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Page 1
Intraventricular Neurocysticercosis: The Role of Advanced MRI Sequences.
Guedes BF, Freua F, Parmera JB, Milano BG, Comerlatti LR, Silva GD, Lucato LT. Guedes BF, et al. Among authors: freua f. Neurol India. 2020 May-Jun;68(3):716-717. doi: 10.4103/0028-3886.288999. Neurol India. 2020. PMID: 32643702 Free article. No abstract available.
A novel GFAP mutation in a type II (late-onset) Alexander disease patient.
de Paiva AR, Freua F, Lucato LT, Parmera J, Dória D, Nóbrega PR, Olávio TR, Macedo-Souza LI, Kok F. de Paiva AR, et al. Among authors: freua f. J Neurol. 2016 Apr;263(4):821-2. doi: 10.1007/s00415-016-8065-8. Epub 2016 Feb 25. J Neurol. 2016. PMID: 26914930 No abstract available.
Susac syndrome.
Freua F, Lucato LT, Villela F, Rabello GD. Freua F, et al. Arq Neuropsiquiatr. 2014 Oct;72(10):812-3. doi: 10.1590/0004-282x20140128. Arq Neuropsiquiatr. 2014. PMID: 25337735 Free article. No abstract available.
Chronic stage of Marchiafava-Bignami disease.
Lucato LT, Freua F, Kok F. Lucato LT, et al. Among authors: freua f. Arq Neuropsiquiatr. 2015 Oct;73(10):890. doi: 10.1590/0004-282X20150103. Epub 2015 Aug 11. Arq Neuropsiquiatr. 2015. PMID: 26291992 Free article. No abstract available.
PUS3 mutations are associated with intellectual disability, leukoencephalopathy, and nephropathy.
de Paiva ARB, Lynch DS, Melo US, Lucato LT, Freua F, de Assis BDR, Barcelos I, Listik C, de Castro Dos Santos D, Macedo-Souza LI, Houlden H, Kok F. de Paiva ARB, et al. Among authors: freua f. Neurol Genet. 2019 Jan 16;5(1):e306. doi: 10.1212/NXG.0000000000000306. eCollection 2019 Feb. Neurol Genet. 2019. PMID: 30697592 Free PMC article. No abstract available.
Typical clinical and neuroimaging features in Sjögren-Larsson syndrome.
Paiva ARB, Melo US, Freua F, Dória D, Cabral KSS, Macedo-Souza LI, Lucato LT, Kok F. Paiva ARB, et al. Among authors: freua f. Arq Neuropsiquiatr. 2018 Apr;76(4):283. doi: 10.1590/0004-282x20180024. Arq Neuropsiquiatr. 2018. PMID: 29742247 Free article. No abstract available.
A novel complex neurological phenotype due to a homozygous mutation in FDX2.
Gurgel-Giannetti J, Lynch DS, Paiva ARB, Lucato LT, Yamamoto G, Thomsen C, Basu S, Freua F, Giannetti AV, de Assis BDR, Ribeiro MDO, Barcelos I, Sayão Souza K, Monti F, Melo US, Amorim S, Silva LGL, Macedo-Souza LI, Vianna-Morgante AM, Hirano M, Van der Knaap MS, Lill R, Vainzof M, Oldfors A, Houlden H, Kok F. Gurgel-Giannetti J, et al. Among authors: freua f. Brain. 2018 Aug 1;141(8):2289-2298. doi: 10.1093/brain/awy172. Brain. 2018. PMID: 30010796 Free PMC article.
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