Publication
Lysossomal acid lipase activity in dried blood spots - preliminar results
| dc.contributor.author | Gaspar, Paulo | |
| dc.contributor.author | Alves, Sandra | |
| dc.contributor.author | Vilarinho, Laura | |
| dc.date.accessioned | 2018-04-04T14:51:01Z | |
| dc.date.available | 2018-04-04T14:51:01Z | |
| dc.date.issued | 2017-03 | |
| dc.description.abstract | Lysosomal storage diseases (LSDs) are a group of heterogeneous and multisystemic disorders caused by defects in enzymes responsible for the intralysosomal degradation of particular compounds. One of them is Lysosomal Acid Lipase Deficiency (LALD) that is caused by the deficiency of the enzyme Lysosomal Acid Lipase (LAL), which is responsible for the hydrolysis of cholesterol esters and triglycerides in the lysosome. | pt_PT |
| dc.description.version | N/A | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.18/5526 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.subject | Doenças Lisossomais de Sobrecarga | pt_PT |
| dc.subject | Lipase Ácida | pt_PT |
| dc.subject | Doenças Genéticas | pt_PT |
| dc.subject | Doença de Wolman | pt_PT |
| dc.title | Lysossomal acid lipase activity in dried blood spots - preliminar results | pt_PT |
| dc.type | conference object | |
| dspace.entity.type | Publication | |
| oaire.citation.conferencePlace | Évora, Portugal | pt_PT |
| oaire.citation.title | 13th International Symposium of SPDM (Sociedade Portuguesa de Doenças Metabólicas), 16-17 March 2017 | pt_PT |
| rcaap.rights | openAccess | pt_PT |
| rcaap.type | conferenceObject | pt_PT |