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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2019 | 2 |
2020 | 1 |
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2023 | 1 |
2024 | 0 |
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Page 1
Update of the Brazilian consensus recommendations on Duchenne muscular dystrophy.
Arq Neuropsiquiatr. 2023 Jan;81(1):81-94. doi: 10.1055/s-0043-1761466. Epub 2023 Mar 14.
Arq Neuropsiquiatr. 2023.
PMID: 36918011
Free PMC article.
Review.
Characterisation of ataxia in Sjogren's syndrome.
Jaques CS, de Moraes MPM, Silva EAR, Coimbra-Neto AR, Martinez ARM, Camargos ST, Cardoso F, França MC, Nucci A, Pedroso JL, Barsottini OGP.
Jaques CS, et al. Among authors: coimbra neto ar.
J Neurol Neurosurg Psychiatry. 2020 Apr;91(4):446-448. doi: 10.1136/jnnp-2019-322373. Epub 2020 Feb 3.
J Neurol Neurosurg Psychiatry. 2020.
PMID: 32015088
No abstract available.
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A Novel Multisystem Proteinopathy Caused by a Missense ANXA11 Variant.
Leoni TB, González-Salazar C, Rezende TJR, Hernández ALC, Mattos AHB, Coimbra Neto AR, da Graça FF, Gonçalves JPN, Martinez ARM, Taniguti L, Kitajima JP, Kok F, Rogério F, da Silva AMS, de Oliveira ALR, Zanoteli E, Nucci A, França MC Jr.
Leoni TB, et al. Among authors: coimbra neto ar.
Ann Neurol. 2021 Aug;90(2):239-252. doi: 10.1002/ana.26136. Epub 2021 Jun 14.
Ann Neurol. 2021.
PMID: 34048612
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Intrafamilial phenotypic heterogeneity related to a new DMD splice site variant.
Coimbra Neto AR, de Carvalho SC, Leoni TB, Iwabe C, Silva TQAC, Coelho-Filho OR, Marques MJ, Nucci A, França MC Jr.
Coimbra Neto AR, et al.
Neuromuscul Disord. 2021 Aug;31(8):788-797. doi: 10.1016/j.nmd.2021.05.013. Epub 2021 Jun 2.
Neuromuscul Disord. 2021.
PMID: 34312044
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Clinical and molecular findings in a cohort of ANO5-related myopathy.
Silva AMS, Coimbra-Neto AR, Souza PVS, Winckler PB, Gonçalves MVM, Cavalcanti EBU, Carvalho AADS, Sobreira CFDR, Camelo CG, Mendonça RDH, Estephan EDP, Reed UC, Machado-Costa MC, Dourado-Junior MET, Pereira VC, Cruzeiro MM, Helito PVP, Aivazoglou LU, Camargo LVD, Gomes HH, Camargo AJSD, Pinto WBVDR, Badia BML, Libardi LH, Yanagiura MT, Oliveira ASB, Nucci A, Saute JAM, França-Junior MC, Zanoteli E.
Silva AMS, et al. Among authors: coimbra neto ar.
Ann Clin Transl Neurol. 2019 Jul;6(7):1225-1238. doi: 10.1002/acn3.50801. Epub 2019 Jun 11.
Ann Clin Transl Neurol. 2019.
PMID: 31353849
Free PMC article.
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Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy.
Winckler PB, da Silva AMS, Coimbra-Neto AR, Carvalho E, Cavalcanti EBU, Sobreira CFR, Marrone CD, Machado-Costa MC, Carvalho AAS, Feio RHF, Rodrigues CL, Gonçalves MVM, Tenório RB, Mendonça RH, Cotta A, Paim JFO, Costa E Silva C, de Aquino Cruz C, Bená MI, Betancur DFA, El Husny AS, de Souza ICN, Duarte RCB, Reed UC, Chaves MLF, Zanoteli E, França MC Jr, Saute JA.
Winckler PB, et al. Among authors: coimbra neto ar.
Clin Genet. 2019 Oct;96(4):341-353. doi: 10.1111/cge.13597. Epub 2019 Jul 15.
Clin Genet. 2019.
PMID: 31268554
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Male systemic lupus erythematosus, an overlooked diagnosis.
do Socorro Teixeira Moreira Almeida M, da Costa Arcoverde J, Barros Jacobino MN, Coimbra Neto AR.
do Socorro Teixeira Moreira Almeida M, et al. Among authors: coimbra neto ar.
Clin Pract. 2011 Nov 8;1(4):e103. doi: 10.4081/cp.2011.e103. eCollection 2011 Sep 28.
Clin Pract. 2011.
PMID: 24765344
Free PMC article.
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