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Page 1
Progression rate of myelopathy in X-linked adrenoleukodystrophy heterozygotes.
Habekost CT, Pereira FS, Vargas CR, Coelho DM, Torrez V, Oses JP, Portela LV, Schestatsky P, Felix VT, Matte U, Torman VL, Jardim LB. Habekost CT, et al. Metab Brain Dis. 2015 Oct;30(5):1279-84. doi: 10.1007/s11011-015-9672-2. Epub 2015 Apr 30. Metab Brain Dis. 2015. PMID: 25920484
Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors.
Monte TL, Pereira FS, Reckziegel EDR, Augustin MC, Locks-Coelho LD, Santos ASP, Pedroso JL, Barsottini O, Vargas FR, Saraiva-Pereira ML, Jardim LB; Rede Neurogenética. Monte TL, et al. Parkinsonism Relat Disord. 2017 Sep;42:54-60. doi: 10.1016/j.parkreldis.2017.06.010. Epub 2017 Jun 19. Parkinsonism Relat Disord. 2017. PMID: 28648514
ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America.
Pereira FS, Monte TL, Locks-Coelho LD, Silva AS, Barsottini O, Pedroso JL, Cornejo-Olivas M, Mazzetti P, Godeiro C, Vargas FR, Lima MA, van der Linden H Jr, Toralles MB, Medeiros PF, Ribeiro E, Braga-Neto P, Salarini D, Castilhos RM, Saraiva-Pereira ML, Jardim LB; Rede Neurogenetica. Pereira FS, et al. Cerebellum. 2015 Dec;14(6):728-30. doi: 10.1007/s12311-015-0666-8. Cerebellum. 2015. PMID: 25869926 No abstract available.
12 results