Publication
How to avoid the differential diagnostic odyssey
| dc.contributor.author | Bourbon, Mafalda | |
| dc.date.accessioned | 2019-03-08T15:27:41Z | |
| dc.date.available | 2019-03-08T15:27:41Z | |
| dc.date.issued | 2018-05 | |
| dc.description | Comunicação a convite. | pt_PT |
| dc.description.abstract | Familial Hypercholesterolemia is the most common monogenic dyslipidemia: Heterozygote prevalence: 1/250 − 1/500; Homozygous is more rare: 1/300000 − 1/1,000000 | pt_PT |
| dc.description.sponsorship | Mafalda Bourbon has received project grants from Praxis, Synageva/Alexion, Regeneron and Gendiag | pt_PT |
| dc.description.version | N/A | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.18/6103 | |
| dc.language.iso | eng | pt_PT |
| dc.publisher | Instituto Nacional de Saúde Doutor Ricardo Jorge, IP | pt_PT |
| dc.subject | Familial Hypercholesterolemia | pt_PT |
| dc.subject | Portuguese FH Study | pt_PT |
| dc.subject | Doenças Cardio e Cérebro-vasculares | pt_PT |
| dc.title | How to avoid the differential diagnostic odyssey | pt_PT |
| dc.type | conference object | |
| dspace.entity.type | Publication | |
| oaire.citation.conferencePlace | Lisboa, Portugal | pt_PT |
| oaire.citation.title | 86th European Atherosclerosis Society Congress, 5-08 May 2018 | pt_PT |
| rcaap.rights | embargoedAccess | pt_PT |
| rcaap.type | conferenceObject | pt_PT |
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