de Souza PVS - Search Results

1

Editorial: The expanding clinical and genetic basis of adult inherited neurometabolic disorders.

Pinto WBVR, Oliveira ASB, Carvalho AAS, Akman HO, de Souza PVS. Pinto WBVR, et al. Among authors: de souza pvs. Front Neurol. 2023 Jul 25;14:1255513. doi: 10.3389/fneur.2023.1255513. eCollection 2023. Front Neurol. 2023. PMID: 37560451 Free PMC article. No abstract available.

2

Phelan-McDermid syndrome presenting with autistic spectrum: are we underdiagnosing chromosomal diseases in patients with autism?

de Rezende Pinto WB, Pedroso JL, de Souza PV, Oliveira AS, Barsottini OG. de Rezende Pinto WB, et al. J Neurol. 2013 Sep 29. doi: 10.1007/s00415-013-7127-4. Online ahead of print. J Neurol. 2013. PMID: 24078047 No abstract available.

3

DARS2 gene clinical spectrum: new ideas regarding an underdiagnosed leukoencephalopathy.

Pinto WB, de Souza PV. Pinto WB, et al. Brain. 2014 Jul;137(Pt 7):e289. doi: 10.1093/brain/awu134. Epub 2014 May 24. Brain. 2014. PMID: 24860140 Free article. No abstract available.

4

Ossifying fibroma of the maxilla and tuberous sclerosis complex.

Pinto WB, de Souza PV, dos Santos AJ. Pinto WB, et al. Neurology. 2015 Apr 14;84(15):1611-2. doi: 10.1212/WNL.0000000000001478. Neurology. 2015. PMID: 25870452 No abstract available.

5

Retinitis pigmentosa in Lafora disease: expanding findings of progressive myoclonic epilepsy.

Pinto WB, de Souza PV, Pinheiro JR, Okamoto KY, Enokihara MM, Oliveira AS. Pinto WB, et al. Neurology. 2015 Sep 22;85(12):1087. doi: 10.1212/WNL.0000000000001957. Neurology. 2015. PMID: 26391413 No abstract available.

6

Teaching NeuroImages: Leukodystrophy and progressive myoclonic epilepsy disclosing DRPLA.

de Souza PV, Batistella GN, Pinto WB, Oliveira AS. de Souza PV, et al. Neurology. 2016 Feb 9;86(6):e58-9. doi: 10.1212/WNL.0000000000002356. Neurology. 2016. PMID: 26857957 No abstract available.

7

Retinitis pigmentosa in Lafora disease: Expanding findings of progressive myoclonic epilepsy.

Carpenter S, de Rezende Pinto WB, de Souza PV, Oliveira AS. Carpenter S, et al. Neurology. 2016 Apr 19;86(16):1563. doi: 10.1212/WNL.0000000000002622. Neurology. 2016. PMID: 27164451 No abstract available.

8

Collagen type VI-related myopathy.

de Souza PVS, Bortholin T, Pinheiro JRS, Naylor FGM, Pinto WBVR, Oliveira ASB. de Souza PVS, et al. 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.

9

Familial progressive bilateral facial paralysis in Finnish type hereditary amyloidosis.

de Souza PVS, Bortholin T, Naylor FGM, Dias RB, Pinto WBVR, Oliveira ASB. de Souza PVS, et al. Pract Neurol. 2017 Oct;17(5):408-409. doi: 10.1136/practneurol-2017-001690. Epub 2017 Jun 3. Pract Neurol. 2017. PMID: 28578319 No abstract available.

10

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. Among authors: de souza pvs. Neurology. 2021 Mar 30;96(13):627-628. doi: 10.1212/WNL.0000000000011663. Epub 2021 Feb 10. Neurology. 2021. PMID: 33568539 No abstract available.

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