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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: pesquero jb. 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.
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: pesquero jb. 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.
New mutations in the GLA gene in Brazilian families with Fabry disease.
Turaça LT, Pessoa JG, Motta FL, Muñoz Rojas MV, Müller KB, Lourenço CM, Junior Marques W, D'Almeida V, Martins AM, Pesquero JB. Turaça LT, et al. Among authors: pesquero jb. J Hum Genet. 2012 Jun;57(6):347-51. doi: 10.1038/jhg.2012.32. Epub 2012 May 3. J Hum Genet. 2012. PMID: 22551898
314 results