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Molecular imaging in hereditary forms of parkinsonism.
Shih MC, Felicio AC, de Oliveira Godeiro-Junior C, de Carvalho Aguiar P, de Andrade LA, Ferraz HB, Bressan RA. Shih MC, et al. Among authors: de carvalho aguiar p, de oliveira godeiro junior c, de andrade la. Eur J Neurol. 2007 Apr;14(4):359-68. doi: 10.1111/j.1468-1331.2007.01691.x. Eur J Neurol. 2007. PMID: 17388981 Review.
Heterozygous exon 3 deletion in the Parkin gene in a patient with clinical and radiological MSA-C phenotype.
Barsottini OG, Felício AC, de Carvalho Aguiar P, Godeiro-Junior C, Pedroso JL, de Aquino CC, Bor-Seng-Shu E, de Andrade LA. Barsottini OG, et al. Among authors: de carvalho aguiar p, de andrade la, de aquino cc. Clin Neurol Neurosurg. 2011 Jun;113(5):404-6. doi: 10.1016/j.clineuro.2010.11.015. Epub 2010 Dec 22. Clin Neurol Neurosurg. 2011. PMID: 21183274 No abstract available.
Novel THAP1 variants in Brazilian patients with idiopathic isolated dystonia.
da Silva-Junior FP, dos Santos CO, Silva SM, Barbosa ER, Borges V, Ferraz HB, Limongi JC, Rocha MS, de Carvalho Aguiar P. da Silva-Junior FP, et al. Among authors: de carvalho aguiar p. J Neurol Sci. 2014 Sep 15;344(1-2):190-2. doi: 10.1016/j.jns.2014.06.012. Epub 2014 Jun 17. J Neurol Sci. 2014. PMID: 24976531
Screening of GNAL variants in Brazilian patients with isolated dystonia reveals a novel mutation with partial loss of function.
Dos Santos CO, Masuho I, da Silva-Júnior FP, Barbosa ER, Silva SM, Borges V, Ferraz HB, Rocha MS, Limongi JC, Martemyanov KA, de Carvalho Aguiar P. Dos Santos CO, et al. Among authors: de carvalho aguiar p. J Neurol. 2016 Apr;263(4):665-8. doi: 10.1007/s00415-016-8026-2. Epub 2016 Jan 25. J Neurol. 2016. PMID: 26810727 Free PMC article.
37 results