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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.
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.
Proximal limb weakness and amyotrophy in a man with silicosis.
Souza PVS, Bortholin T, Naylor FGM, Pinto WBVR, Schmidt B, Oliveira ASB. Souza PVS, et al. Among authors: bortholin t. Arq Neuropsiquiatr. 2018 Jan;76(1):59. doi: 10.1590/0004-282X20170175. Arq Neuropsiquiatr. 2018. PMID: 29364397 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
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.
24 results