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Effect of statins on LDL particle size in patients with familial combined hyperlipidemia: a comparison between atorvastatin and pravastatin. 1-gen-2005 Sirtori, C. R.; Calabresi, L; Pisciotta, Livia; Cattin, L; Pauciullo, P; Montagnani, M; Manzato, E; BITTOLO BON, G; Fellin, R.
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families. 1-gen-2005 Calabresi, L; Pisciotta, Livia; Costantin, A; Frigerio, I; Eberini, I; Alessandrini, P; Arca, M; Bon, Gb; Boscutti, G; Busnach, G; Frascà, G; Gesualdo, L; Gigante, M; Lupattelli, G; Montali, A; Pizzolitto, S; Rabbone, I; Rolleri, M; Ruotolo, G; Sampietro, T; Sessa, A; Vaudo, G; Cantafora, A; Veglia, F; Calandra, S; Bertolini, Stefano; Franceschini, G.
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes 1-gen-2005 Pisciotta, Livia; Calabresi, L.; Lupattelli, G.; Siepi, G.; Mannarino, M. R.; Moleri, E.; Bellocchio, A.; Cantafora, A.; Tarugi, P.; Calandra, S.; Bertolini, Stefano
Serum homocysteine, methylenetetrahydrofolate reductase gene polymorphism and cardiovascular disease in heterozygous familial hypercholesterolemia. 1-gen-2005 Pisciotta, Livia; Cortese, C; Gnasso, A; Liberatoscioli, L; Pastore, A; Mannucci, L; Irace, C; Federici, G; Bertolini, Stefano
Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia. 1-gen-2005 Priore Oliva, C; Pisciotta, Livia; Li Volti, G; Sambataro, Mp; Cantafora, A; Bellocchio, A; Catapano, A; Tarugi, P; Bertolini, Stefano; Calandra, S.
Denaturing high-performance liquid chromatography (DHPLC) in the detection of mutations of ABCA1 gene in Familial HDL Deficiency. 1-gen-2005 Fasano, T; Bocchi, L; Pisciotta, Livia; Bertolini, Stefano; Calandra, S.
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia 1-gen-2006 Pisciotta, Livia; Oliva, Cp; Cefalu, Ab; Noto, D; Bellocchio, A; Fresa, R; Cantafora, A; Patel, D; Averna, M; Tarugi, P; Calandra, S; Bertolini, Stefano
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia. 1-gen-2006 Priore Oliva, C; Tarugi, P; Calandra, S; Pisciotta, Livia; Bellocchio, A; Bertolini, Stefano; Guardamagna, O; Schaap, Fg
Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): a phenotypic comparison. 1-gen-2006 Pisciotta, Livia; Oliva, Cp; Pes, Gm; DI SCALA, L; Bellocchio, A; Fresa, R; Cantafora, A; Arca, M; Calandra, S; Bertolini, Stefano
LCAT deficiency: molecular and phenotypic characterization of an Italian family. 1-gen-2006 Gigante, M; Ranieri, E; Cerullo, G; Calabresi, L; Iolascon, A; Assmann, G; Morrone, L; Pisciotta, Livia; Schena, Fp; Gesualdo, L.
Beta-sitosterolaemia: a new nonsense mutation in the ABCG5 gene. 1-gen-2007 Mannucci, L; Guardamagna, O; Bertucci, P; Pisciotta, Livia; Liberatoscioli, L; Bertolini, Stefano; Irace, C; Gnasso, A; Federici, G; Cortese, C.
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients. 1-gen-2007 Pisciotta, Livia; Fasano, T; Bellocchio, A; Bocchi, L; Sallo, R; Fresa, Raffaele; Colangeli, I; Cantafora, A; Calandra, S; Bertolini, Stefano
Molecular characterization of two patients with severe LCAT deficiency. 1-gen-2007 Charlton Menys, V; Pisciotta, Livia; Durrington, Pn; Neary, R; Short, Cd; Calabresi, L; Calandra, S; Bertolini, Stefano
Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs) 1-gen-2008 Aranda, P.; Valdivielso, P.; Pisciotta, Livia; Garcia, I.; Garcã, A. ARIAS C.; Bertolini, Stefano; Martã, N. REYES G.; GONZÃLEZ SANTOS, P.; Calandra, S.
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemia 1-gen-2008 Pisciotta, Livia; Fasano, T.; Calabresi, L.; Bellocchio, A.; Fresa, R.; Borrini, C.; Calandra, S.; Bertolini, Stefano
Severe HDL deficiency due to novel defects in the ABCA1 transporter. 1-gen-2009 Pisciotta, Livia; Bocchi, L.; Candini, C.; Sallo, R.; Zanotti, I.; Fasano, T.; Chakrapani, A.; Bates, T.; Bonardi, R.; Cantafora, A.; Ball, S.; Watts, G.; Bernini, F.; Calandra, S.; Bertolini, Stefano
An apparent inconsistency in parent to offspring transmission of point mutations of LDLR gene in familial hypercholesterolemia. 1-gen-2009 Rabacchi, C; Wunsch, A; Ghisellini, M; Marino, M; Pisciotta, Livia; Bertolini, Stefano; Calandra, S.
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene. 1-gen-2009 Pisciotta, Livia; Fresa, Raffaele; Bellocchio, A; Pino, E; Guido, V; Cantafora, A; Di Rocco, M; Calandra, S; Bertolini, Stefano
Traditional and non traditional risk factors in accelerated atherosclerosis in systemic lupus erythematosus: role of vascular endothelial growth factor (VEGATS Study). 1-gen-2009 Colombo, BARBARA MARIA; F., Cacciapaglia; M., Puntoni; Murdaca, Giuseppe; E., Rossi; Rodriguez, Guido; Nobili, FLAVIO MARIANO; Pisciotta, Livia; Bertolini, Stefano; T., Moccetti; F., Dentali; L., Steidl; G., Ciprandi; A., Afeltra; Indiveri, Francesco; Puppo, Francesco
The type of LDLR gene mutation predicts cardiovascular risk in children with familial hypercholesterolemia 1-gen-2009 Guardamagna, O.; Restagno, G.; Rolfo, E.; Pederiva, C.; Martini, S.; Abello, F.; Baracco, V.; Pisciotta, Livia; Pino, E.; Calandra, S.; Bertolini, Stefano
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