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Author Report for: Tarugi P

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    Title: Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride
    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 : PubMed

            

    Title: Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene
    Rabacchi C, D'Addato S, Palmisano S, Lucchi T, Bertolini S, Calandra S, Tarugi P
    Ref: J Clin Lipidol, 10:915, 2016 : PubMed

            

    Title: Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia
    Rabacchi C, Pisciotta L, Cefalu AB, Noto D, Fresa R, Tarugi P, Averna M, Bertolini S, Calandra S
    Ref: Atherosclerosis, 241:79, 2015 : PubMed

            

    Title: Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia
    Conca P, Pileggi S, Simonelli S, Boer E, Boscutti G, Magnolo L, Tarugi P, Penco S, Franceschini G and Gomaraschi M <1 more author(s)>
    Ref: J Clin Lipidol, 6:244, 2012 : PubMed

            

    Title: Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia
    Cefalu AB, Noto D, Arpi ML, Yin F, Spina R, Hilden H, Barbagallo CM, Carroccio A, Tarugi P and Averna MR <4 more author(s)>
    Ref: J Clinical Endocrinology Metab, 94:4584, 2009 : PubMed

            

    Title: Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders
    Pisciotta L, Hamilton-Craig I, Tarugi P, Bellocchio A, Fasano T, Alessandrini P, Bon GB, Siepi D, Mannarino E and Bertolini S <5 more author(s)>
    Ref: Atherosclerosis, 172:309, 2004 : PubMed

            


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