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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 2
2009 2
2010 3
2014 1
2015 1
2016 1
2017 3
2018 3
2019 5
2020 1
2021 2
2022 0
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20 results
Results by year
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Page 1
Atypical Motor Neuron Disease variants: Still a diagnostic challenge in Neurology.
Pinto WBVR, Debona R, Nunes PP, Assis ACD, Lopes CG, Bortholin T, Dias RB, Naylor FGM, Chieia MAT, Souza PVS, Oliveira ASB. Pinto WBVR, et al. Among authors: chieia mat. Rev Neurol (Paris). 2019 Apr;175(4):221-232. doi: 10.1016/j.neurol.2018.04.016. Epub 2019 Mar 4. Rev Neurol (Paris). 2019. PMID: 30846210 Review.
Motor neuron disease in inherited neurometabolic disorders.
de Souza PVS, Bortholin T, Naylor FGM, Chieia MAT, de Rezende Pinto WBV, Oliveira ASB. de Souza PVS, et al. Among authors: chieia mat. Rev Neurol (Paris). 2018 Mar;174(3):115-124. doi: 10.1016/j.neurol.2017.06.020. Epub 2017 Nov 8. Rev Neurol (Paris). 2018. PMID: 29128155 Review.
Clinical and genetic basis of familial amyotrophic lateral sclerosis.
Souza PV, Pinto WB, Chieia MA, Oliveira AS. Souza PV, et al. Among authors: chieia ma. Arq Neuropsiquiatr. 2015 Dec;73(12):1026-37. doi: 10.1590/0004-282X20150161. Epub 2015 Oct 13. Arq Neuropsiquiatr. 2015. PMID: 26465287 Free article. Review.
Clinical and radiological profile of patients with spinal muscular atrophy type 4.
Souza PVS, Pinto WBVR, Ricarte A, Badia BML, Seneor DD, Teixeira DT, Caetano L, Gonçalves EA, Chieia MAT, Farias IB, Bertini E, Oliveira ASB. Souza PVS, et al. Among authors: chieia mat. Eur J Neurol. 2021 Feb;28(2):609-619. doi: 10.1111/ene.14587. Epub 2020 Nov 12. Eur J Neurol. 2021. PMID: 33090613
Progressive spastic tetraplegia and axial hypotonia (STAHP) due to SOD1 deficiency: is it really a new entity?
de Souza PVS, Pinto WBVR, Farias IB, Badia BML, Pinto IFN, Costa GC, Marin CM, Dos Santos Jorge AC, Souto EC, Serrano PL, Machado RIL, Chieia MAT, Bertini E, Oliveira ASB. de Souza PVS, et al. Among authors: chieia mat. Orphanet J Rare Dis. 2021 Aug 11;16(1):360. doi: 10.1186/s13023-021-01993-0. Orphanet J Rare Dis. 2021. PMID: 34380534 Free PMC article.
Pseudoxanthoma elasticum presenting as akinetic-rigid parkinsonism and dementia.
Souza PVS, Badia BML, Pinto WBVR, Oliveira ASB, Silva LHL, Seneor DD, Marin VDGB, Teixeira Júnior CAC, Chieia MAT, Farias IB. Souza PVS, et al. Among authors: chieia mat. Arq Neuropsiquiatr. 2019 Jul 29;77(7):525-526. doi: 10.1590/0004-282X20190075. Arq Neuropsiquiatr. 2019. PMID: 31365645 Free article. No abstract available.
O'Sullivan-McLeod syndrome: Unmasking a rare atypical motor neuron disease.
Pinto WBVR, Nunes PP, Lima E Teixeira I, Assis ACD, Naylor FGM, Chieia MAT, Souza PVS, A S B Oliveira. Pinto WBVR, et al. Among authors: chieia mat. Rev Neurol (Paris). 2019 Jan-Feb;175(1-2):81-86. doi: 10.1016/j.neurol.2018.04.009. Epub 2018 Nov 5. Rev Neurol (Paris). 2019. PMID: 30409480
New genetic causes for complex hereditary spastic paraplegia.
Souza PVS, Bortholin T, Dias RB, Chieia MAT, Burlin S, Naylor FGM, Pinto WBVR, Oliveira ASB. Souza PVS, et al. Among authors: chieia mat. J Neurol Sci. 2017 Aug 15;379:283-292. doi: 10.1016/j.jns.2017.06.019. Epub 2017 Jun 15. J Neurol Sci. 2017. PMID: 28716262
20 results