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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.
Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations.
Melo US, Freua F, Lynch DS, Ripa BD, Tenorio RB, Saute JAM, de Souza Leite F, Kitajima J, Houlden H, Zatz M, Kok F. Melo US, et al. Among authors: freua f. Clin Genet. 2018 Nov;94(5):482-483. doi: 10.1111/cge.13428. Epub 2018 Sep 10. Clin Genet. 2018. PMID: 30198554 No abstract available.
Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.
Freua F, Almeida MEC, Nóbrega PR, Paiva ARB, Della-Ripa B, Cunha P, Macedo-Souza LI, Bueno C, Lynch DS, Houlden H, Lucato LT, Kok F. Freua F, et al. Cold Spring Harb Mol Case Stud. 2022 Sep 30;8(6):a006232. doi: 10.1101/mcs.a006232. Online ahead of print. Cold Spring Harb Mol Case Stud. 2022. PMID: 36180229 Free PMC article.
SCA23 and prodynorphin: is it time for gene retraction?
Pedroso JL, Vale TC, Freua F, Barsottini OG, Kok F. Pedroso JL, et al. Among authors: freua f. Brain. 2016 Aug;139(Pt 8):e42. doi: 10.1093/brain/aww093. Epub 2016 May 1. Brain. 2016. PMID: 27190015 No abstract available.
Clinical and genetic characterization of leukoencephalopathies in adults.
Lynch DS, Rodrigues Brandão de Paiva A, Zhang WJ, Bugiardini E, Freua F, Tavares Lucato L, Macedo-Souza LI, Lakshmanan R, Kinsella JA, Merwick A, Rossor AM, Bajaj N, Herron B, McMonagle P, Morrison PJ, Hughes D, Pittman A, Laurà M, Reilly MM, Warren JD, Mummery CJ, Schott JM, Adams M, Fox NC, Murphy E, Davagnanam I, Kok F, Chataway J, Houlden H. Lynch DS, et al. Among authors: freua f. Brain. 2017 May 1;140(5):1204-1211. doi: 10.1093/brain/awx045. Brain. 2017. PMID: 28334938 Free PMC article.
28 results