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Arq Neuropsiquiatr. 2019 Sep 5;77(8):598. doi: 10.1590/0004-282X20190102.
Arq Neuropsiquiatr. 2019.
PMID: 31508690
Free article.
No abstract available.
Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias.
Giordani GM, Diniz F, Fussiger H, Gonzalez-Salazar C, Donis KC, Freua F, Ortega RPM, de Freitas JL, Barsottini OGP, Rosemberg S, Kok F, Pedroso JL, França MC Jr, Saute JAM.
Giordani GM, et al. Among authors: ortega rpm.
Sci Rep. 2021 Nov 15;11(1):22248. doi: 10.1038/s41598-021-01635-2.
Sci Rep. 2021.
PMID: 34782662
Free PMC article.
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Hereditary spastic paraplegia: a clinical and epidemiological study of a Brazilian pediatric population.
Ortega RPM, Rosemberg S.
Ortega RPM, et al.
Arq Neuropsiquiatr. 2019 Jan;77(1):10-18. doi: 10.1590/0004-282X20180153.
Arq Neuropsiquiatr. 2019.
PMID: 30758437
Free article.
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A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome.
Estephan EP, Sobreira CFDR, Dos Santos ACJ, Tomaselli PJ, Marques W Jr, Ortega RPM, Costa MCM, da Silva AMS, Mendonça RH, Caldas VM, Zambon AA, Abath Neto O, Marchiori PE, Heise CO, Reed UC, Azuma Y, Töpf A, Lochmüller H, Zanoteli E.
Estephan EP, et al. Among authors: ortega rpm.
J Neurol. 2018 Mar;265(3):708-713. doi: 10.1007/s00415-018-8736-8. Epub 2018 Jan 30.
J Neurol. 2018.
PMID: 29383513
Free PMC article.
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