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Year Number of Results
2016 3
2017 15
2018 6
2019 2
2023 1
2024 0

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24 results

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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: bortholin t. 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.
Postictal thoracocervicofacial purpura.
de Souza PVS, Bortholin T, de Rezende Pinto WBV, Santos AJ. de Souza PVS, et al. Among authors: bortholin t. Pract Neurol. 2017 Aug;17(4):306. doi: 10.1136/practneurol-2017-001633. Epub 2017 Apr 20. Pract Neurol. 2017. PMID: 28428228 No abstract available.
Collagen type VI-related myopathy.
de Souza PVS, Bortholin T, Pinheiro JRS, Naylor FGM, Pinto WBVR, Oliveira ASB. de Souza PVS, et al. Among authors: bortholin t. Pract Neurol. 2017 Oct;17(5):406-407. doi: 10.1136/practneurol-2017-001661. Epub 2017 Jun 3. Pract Neurol. 2017. PMID: 28578317 No abstract available.
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: bortholin t. 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.
Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks.
de Souza PVS, de Rezende Pinto WBV, de Rezende Batistella GN, Bortholin T, Oliveira ASB. de Souza PVS, et al. Among authors: bortholin t. Cerebellum. 2017 Apr;16(2):525-551. doi: 10.1007/s12311-016-0803-z. Cerebellum. 2017. PMID: 27271711 Review.
Letter re: Acute intermittent porphyria-related leukoencephalopathy.
Pinto WB, Sgobbi de Souza PV, Bortholin T, Troccoli Chieia MA, Oliveira AS. Pinto WB, et al. Among authors: bortholin t. Neurology. 2017 Feb 14;88(7):718. doi: 10.1212/WNL.0000000000003624. Neurology. 2017. PMID: 28193753 No abstract available.
Perforating palmar disease in TTR-related familial amyloid polyneuropathy.
Souza PVS, Bortholin T, Teixeira CAC, Seneor DD, Marin VDGB, Naylor FGM, Pinto WBVR, Oliveira ASB. Souza PVS, et al. Among authors: bortholin t. Arq Neuropsiquiatr. 2018 Aug;76(8):569. doi: 10.1590/0004-282X20180066. Arq Neuropsiquiatr. 2018. PMID: 30231133 Free article. No abstract available.
Early-onset axonal Charcot-Marie-Tooth disease due to SACS mutation.
Souza PVS, Bortholin T, Naylor FGM, Pinto WBVR, Oliveira ASB. Souza PVS, et al. Among authors: bortholin t. Neuromuscul Disord. 2018 Feb;28(2):169-172. doi: 10.1016/j.nmd.2017.11.008. Epub 2017 Nov 24. Neuromuscul Disord. 2018. PMID: 29277257
24 results