Nobrega PR - Search Results

1

Homozygous missense mutation in MED25 segregates with syndromic intellectual disability in a large consanguineous family.

Figueiredo T, Melo US, Pessoa AL, Nobrega PR, Kitajima JP, Correa I, Zatz M, Kok F, Santos S. Figueiredo T, et al. Among authors: nobrega pr. J Med Genet. 2015 Feb;52(2):123-7. doi: 10.1136/jmedgenet-2014-102793. Epub 2014 Dec 19. J Med Genet. 2015. PMID: 25527630

2

Brazilian consensus recommendations on the diagnosis and treatment of autoimmune encephalitis in the adult and pediatric populations.

Dutra LA, Silva PVC, Ferreira JHF, Marques AC, Toso FF, Vasconcelos CCF, Brum DG, Pereira SLDA, Adoni T, Rocha LJA, Sampaio LPB, Sousa NAC, Paolilo RB, Pizzol AD, Costa BKD, Disserol CCD, Pupe C, Valle DAD, Diniz DS, Abrantes FF, Schmidt FDR, Cendes F, Oliveira FTM, Martins GJ, Silva GD, Lin K, Pinto LF, Santos MLSF, Gonçalves MVM, Krueger MB, Haziot MEJ, Barsottini OGP, Nascimento OJMD, Nóbrega PR, Proveti PM, Castilhos RMD, Daccach V, Glehn FV. Dutra LA, et al. Among authors: nobrega pr. Arq Neuropsiquiatr. 2024 Jul;82(7):1-15. doi: 10.1055/s-0044-1788586. Epub 2024 Aug 1. Arq Neuropsiquiatr. 2024. PMID: 39089672 Free article. English.

3

Spinal cord compression by cystic IgG4-related spinal pachymeningitis mimicking neurocysticercosis: a case report.

Araújo DABS, Ribeiro RM, Lima PLGSB, de Queiroz DC, Pitombeira MS, Martins B, Coimbra PPA, Nogueira CD, Braga-Neto P, Silva GD, Nóbrega PR. Araújo DABS, et al. Among authors: nobrega pr. BMC Neurol. 2024 Sep 5;24(1):318. doi: 10.1186/s12883-024-03817-7. BMC Neurol. 2024. PMID: 39237872 Free PMC article.

4

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids (SLIPPERS)-Does it Really Exist?

Freua F, Mahler JV, Lima PLGSB, Neville IS, Portella LB, Marussi VHR, Lancellotti CLP, Nobrega PR, Silva GD. Freua F, et al. Among authors: nobrega pr. Brain Sci. 2023 Aug 11;13(8):1191. doi: 10.3390/brainsci13081191. Brain Sci. 2023. PMID: 37626547 Free PMC article.

5

Central hypersomnia and chronic insomnia: expanding the spectrum of sleep disorders in long COVID syndrome - a prospective cohort study.

Moura AEF, Oliveira DN, Torres DM, Tavares-Júnior JWL, Nóbrega PR, Braga-Neto P, Sobreira-Neto MA. Moura AEF, et al. Among authors: nobrega pr. BMC Neurol. 2022 Nov 9;22(1):417. doi: 10.1186/s12883-022-02940-7. BMC Neurol. 2022. PMID: 36352367 Free PMC article.

6

Correlation between ABO blood type, susceptibility to SARS-CoV-2 infection and COVID-19 disease severity: A systematic review.

Soares DMB, Araújo DABS, de Souza JLB, Maurício RB, Soares EMB, Neto FCA, Pinheiro MSN, Gama VCV, Braga-Neto P, Nóbrega PR, Aragão GF. Soares DMB, et al. Among authors: nobrega pr. Hematol Transfus Cell Ther. 2023 Oct-Dec;45(4):483-494. doi: 10.1016/j.htct.2022.11.001. Epub 2022 Nov 30. Hematol Transfus Cell Ther. 2023. PMID: 36467112 Free PMC article. Review.

7

A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability.

Figueiredo T, Melo US, Pessoa AL, Nobrega PR, Kitajima JP, Rusch H, Vaz F, Lucato LT, Zatz M, Kok F, Santos S. Figueiredo T, et al. Among authors: nobrega pr. Mol Psychiatry. 2016 Aug;21(8):1125-9. doi: 10.1038/mp.2015.150. Epub 2015 Sep 29. Mol Psychiatry. 2016. PMID: 26416544

8

A novel GFAP mutation in a type II (late-onset) Alexander disease patient.

de Paiva AR, Freua F, Lucato LT, Parmera J, Dória D, Nóbrega PR, Olávio TR, Macedo-Souza LI, Kok F. de Paiva AR, et al. Among authors: nobrega pr. J Neurol. 2016 Apr;263(4):821-2. doi: 10.1007/s00415-016-8065-8. Epub 2016 Feb 25. J Neurol. 2016. PMID: 26914930 No abstract available.

9

High phenotypic variability in Gerstmann-Sträussler-Scheinker disease.

Smid J, Studart A Neto, Landemberger MC, Machado CF, Nóbrega PR, Canedo NHS, Schultz RR, Naslavsky MS, Rosemberg S, Kok F, Chimelli L, Martins VR, Nitrini R. Smid J, et al. Among authors: nobrega pr. Arq Neuropsiquiatr. 2017 Jun;75(6):331-338. doi: 10.1590/0004-282X20170049. Arq Neuropsiquiatr. 2017. PMID: 28658400 Free article.

10

Loss-of-function mutation in inositol monophosphatase 1 (IMPA1) results in abnormal synchrony in resting-state EEG.

Walker CP, Pessoa ALS, Figueiredo T, Rafferty M, Melo US, Nóbrega PR, Murphy N, Kok F, Zatz M, Santos S, Cho RY. Walker CP, et al. Among authors: nobrega pr. Orphanet J Rare Dis. 2019 Jan 7;14(1):3. doi: 10.1186/s13023-018-0977-1. Orphanet J Rare Dis. 2019. PMID: 30616629 Free PMC article.

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