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Single-centre experience with autosomal recessive limb-girdle muscular dystrophy: case series and literature review.
Arq Neuropsiquiatr. 2023 Oct;81(10):922-933. doi: 10.1055/s-0043-1772833. Epub 2023 Oct 18.
Arq Neuropsiquiatr. 2023.
PMID: 37852290
Free PMC article.
Review.
Congenital myasthenic syndrome in a cohort of patients with 'double' seronegative myasthenia gravis.
Lorenzoni PJ, Ducci RD, Arndt RC, Hrysay NMC, Fustes OJH, Töpf A, Lochmüller H, Werneck LC, Kay CSK, Scola RH.
Lorenzoni PJ, et al. Among authors: hrysay nmc.
Arq Neuropsiquiatr. 2022 Jan;80(1):69-74. doi: 10.1590/0004-282X-ANP-2020-0575.
Arq Neuropsiquiatr. 2022.
PMID: 34932651
Free PMC article.
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Genomics and Virulence of Fonsecaea pugnacius, Agent of Disseminated Chromoblastomycosis.
Bombassaro A, Schneider GX, Costa FF, Leão ACR, Soley BS, Medeiros F, da Silva NM, Lima BJFS, Castro RJA, Bocca AL, Baura VA, Balsanelli E, Pankievicz VCS, Hrysay NMC, Scola RH, Moreno LF, Azevedo CMPS, Souza EM, Gomes RR, de Hoog S, Vicente VA.
Bombassaro A, et al. Among authors: hrysay nmc.
Front Genet. 2020 Aug 4;11:822. doi: 10.3389/fgene.2020.00822. eCollection 2020.
Front Genet. 2020.
PMID: 32849816
Free PMC article.
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Congenital myasthenic syndrome due to DOK7 mutation in a cohort of patients with 'unexplained' limb-girdle muscular weakness.
Lorenzoni PJ, Kay CSK, Arndt RC, Hrysay NMC, Ducci RD, Fustes OHJ, Töpf A, Lochmüller H, Werneck LC, Scola RH.
Lorenzoni PJ, et al. Among authors: hrysay nmc.
J Clin Neurosci. 2020 May;75:195-198. doi: 10.1016/j.jocn.2020.01.080. Epub 2020 Mar 29.
J Clin Neurosci. 2020.
PMID: 32238315
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