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Risk factors and future directions for preventing and diagnosing exertional rhabdomyolysis.
Carneiro A, Viana-Gomes D, Macedo-da-Silva J, Lima GHO, Mitri S, Alves SR, Kolliari-Turner A, Zanoteli E, Neto FRA, Palmisano G, Pesquero JB, Moreira JC, Pereira MD. Carneiro A, et al. Among authors: zanoteli e. Neuromuscul Disord. 2021 Jul;31(7):583-595. doi: 10.1016/j.nmd.2021.04.007. Epub 2021 May 6. Neuromuscul Disord. 2021. PMID: 34193371 Review.
Clinical Manifestation of Nebulin-Associated Nemaline Myopathy.
Moreno CAM, Artilheiro MC, Fonseca ATQSM, Camelo CG, de Medeiros GC, Sassi FC, de Andrade CRF, Donkervoort S, Silva AMS, Dalfior-Junior L, Abath-Neto OL, Reed UC, Bönnemann C, Zanoteli E. Moreno CAM, et al. Among authors: zanoteli e. Neurol Genet. 2023 Jan 25;9(1):e200056. doi: 10.1212/NXG.0000000000200056. eCollection 2023 Feb. Neurol Genet. 2023. PMID: 36714460 Free PMC article.
Longitudinal data collection in pediatric and adult patients with 5q spinal muscular atrophy in Latin America: LATAM RegistrAME study - a clinical registry study protocol.
Batista EC, Zanoteli E, Monfardini F, Santos GPD, Silva GS, Berwanger O, Rizzo LV, Fonseca HARD. Batista EC, et al. Among authors: zanoteli e. Einstein (Sao Paulo). 2024 Dec 9;22:eAE1133. doi: 10.31744/einstein_journal/2024AE1133. eCollection 2024. Einstein (Sao Paulo). 2024. PMID: 39661851 Free PMC article.
A new mutation in PYGM causing McArdle disease in a Brazilian patient.
Gomes CP, da Silva AMS, Zanoteli E, Pesquero JB. Gomes CP, et al. Among authors: zanoteli e. Acta Neurol Belg. 2020 Jun;120(3):705-707. doi: 10.1007/s13760-019-01159-7. Epub 2019 Jun 7. Acta Neurol Belg. 2020. PMID: 31175620 No abstract available.
Rhabdomyolysis: a genetic perspective.
Scalco RS, Gardiner AR, Pitceathly RD, Zanoteli E, Becker J, Holton JL, Houlden H, Jungbluth H, Quinlivan R. Scalco RS, et al. Among authors: zanoteli e. Orphanet J Rare Dis. 2015 May 2;10:51. doi: 10.1186/s13023-015-0264-3. Orphanet J Rare Dis. 2015. PMID: 25929793 Free PMC article. Review.
166 results