| Title : Diagnostic algorithm for familial chylomicronemia syndrome - Stroes_2017_Atheroscler.Suppl_23_1 |
| Author(s) : Stroes E , Moulin P , Parhofer KG , Rebours V , Lohr JM , Averna M |
| Ref : Atheroscler Suppl , 23 :1 , 2017 |
| Abstract : |
| PubMedSearch : Stroes_2017_Atheroscler.Suppl_23_1 |
| PubMedID: 27998715 |
| Title : Severe reduction of blood lysosomal acid lipase activity in cryptogenic cirrhosis: A nationwide multicentre cohort study - Angelico_2017_Atherosclerosis_262_179 |
| Author(s) : Angelico F , Corradini SG , Pastori D , Fargion S , Fracanzani AL , Angelico M , Bolondi L , Tozzi G , Pujatti PL , Labbadia G , Corazza GR , Averna M , Perticone F , Croce G , Persico M , Bucci T , Baratta F , Polimeni L , Del Ben M , Violi F |
| Ref : Atherosclerosis , 262 :179 , 2017 |
| Abstract : |
| PubMedSearch : Angelico_2017_Atherosclerosis_262_179 |
| PubMedID: 28396038 |
| Title : Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia - Rabacchi_2015_Atherosclerosis_241_79 |
| Author(s) : Rabacchi C , Pisciotta L , Cefalu AB , Noto D , Fresa R , Tarugi P , Averna M , Bertolini S , Calandra S |
| Ref : Atherosclerosis , 241 :79 , 2015 |
| Abstract : |
| PubMedSearch : Rabacchi_2015_Atherosclerosis_241_79 |
| PubMedID: 25966443 |
| Gene_locus related to this paper: human-LPL |
| Title : Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders - Pisciotta_2004_Atherosclerosis_172_309 |
| Author(s) : Pisciotta L , Hamilton-Craig I , Tarugi P , Bellocchio A , Fasano T , Alessandrini P , Bon GB , Siepi D , Mannarino E , Cattin L , Averna M , Cefalu AB , Cantafora A , Calandra S , Bertolini S |
| Ref : Atherosclerosis , 172 :309 , 2004 |
| Abstract : |
| PubMedSearch : Pisciotta_2004_Atherosclerosis_172_309 |
| PubMedID: 15019541 |