Tarugi P

References (6)

Title : Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride - Buonuomo_2017_J.Clin.Lipidol_11_1329
Author(s) : Buonuomo PS , Rabacchi C , Macchiaiolo M , Trenti C , Fasano T , Tarugi P , Bartuli A , Bertolini S , Calandra S
Ref : J Clin Lipidol , 11 :1329 , 2017
Abstract :
PubMedSearch : Buonuomo_2017_J.Clin.Lipidol_11_1329
PubMedID: 28951076
Gene_locus related to this paper: human-LIPC , human-LPL

Title : Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene - Rabacchi_2016_J.Clin.Lipidol_10_915
Author(s) : Rabacchi C , D'Addato S , Palmisano S , Lucchi T , Bertolini S , Calandra S , Tarugi P
Ref : J Clin Lipidol , 10 :915 , 2016
Abstract :
PubMedSearch : Rabacchi_2016_J.Clin.Lipidol_10_915
PubMedID: 27578123

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 : Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia - Conca_2012_J.Clin.Lipidol_6_244
Author(s) : Conca P , Pileggi S , Simonelli S , Boer E , Boscutti G , Magnolo L , Tarugi P , Penco S , Franceschini G , Calabresi L , Gomaraschi M
Ref : J Clin Lipidol , 6 :244 , 2012
Abstract :
PubMedSearch : Conca_2012_J.Clin.Lipidol_6_244
PubMedID: 22658148
Gene_locus related to this paper: human-LCAT

Title : Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia - Cefalu_2009_J.Clin.Endocrinol.Metab_94_4584
Author(s) : Cefalu AB , Noto D , Arpi ML , Yin F , Spina R , Hilden H , Barbagallo CM , Carroccio A , Tarugi P , Squatrito S , Vigneri R , Taskinen MR , Peterfy M , Averna MR
Ref : J Clinical Endocrinology Metab , 94 :4584 , 2009
Abstract :
PubMedSearch : Cefalu_2009_J.Clin.Endocrinol.Metab_94_4584
PubMedID: 19820022

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