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Pharmacogenomics of dyslipidaemia drugs in Portugal

dc.contributor.authorChora, J.R.
dc.contributor.authorBourbon, M.
dc.date.accessioned2021-04-30T15:11:34Z
dc.date.available2021-04-30T15:11:34Z
dc.date.issued2020-10
dc.description.abstractBackground/Aim: Statins are the standard treatment for dyslipidaemia disorders, but there is a wide (10-70%) variation in patient response to statin treatment and several documented serious adverse effects. Studies of variants in genes regulating drug absorption, metabolism, pharmacodynamics and excretion mechanisms, have been implicated as reasons for this variability. The aim of this study is to determine the prevalence of pharmacogenetic relevant genotypes in the Portuguese population and in a sample of high cardiovascular risk patients: familial hypercholesterolemia subjects.pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/7718
dc.language.isoengpt_PT
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpt_PT
dc.subjectPharmacogenomicspt_PT
dc.subjectDyslipidemiapt_PT
dc.subjectPortugalpt_PT
dc.subjecte_CORpt_PT
dc.subjectFamilial Hypercholesterolaemiapt_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.titlePharmacogenomics of dyslipidaemia drugs in Portugalpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlace(online)pt_PT
oaire.citation.title88th European Atherosclerosis Society Congress, 4-7 October 2020pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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