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2019 2
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2024 3

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14 results

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Page 1
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. 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.
Hypoglycemia in Patients With LAMA2-CMD.
Camelo CG, Martins Moreno CA, Artilheiro MC, Serafim Silva AM, Quadros Monteiro Fonseca AT, Mendonça de Holanda R, Reed UC, Zanoteli E. Camelo CG, et al. Pediatr Neurol. 2023 Jun;143:1-5. doi: 10.1016/j.pediatrneurol.2023.01.017. Epub 2023 Feb 7. Pediatr Neurol. 2023. PMID: 36934516
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: camelo cg. Neurol Genet. 2023 Jan 25;9(1):e200056. doi: 10.1212/NXG.0000000000200056. eCollection 2023 Feb. Neurol Genet. 2023. PMID: 36714460 Free PMC article.
European Joint Programme on Rare Diseases workshop: LAMA2-muscular dystrophy: paving the road to therapy March 17-19, 2023, Barcelona, Spain.
Smeets H, Verbrugge B, Bulbena X, Hristova L, Vogt J, van Beckhoven I; all participants; Patient organizations/patient representatives: LAMA2-Europe, Voor Sara-the Netherlands, ImpulsaT-Spain, LAMA2-France, CMD-Turkey, LAMA2-Bulgaria, Cure-CMD. Smeets H, et al. Neuromuscul Disord. 2024 Mar;36:16-22. doi: 10.1016/j.nmd.2024.01.001. Epub 2024 Jan 9. Neuromuscul Disord. 2024. PMID: 38306718
Genetic profile of Brazilian patients with LAMA2-related dystrophies.
Camelo CG, Moreno CAM, Artilheiro MDC, Fonseca ATQM, Gurgel Gianetti J, Barbosa AV, Donis KC, Saute JAM, Pessoa A, Van der Linden H Jr, Gonçalves ARA, Kulikowski LD, Kok F, Zanoteli E. Camelo CG, et al. Clin Genet. 2024 May 15. doi: 10.1111/cge.14538. Online ahead of print. Clin Genet. 2024. PMID: 38747280
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: camelo cg. Arq Neuropsiquiatr. 2022 Jun;80(6):563-569. doi: 10.1590/0004-282X-ANP-2021-0166. Arq Neuropsiquiatr. 2022. PMID: 35946707 Free PMC article.
Marked neuropsychiatric involvement and dysmorphic features in nemaline myopathy.
Nóbrega PR, de Brito de Souza JL, Maurício RB, de Paiva ARB, Dias DA, Camelo CG, Zanotelli E, Schlesinger D, Braga-Neto P, Moreno CAM. Nóbrega PR, et al. Among authors: camelo cg. Neurol Sci. 2024 Mar;45(3):1225-1231. doi: 10.1007/s10072-023-07128-6. Epub 2023 Oct 18. Neurol Sci. 2024. PMID: 37851294
Clinical features of collagen VI-related dystrophies: A large Brazilian cohort.
Zanoteli E, Soares PS, Silva AMSD, Camelo CG, Fonseca ATQSM, Albuquerque MAV, Moreno CAM, Lopes Abath Neto O, Novo Filho GM, Kulikowski LD, Reed UC. Zanoteli E, et al. Among authors: camelo cg. Clin Neurol Neurosurg. 2020 May;192:105734. doi: 10.1016/j.clineuro.2020.105734. Epub 2020 Feb 10. Clin Neurol Neurosurg. 2020. PMID: 32065942
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: camelo cg. J Neuropathol Exp Neurol. 2022 Aug 16;81(9):746-757. doi: 10.1093/jnen/nlac063. J Neuropathol Exp Neurol. 2022. PMID: 35898174
14 results