| dc.contributor.author | Bourbon, Mafalda | |
| dc.date.accessioned | 2019-02-18T17:36:46Z | |
| dc.date.available | 2019-02-18T17:36:46Z | |
| dc.date.issued | 2018-06 | |
| dc.description.abstract | Main Aim: To identify the cause of the dyslipidaemia in patients with a clinical phenotype of Familial Hypercholesterolaemia (FH). Secondary aims: To implement the genetic diagnosis of FH; To perform an epidemiological study of FH; To study the pathophysiology of premature CHD in FH patients. | pt_PT |
| dc.description.version | N/A | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.18/5877 | |
| dc.language.iso | eng | pt_PT |
| dc.publisher | Instituto Nacional de Saúde Doutor Ricardo Jorge, IP | pt_PT |
| dc.subject | Hipercolesterolemia Familiar | pt_PT |
| dc.subject | Dyslipidemia | pt_PT |
| dc.subject | FH in Portugal | pt_PT |
| dc.subject | Doenças Cardio e Cérebro-vasculares | pt_PT |
| dc.title | Estudo português de Hipercolesterolaemia Familiar | pt_PT |
| dc.type | lecture | |
| dspace.entity.type | Publication | |
| oaire.citation.conferencePlace | Lisboa, Portugal | pt_PT |
| oaire.citation.title | Aula no âmbito do Biosys PhD program, Science University, Lisbon, 26 June 2018 | pt_PT |
| rcaap.rights | closedAccess | pt_PT |
| rcaap.type | lecture | pt_PT |
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