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Polymorphisms in the CIITA -168A/G (rs3087456) and CIITA +1614G/C (rs4774) may influence severity in multiple sclerosis patients.
Pereira VCSR, Fontes-Dantas FL, Paradela ER, Malfetano FR, Scherpenhuijzen SSB, Mansur LF, Luiz RR, Oliveira AP, Farinhas JGD, Maiolino Â, Alves-Leon SV. Pereira VCSR, et al. Among authors: paradela er. Arq Neuropsiquiatr. 2019 Mar;77(3):166-173. doi: 10.1590/0004-282X20190026. Arq Neuropsiquiatr. 2019. PMID: 30970129 Free article.
Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
Agostinho Lde A, Rocha CF, Medina-Acosta E, Barboza HN, da Silva AF, Pereira SP, da Silva Idos S, Paradela ER, Figueiredo AL, Nogueira Ede M, Alvarenga RM, Hernan Cabello P, dos Santos SR, Paiva CL. Agostinho Lde A, et al. Among authors: paradela er. J Hum Genet. 2012 Dec;57(12):796-803. doi: 10.1038/jhg.2012.120. Epub 2012 Oct 11. J Hum Genet. 2012. PMID: 23051704
The CIITA genetic polymorphism rs4774*C in combination with the HLA-DRB1*15:01 allele as a putative susceptibility factor to multiple sclerosis in Brazilian females.
Paradela ER, Alves-Leon SV, Figueiredo AL, Pereira VC, Malfetano F, Mansur LF, Scherpenhuijzen S, Agostinho LA, Rocha CF, Rueda-Lopes F, Gasparetto E, Paiva CL. Paradela ER, et al. Arq Neuropsiquiatr. 2015 Apr;73(4):283-8. doi: 10.1590/0004-282X20150012. Epub 2015 Apr 1. Arq Neuropsiquiatr. 2015. PMID: 25992516 Free article.