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matia re
(9 results)?
A brazilian nationwide multicenter study on deficiency of deaminase-2 (DADA2).
Adv Rheumatol. 2023 May 22;63(1):23. doi: 10.1186/s42358-023-00303-5.
Adv Rheumatol. 2023.
PMID: 37217999
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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Brazilian Position Statement for Familial Chylomicronemia Syndrome - 2023.
Izar MCO, Santos Filho RDD, Assad MHV, Chagas ACP, Toledo Júnior AO, Nogueira ACC, Souto ACCF, Lottenberg AMP, Chacra APM, Ferreira CEDS, Lourenço CM, Valerio CM, Cintra DE, Fonseca FAH, Campana GA, Bianco HT, Lima JG, Castelo MHCG, Scartezini M, Moretti MA, Barreto NSF, Maia RE, Montenegro Junior RM, Alves RJ, Figueiredo RMM, Fock RA, Martinez TLDR.
Izar MCO, et al. Among authors: maia re.
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.
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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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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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