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Genetic diversity in hereditary axonal neuropathy: Analyzing 53 Brazilian children.
J Peripher Nerv Syst. 2024 Mar;29(1):97-106. doi: 10.1111/jns.12617. Epub 2024 Feb 20.
J Peripher Nerv Syst. 2024.
PMID: 38375759
Update of the Brazilian consensus recommendations on Duchenne muscular dystrophy.
Araujo APQC, Saute JAM, Fortes CPDD, França MC Jr, Pereira JA, Albuquerque MAV, Carvalho AAS, Cavalcanti EBU, Covaleski APPM, Fagondes SC, Gurgel-Giannetti J, Gonçalves MVM, Martinez ARM, Coimbra Neto AR, Neves FR, Nucci A, Nucera APCDS, Pessoa ALS, Rebel MF, Santos FND, Scola RH, Sobreira CFDR.
Araujo APQC, et al. Among authors: covaleski appm.
Arq Neuropsiquiatr. 2023 Jan;81(1):81-94. doi: 10.1055/s-0043-1761466. Epub 2023 Mar 14.
Arq Neuropsiquiatr. 2023.
PMID: 36918011
Free PMC article.
Review.
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Allgrove syndrome with amyotrophy.
Soares MC, Lins OG, Lima de Carvalho JR, de Sá CC, Van der Linden V, Covaleski APPM.
Soares MC, et al. Among authors: covaleski appm.
Pract Neurol. 2022 Jun;22(3):213-215. doi: 10.1136/practneurol-2021-003192. Epub 2021 Dec 30.
Pract Neurol. 2022.
PMID: 34969826
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GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease.
Figueiredo FB, Silva WA Jr, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JE, Marques W Jr.
Figueiredo FB, et al. Among authors: covaleski appm.
Neuromuscul Disord. 2021 Jun;31(6):505-511. doi: 10.1016/j.nmd.2021.03.005. Epub 2021 Mar 20.
Neuromuscul Disord. 2021.
PMID: 33903021
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