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Myasthenia gravis in clinical practice.
Estephan EP, Baima JPS, Zambon AA. Estephan EP, et al. Arq Neuropsiquiatr. 2022 May;80(5 Suppl 1):257-265. doi: 10.1590/0004-282X-ANP-2022-S105. Arq Neuropsiquiatr. 2022. PMID: 35976295 Free PMC article. Review.
The Location of Disease-Causing DES Variants Determines the Severity of Phenotype and the Morphology of Sarcoplasmic Aggregates.
Silva AMS, Rodrigo P, Moreno CAM, Mendonça RH, Estephan EP, Camelo CG, Campos ED, Dias AT, Nascimento AM, Kulikowski LD, Oliveira ASB, Reed UC, Goldfarb LG, Olivé M, Zanoteli E. Silva AMS, et al. Among authors: estephan ep. J Neuropathol Exp Neurol. 2022 Aug 16;81(9):746-757. doi: 10.1093/jnen/nlac063. J Neuropathol Exp Neurol. 2022. PMID: 35898174
Effect of the COVID-19 pandemic on patients with inherited neuromuscular disorders.
Moreno CAM, Camelo CG, Sampaio PHMA, Fonseca ATQSM, Estephan EP, Silva AMS, Pirola RN, Silva LHL, Lima KDF, Albuquerque MAV, Camelo Filho AE, Marques MVO, Yanagiura MT, Cavalcante WCP, Matsui Junior C, Isihi LMA, Mendonça RH, Pouza AFP, Carvalho MS, Reed UC, Zanoteli E. Moreno CAM, et al. Among authors: estephan ep. Arq Neuropsiquiatr. 2022 Jun;80(6):563-569. doi: 10.1590/0004-282X-ANP-2021-0166. Arq Neuropsiquiatr. 2022. PMID: 35946707 Free PMC article.
The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.
Rodríguez Cruz PM, Cossins J, Estephan EP, Munell F, Selby K, Hirano M, Maroofin R, Mehrjardi MYV, Chow G, Carr A, Manzur A, Robb S, Munot P, Wei Liu W, Banka S, Fraser H, De Goede C, Zanoteli E, Conti Reed U, Sage A, Gratacos M, Macaya A, Dusl M, Senderek J, Töpf A, Hofer M, Knight R, Ramdas S, Jayawant S, Lochmüller H, Palace J, Beeson D. Rodríguez Cruz PM, et al. Among authors: estephan ep. Brain. 2019 Jun 1;142(6):1547-1560. doi: 10.1093/brain/awz107. Brain. 2019. PMID: 31081514 Free PMC article.
18 results