Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.18/5566
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dc.contributor.authorAbrantes, LB.-
dc.contributor.authorAlves, A.C.-
dc.contributor.authorMedeiros, A.M.-
dc.contributor.authorCorreia, S.-
dc.contributor.authorCruz, A.-
dc.contributor.authorLobarinhas, G.-
dc.contributor.authorGarcia, P.-
dc.contributor.authorGuerra, A.-
dc.contributor.authorMansilha, H.-
dc.contributor.authorMartins, E.-
dc.contributor.authorMartins, P.-
dc.contributor.authorSalgado, J.-
dc.contributor.authorBourbon, M.-
dc.contributor.authoron behalf of investigators of Portuguese FH study-
dc.date.accessioned2018-06-07T13:53:48Z-
dc.date.available2018-06-07T13:53:48Z-
dc.date.issued2018-05-
dc.identifier.urihttp://hdl.handle.net/10400.18/5566-
dc.description.abstractThe Portuguese FH Study (PFHS) started in 1999. The aim of the PFHS is to identify the cause of dyslipidemia in patients with a clinical diagnosis of FH. To date, 452 pediatric patients were referred to us, 288 of which are index patients. The aim of this study was to analyse the lipid profile and molecular diagnosis of children recruited for the PFHS.pt_PT
dc.description.sponsorshipAbrantes LB. acknowledges grant BioMolecular/09/2017pt_PT
dc.language.isoengpt_PT
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpt_PT
dc.rightsembargoedAccesspt_PT
dc.subjectPortuguese FH Studypt_PT
dc.subjectDyslipidemiapt_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.titleCharacterization of pediatric patients from Portuguese FH studypt_PT
dc.typeconferenceObjectpt_PT
dc.description.versionN/Apt_PT
degois.publication.locationLisbon, Portugalpt_PT
degois.publication.title2nd EAS Pediatric Familial Hypercholesterolemia Symposium, May 9 2018pt_PT
Aparece nas colecções:DPSPDNT - Posters/abstracts em congressos internacionais

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