 10. Brain. 2016. PMID: 26556829 Free PMC article.
Clinical correlates of olfactory dysfunction in spinocerebellar ataxia type 3.
Braga-Neto P, Felicio AC, Pedroso JL, Dutra LA, Bertolucci PH, Gabbai AA, Barsottini OG. Braga-Neto P, et al. Among authors: barsottini og. Parkinsonism Relat Disord. 2011 Jun;17(5):353-6. doi: 10.1016/j.parkreldis.2011.02.004. Epub 2011 Mar 1. Parkinsonism Relat Disord. 2011. PMID: 21367642
Teaching NeuroImages: brucellosis mimicking demyelinating disease.
Abrahão A, de Aquino CC, Pedroso JL, Baiense RF, Oliveira RA, Jorge VM, Barsottini OG. Abrahão A, et al. Among authors: barsottini og. Neurology. 2011 Mar 15;76(11):e51. doi: 10.1212/WNL.0b013e3182104370. Neurology. 2011. PMID: 21403104 No abstract available.
Sleep disorders in cerebellar ataxias.
Pedroso JL, Braga-Neto P, Felício AC, Aquino CC, Prado LB, Prado GF, Barsottini OG. Pedroso JL, et al. Among authors: barsottini og. Arq Neuropsiquiatr. 2011 Apr;69(2A):253-7. doi: 10.1590/s0004-282x2011000200021. Arq Neuropsiquiatr. 2011. PMID: 21537570 Free article. Review.
305 results