Search Page

1

Cite

Share

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. 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.

Cite

Share

2

Cite

Share

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: pinto wbvr. 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.

Cite

Share

3

Cite

Share

Acute Hepatic Porphyria: Pathophysiological Basis of Neuromuscular Manifestations.

de Souza PVS, Badia BML, Farias IB, Pinto WBVR, Oliveira ASB. de Souza PVS, et al. Among authors: pinto wbvr. Front Neurosci. 2021 Sep 27;15:715523. doi: 10.3389/fnins.2021.715523. eCollection 2021. Front Neurosci. 2021. PMID: 34646118 Free PMC article. Review.

Cite

Share

4

Cite

Share

Adult-onset non-5q proximal spinal muscular atrophy: a comprehensive review.

Pinto WBVR, Souza PVS, Badia BML, Farias IB, Albuquerque Filho JMV, Gonçalves EA, Machado RIL, Oliveira ASB. Pinto WBVR, et al. Arq Neuropsiquiatr. 2021 Oct;79(10):912-923. doi: 10.1590/0004-282X-ANP-2020-0429. Arq Neuropsiquiatr. 2021. PMID: 34706022 Free article. Review.

Cite

Share

5

Cite

Share

GBE1-related disorders: Adult polyglucosan body disease and its neuromuscular phenotypes.

Souza PVS, Badia BML, Farias IB, Pinto WBVR, Oliveira ASB, Akman HO, DiMauro S. Souza PVS, et al. Among authors: pinto wbvr. J Inherit Metab Dis. 2021 May;44(3):534-543. doi: 10.1002/jimd.12325. Epub 2020 Nov 13. J Inherit Metab Dis. 2021. PMID: 33141444 Review.

Cite

Share

6

Cite

Share

Neuromuscular choristoma: a rare cause of congenital non-progressive lower limb amyotrophy.

Machado RIL, Alburquerque Filho JMV, Souza PVS, Aivazoglou LU, Badia BML, Ogata SYT, Farias IB, Aihara AY, Fernandes ADRC, Pinto WBVR, Oliveira ASB. Machado RIL, et al. Among authors: pinto wbvr. Arq Neuropsiquiatr. 2021 May;79(5):465-466. doi: 10.1590/0004-282X-ANP-2020-0370. Arq Neuropsiquiatr. 2021. PMID: 34037103 Free article. No abstract available.

Cite

Share

7

Cite

Share

Acute hepatic porphyrias for the neurologist: current concepts and perspectives.

Souza PVS, Badia BML, Farias IB, Gonçalves EA, Pinto WBVR, Oliveira ASB. Souza PVS, et al. Among authors: pinto wbvr. Arq Neuropsiquiatr. 2021 Jan;79(1):68-80. doi: 10.1590/0004-282X20200096. Arq Neuropsiquiatr. 2021. PMID: 33656101 Free article. Review.

Cite

Share

8

Cite

Share

Clinical and genetic basis of congenital myasthenic syndromes.

Souza PV, Batistella GN, Lino VC, Pinto WB, Annes M, Oliveira AS. Souza PV, et al. Among authors: pinto wb. Arq Neuropsiquiatr. 2016 Sep;74(9):750-760. doi: 10.1590/0004-282X20160106. Arq Neuropsiquiatr. 2016. PMID: 27706425 Free article. Review.

Cite

Share

9

Cite

Share

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy.

Pinto WBVR, Farias IB, Badia BML, Vieira de Albuquerque Filho JM, Machado RIL, de Souza PVS, Oliveira ASB. Pinto WBVR, et al. Neurology. 2021 Mar 30;96(13):627-628. doi: 10.1212/WNL.0000000000011663. Epub 2021 Feb 10. Neurology. 2021. PMID: 33568539 No abstract available.

Cite

Share

10

Cite

Share

Immune-mediated inflammatory polyneuropathy overlapping Charcot-Marie-Tooth 1B.

Escorcio-Bezerra ML, Pinto WBVR, Bichuetti DB, Souza PVS, Nunes RM, Silva LHL, Lima KDF, Manzano GM, Oliveira ASB, Baeta AM. Escorcio-Bezerra ML, et al. Among authors: pinto wbvr. J Clin Neurosci. 2020 May;75:228-231. doi: 10.1016/j.jocn.2020.03.014. Epub 2020 Mar 19. J Clin Neurosci. 2020. PMID: 32201027

Cite

Share