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Brazilian Position Statement for Familial Chylomicronemia Syndrome - 2023.
Arq Bras Cardiol. 2023 Mar;120(4):e20230203. doi: 10.36660/abc.20230203.
Arq Bras Cardiol. 2023.
PMID: 37075362
Free PMC article.
English, Portuguese.
No abstract available.
A novel GPIHBP1 mutation related to familial chylomicronemia syndrome: A series of cases.
Lima JG, Helena C Nobrega L, Moura Bandeira FT, Pires Sousa AG, Medeiros de Araujo Macedo TB, Cavalcante Nogueira AC, Fernandes de Oliveira Filho A, Alves RJ, Costa Gurgel Castelo MH, Silva Coelho FM, Maia RE, Lima DN, Timoteo ARS, de Melo Campos JTA.
Lima JG, et al. Among authors: maia re.
Atherosclerosis. 2021 Apr;322:31-38. doi: 10.1016/j.atherosclerosis.2021.02.020. Epub 2021 Feb 23.
Atherosclerosis. 2021.
PMID: 33706081
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A brazilian nationwide multicenter study on deficiency of deaminase-2 (DADA2).
Melo A, de Carvalho LM, Ferriani VPL, Cavalcanti A, Appenzeller S, Oliveira VR, Neto HC, Rosário NA, de Oliveira Poswar F, Guimaraes MX, Kokron CM, Maia RE, Silva GD, Keller G, Ferreira MD, Vasconcelos DM, Toledo-Barros MAM, Barros SF, Neto NSR, Krieger MH, Kalil J, Mendonça LO.
Melo A, et al. Among authors: maia re.
Adv Rheumatol. 2023 May 22;63(1):23. doi: 10.1186/s42358-023-00303-5.
Adv Rheumatol. 2023.
PMID: 37217999
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Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).
Félix TM, de Oliveira BM, Artifon M, Carvalho I, Bernardi FA, Schwartz IVD, Saute JA, Ferraz VEF, Acosta AX, Sorte NB, Alves D; RARAS Network group.
Félix TM, et al.
Orphanet J Rare Dis. 2022 Feb 24;17(1):84. doi: 10.1186/s13023-022-02254-4.
Orphanet J Rare Dis. 2022.
PMID: 35209917
Free PMC article.
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Ionic Channels as Potential Targets for the Treatment of Autism Spectrum Disorder: A Review.
da Silva PR, do Nascimento Gonzaga TKS, Maia RE, da Silva BA.
da Silva PR, et al. Among authors: maia re.
Curr Neuropharmacol. 2022;20(10):1834-1849. doi: 10.2174/1570159X19666210809102547.
Curr Neuropharmacol. 2022.
PMID: 34370640
Free PMC article.
Review.
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