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Author Report for: Pisciotta L

No contact information in database for Pisciotta L

    Title: Plasma HDL pattern, cholesterol efflux and cholesterol loading capacity of serum in carriers of a novel missense variant (Gly176Trp) of endothelial lipase
    Pisciotta L, Ossoli A, Ronca A, Garuti A, Fresa R, Favari E, Calabresi L, Calandra S, Bertolini S
    Ref: J Clin Lipidol, :, 2022 : PubMed


    Title: Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variants
    Pisciotta L, Tozzi G, Travaglini L, Taurisano R, Lucchi T, Indolfi G, Papadia F, Di Rocco M, D'Antiga L and Calandra S <7 more author(s)>
    Ref: Atherosclerosis, 265:124, 2017 : 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: Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrations
    Muntoni S, Wiebusch H, Jansen-Rust M, Rust S, Schulte H, Berger K, Pisciotta L, Bertolini S, Funke H and Assmann G <1 more author(s)>
    Ref: Nutr Metab Cardiovasc Dis, 23:732, 2013 : PubMed


    Title: A three month-old infant with severe hyperchylomicronemia: Molecular diagnosis and extracorporeal treatment
    Stefanutti C, Gozzer M, Pisciotta L, D'Eufemia P, Bosco G, Morozzi C, Papadia F, Shafii M, Di Giacomo S, Bertolini S
    Ref: Atheroscler Suppl, 14:73, 2013 : PubMed


    Title: Lysosomal lipase deficiency: molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease
    Fasano T, Pisciotta L, Bocchi L, Guardamagna O, Assandro P, Rabacchi C, Zanoni P, Filocamo M, Bertolini S, Calandra S
    Ref: Mol Genet Metab, 105:450, 2012 : PubMed


    Title: Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene
    Pisciotta L, Fresa R, Bellocchio A, Pino E, Guido V, Cantafora A, Di Rocco M, Calandra S, Bertolini S
    Ref: Mol Genet Metab, 97:143, 2009 : PubMed


    Title: Molecular characterization of two patients with severe LCAT deficiency
    Charlton-Menys V, Pisciotta L, Durrington PN, Neary R, Short CD, Calabresi L, Calandra S, Bertolini S
    Ref: Nephrol Dial Transplant, 22:2379, 2007 : PubMed


    Title: The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families
    Calabresi L, Pisciotta L, Costantin A, Frigerio I, Eberini I, Alessandrini P, Arca M, Bon GB, Boscutti G and Franceschini G <17 more author(s)>
    Ref: Arterioscler Thromb Vasc Biol, 25:1972, 2005 : PubMed


    Title: A 33-year-old man with nephrotic syndrome and lecithin-cholesterol acyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT gene
    Frasca GM, Soverini L, Tampieri E, Franceschini G, Calabresi L, Pisciotta L, Preda P, Vangelista A, Stefoni S, Bertolini S
    Ref: Nephrol Dial Transplant, 19:1622, 2004 : 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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Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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