Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

16 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease.
Pedroso JL, Rocha CR, Macedo-Souza LI, De Mario V, Marques W Jr, Barsottini OG, Bulle Oliveira AS, Menck CF, Kok F. Pedroso JL, et al. Among authors: bulle oliveira as. Neurol Genet. 2015 Oct 22;1(4):e30. doi: 10.1212/NXG.0000000000000030. eCollection 2015 Dec. Neurol Genet. 2015. PMID: 27066567 Free PMC article.
DRPLA: An unusual disease or an underestimated cause of ataxia in Brazil?
Pinto WBVR, Salomão RPA, Bergamasco NC, da Cunha Ribas G, da Graça FF, Lopes-Cendes I, Bonadia L, de Souza PVS, Bulle Oliveira AS, Saraiva-Pereira ML, Jardim LB, Tumas V, Junior WM, França MC Jr, Pedroso JL, Barsottini OGP, Teive HAG. Pinto WBVR, et al. Among authors: bulle oliveira as. Parkinsonism Relat Disord. 2021 Nov;92:67-71. doi: 10.1016/j.parkreldis.2021.10.004. Epub 2021 Oct 11. Parkinsonism Relat Disord. 2021. PMID: 34700111
Intermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients.
Tavares de Andrade HM, Cintra VP, de Albuquerque M, Piccinin CC, Bonadia LC, Duarte Couteiro RE, Sabino de Oliveira D, Claudino R, Magno Gonçalves MV, Dourado MET Jr, de Souza LC, Teixeira AL, de Godoy Rousseff Prado L, Tumas V, Bulle Oliveira AS, Nucci A, Lopes-Cendes I, Marques W Jr, França MC Jr. Tavares de Andrade HM, et al. Among authors: bulle oliveira as. Neurobiol Aging. 2018 Sep;69:292.e15-292.e18. doi: 10.1016/j.neurobiolaging.2018.04.020. Epub 2018 May 8. Neurobiol Aging. 2018. PMID: 29934271
Teaching NeuroImages: Macrocerebellum and optic atrophy in a young boy.
de Rezende Pinto WB, de Souza PV, de Rezende Batistella GN, Bulle Oliveira AS. de Rezende Pinto WB, et al. Among authors: bulle oliveira as. Neurology. 2016 May 3;86(18):e201. doi: 10.1212/WNL.0000000000002643. Neurology. 2016. PMID: 27164656 No abstract available.
The expanding clinical and genetic spectrum of alsin-related disorders: the first cohort of Brazilian patients.
Alves De Siqueira Carvalho A, Antônio Troccoli Chieia M, Braga Farias I, Bulle Oliveira AS, Pinto WBVR, Souza PVS. Alves De Siqueira Carvalho A, et al. Among authors: bulle oliveira as. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Feb;23(1-2):16-24. doi: 10.1080/21678421.2021.1910306. Epub 2021 Nov 5. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 34738851 Review.
16 results