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Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/353602
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dc.contributor.CRUESPUNIVERSIDADE ESTADUAL DE CAMPINASpt_BR
dc.contributor.authorunicampSecolin, Rodrigopt_BR
dc.contributor.authorunicampYasuda, Clarissa Linpt_BR
dc.contributor.authorunicampCendes, Fernandopt_BR
dc.contributor.authorunicampLopes-Cendes, Íscia Teresinhapt_BR
dc.typeArtigopt_BR
dc.titleGenetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patientspt_BR
dc.contributor.authorMcCormack, M.pt_BR
dc.contributor.authorGui, H.S.pt_BR
dc.contributor.authorIngason, A.pt_BR
dc.contributor.authorSpeed, D.pt_BR
dc.contributor.authorWright, G.E.B.pt_BR
dc.contributor.authorZhang, E.J.pt_BR
dc.contributor.authorSecolin, R.pt_BR
dc.contributor.authorYasuda, C.pt_BR
dc.contributor.authorKwok, M.pt_BR
dc.contributor.authorWolking, S.pt_BR
dc.contributor.authorBecker, F.pt_BR
dc.contributor.authorRau, S.pt_BR
dc.contributor.authorAvbersek, A.pt_BR
dc.contributor.authorHeggeli, K.pt_BR
dc.contributor.authorLeu, C.pt_BR
dc.contributor.authorDepondt, C.pt_BR
dc.contributor.authorSills, G.J.pt_BR
dc.contributor.authorMarson, A.G.pt_BR
dc.contributor.authorAuce, P.pt_BR
dc.contributor.authorBrpt_BR
dc.subjectAnticonvulsivantespt_BR
dc.subjectCarbamazepinapt_BR
dc.subjectEstudos de casos e controlespt_BR
dc.subjectFator H do complementopt_BR
dc.subjectErupção por drogapt_BR
dc.subjectAnticonvulsantspt_BR
dc.subjectCarbamazepinept_BR
dc.subjectCase-control studiespt_BR
dc.subjectComplement factor Hpt_BR
dc.subjectDrug eruptionspt_BR
dc.description.abstractTo characterize, among European and Han Chinese populations, the genetic predictors of maculopapular exanthema (MPE), a cutaneous adverse drug reaction common to antiepileptic drugs.We conducted a case-control genome-wide association study of autosomal gept_BR
dc.relation.ispartofNeurologypt_BR
dc.relation.ispartofabbreviationNeurologypt_BR
dc.publisher.cityPhiladelphia, PApt_BR
dc.publisher.countryEstados Unidospt_BR
dc.publisherOvid Technologies Wolters Kluwer Healthpt_BR
dc.date.issued2018pt_BR
dc.date.monthofcirculationJan.pt_BR
dc.language.isoengpt_BR
dc.description.volume90pt_BR
dc.description.issuenumber4pt_BR
dc.description.firstpagee332pt_BR
dc.description.lastpagee341pt_BR
dc.rightsFechadopt_BR
dc.sourceWOSpt_BR
dc.identifier.issn0028-3878pt_BR
dc.identifier.eissn1526-632Xpt_BR
dc.identifier.doi10.1212/WNL.0000000000004853pt_BR
dc.identifier.urlhttps://n.neurology.org/content/90/4/e332pt_BR
dc.description.sponsorshipFAPESP - FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULOpt_BR
dc.description.sponsorship1FAPESP - FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULOpt_BR
dc.description.sponsordocumentnumber2013/07559-3pt_BR
dc.date.available2021-01-04T20:49:21Z-
dc.date.accessioned2021-01-04T20:49:21Z-
dc.description.provenanceMade available in DSpace on 2021-01-04T20:49:21Z (GMT). No. of bitstreams: 1 000427799500009.pdf: 1225065 bytes, checksum: 44afcc4a57082e12e0dfc2742b58553c (MD5) Previous issue date: 2018en
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/353602-
dc.contributor.departmentsem informaçãopt_BR
dc.contributor.departmentDepartamento de Neurologiapt_BR
dc.contributor.departmentDepartamento de Neurologiapt_BR
dc.contributor.departmentDepartamento de Genética Médicapt_BR
dc.contributor.unidadeFaculdade de Ciências Médicaspt_BR
dc.contributor.unidadeFaculdade de Ciências Médicaspt_BR
dc.contributor.unidadeFaculdade de Ciências Médicaspt_BR
dc.contributor.unidadeFaculdade de Ciências Médicaspt_BR
dc.identifier.source000427799500009pt_BR
dc.creator.orcid0000-0002-2485-9560pt_BR
dc.creator.orcid0000-0001-9084-7173pt_BR
dc.creator.orcid0000-0001-9336-9568pt_BR
dc.creator.orcid0000-0002-6221-6822pt_BR
dc.type.formArtigo originalpt_BR
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