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Inflammatory myopathies: an update for neurologists.
Silva AMS, Campos ED, Zanoteli E. Silva AMS, et al. Arq Neuropsiquiatr. 2022 May;80(5 Suppl 1):238-248. doi: 10.1590/0004-282X-ANP-2022-S131. Arq Neuropsiquiatr. 2022. PMID: 35976321 Free PMC article. Review.
Facial myokymia in inherited peripheral nerve hyperexcitability syndrome.
Camelo CG, Silva AMS, Moreno CAM, Matsui-Júnior C, Heise CO, Pedroso JL, Zanoteli E. Camelo CG, et al. Among authors: silva ams. Pract Neurol. 2020 May;20(3):253-255. doi: 10.1136/practneurol-2019-002462. Epub 2020 Mar 17. Pract Neurol. 2020. PMID: 32184343
Neurological consultations and diagnoses in a large, dedicated COVID-19 university hospital.
Studart-Neto A, Guedes BF, Tuma RLE, Camelo Filho AE, Kubota GT, Iepsen BD, Moreira GP, Rodrigues JC, Ferrari MMH, Carra RB, Spera RR, Oku MHM, Terrim S, Lopes CCB, Passos Neto CEB, Fiorentino MD, DE Souza JCC, Baima JPS, DA Silva TFF, Moreno CAM, Silva AMS, Heise CO, MendonÇa RH, Fortini I, Smid J, Adoni T, GonÇalves MRR, Pereira SLA, Pinto LF, Gomes HR, Zanoteli E, Brucki SMD, Conforto AB, Castro LHM, Nitrini R. Studart-Neto A, et al. Among authors: silva ams. Arq Neuropsiquiatr. 2020 Aug 3;78(8):494-500. doi: 10.1590/0004-282x20200089. Arq Neuropsiquiatr. 2020. PMID: 32756734 Free article.
Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy.
Mendonça RH, Matsui C Jr, Polido GJ, Silva AMS, Kulikowski L, Torchio Dias A, Zanardo EA, Solla DJF, Gurgel-Giannetti J, de Moura ACML, Sampaio GPC, Oliveira ASB, de Souza PVS, Pinto WBVR, Gonçalves EA, Farias IB, Nardes F, Araújo APQC, Marques W Jr, Tomaselli PJ, Ribeiro MDO, Kitajima JP, Paoli Monteiro F, Saute JAM, Becker MM, Saraiva-Pereira ML, Brusius-Facchin AC, van der Linden V, Florêncio RN, Barbosa AVS, Machado-Costa MC, Pessoa ALS, Souza LS, Franca MC Jr, Kok F, Reed UC, Zanoteli E. Mendonça RH, et al. Among authors: silva ams. Neurol Genet. 2020 Sep 1;6(5):e505. doi: 10.1212/NXG.0000000000000505. eCollection 2020 Oct. Neurol Genet. 2020. PMID: 33062891 Free PMC article.
Severe progressive brain involvement in a patient with TRMT10C mutation.
Camelo CG, Silva AMS, Rocha AJ, Scaramuzzi V, Moreno CAM, Reed UC, Zanoteli E. Camelo CG, et al. Among authors: silva ams. Arq Neuropsiquiatr. 2021 Mar;79(3):259-260. doi: 10.1590/0004-282X-ANP-2020-0355. Arq Neuropsiquiatr. 2021. PMID: 33886802 Free article. No abstract available.
416 results