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Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease. 1-gen-2010 Bocchi, L; Pisciotta, Livia; Fasano, T; Candini, C; Puntoni, Mr; Sampietro, T; Bertolini, Stefano; Calandra, S.
Pseudoxanthoma elasticum and familial hypercholesterolemia: A deleterious combination of cardiovascular risk factors 1-gen-2010 Pisciotta, Livia; Tarugi, P.; Borrini, C.; Bellocchio, A.; Fresa, R.; Guerra, D.; Quaglino, D.; Ronchetti, I.; Calandra, S.; Bertolini, Stefano
Two novel rare variants of APOA5 gene found in subjects with severe hypertrigliceridemia. 1-gen-2011 Pisciotta, Livia; R., Fresa; A., Bellocchio; V., Guido; C., Priore Oliva; S., Calandra; Bertolini, Stefano
Characterization of Three Kindred with Familial Combined Hypolipidemia Due to Loss of Function Mutations of ANGPTL3. 1-gen-2011 Pisciotta, Livia; Favari, E; Magnolo, Al; Simonelli, S; Adorni, Mp; Sallo, R; Fancello, T; Zavaroni, I; Ardigò, D; Bernini, F; Calabresi, L; Franceschini, G; Tarugi, P; Calandra, S; Bertolini, Stefano
Hypoalpha-hypobetalipoproteinemia (Familial Combined Hypolipidemia) caused by loss of function mutations of ANGPTL3 gene. 1-gen-2011 Pisciotta, L; Di Leo, E; Tarugi, P; Fresa, R; Zavaroni, I; Ardigò, D; Guido, V; Bertolini, S; Calandra, S
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease. 1-gen-2011 Fasano, T; Pisciotta, Livia; Bocchi, L; Guardamagna, O; Assandro, P; Rabacchi, C; Zanoni, P; Filocamo, M; Bertolini, Stefano; Calandra, S.
Nutraceutical pill containing berberine versus ezetimibe on plasma lipid pattern in hypercholesterolemic subjects and its additive effect in patients with familial hypercholesterolemia on stable cholesterol-lowering treatment. 1-gen-2012 Pisciotta, Livia; Bellocchio, A; Bertolini, Stefano
Leucine 10 allelic variant in signal peptide of PCSK9 increases the LDL cholesterol-lowering effect of statins in patients with familial hypercholesterolaemia. 1-gen-2012 Pisciotta, Livia; Sallo, R; Rabacchi, C; Wunsch, A; Calandra, S; Bertolini, Stefano
Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency. 1-gen-2012 Fasano, T; Zanoni, P; Rabacchi, C; Pisciotta, Livia; Favari, E; Adorni, Mp; Deegan, Pb; Park, A; Hlaing, T; Feher, Md; Jones, B; Uzak, As; Kardas, F; Dardis, A; Sechi, A; Bembi, B; Minuz, P; Bertolini, Stefano; Bernini, F; Calandra, S.
A silent mutation of Niemann-Pick C1-like 1 and apolipoprotein E4 modulate cholesterol absorption in primary hyperlipidemias. 1-gen-2013 Lupattelli, G; Pisciotta, Livia; De Vuono, S; Siepi, D; Bellocchio, A; Melis, F; Bertolini, Stefano; Pirro, M; Mannarino, E.
Lipoprotein glomerulopathy associated with a mutation in apolipoprotein e. 1-gen-2013 Magistroni, R; Bertolotti, M; Furci, L; Fano, Ra; Leonelli, M; Pisciotta, Livia; Pellegrini, E; Calabresi, L; Bertolini, Stefano; Calandra, S.
A three month-old infant with severe hyperchylomicronemia: molecular diagnosis and extracorporeal treatment. 1-gen-2013 Stefanutti, C; Gozzer, M; Pisciotta, Livia; D'Eufemia, P; Bosco, G; Morozzi, C; Papadia, F; Shafii, M; Di Giacomo, S; Bertolini, Stefano
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy. 1-gen-2013 Bertolini, S; Pisciotta, L; Rabacchi, C; Cefalù, Ab; Noto, D; Fasano, T; Signori, A; Fresa, R; Averna, M; Calandra, S
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis. 1-gen-2013 Minicocci, I; Santini, S; Cantisani, V; Stitziel, N; Kathiresan, S; Arroyo, Ja; Martí, G; Pisciotta, Livia; Noto, D; Cefalù, Ab; Maranghi, M; Labbadia, G; Pigna, G; Pannozzo, F; Ceci, F; Ciociola, E; Bertolini, Stefano; Calandra, S; Tarugi, P; Averna, M; Arca, M.
Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrations. 1-gen-2013 Muntoni, S; Wiebusch, H; Jansen Rust, M; Rust, S; Schulte, H; Berger, K; Pisciotta, Livia; Bertolini, Stefano; Funke, H; Seedorf, U; Assmann, G.
Lipoprotein Glomerulopathy: molecular chatacterization of three Italian patients and literature survey. 1-gen-2014 Pasquariello A, 1. 4. 6.; Pisciotta, Livia; Sampietro, T; Pasquariello, G; Masiello, P; Masini, M; Sbrana, F; Puntoni, M; Miccoli, R; Calandra, S; Bertolini, Stefano
Pharmacological treatment of a Sardinian patient affected by autosomal recessive hypercholesterolemia (ARH) 1-gen-2015 Sandro, Muntoni; Pisciotta, Livia; Sergio, Muntoni; Bertolini, Stefano
Testing the Short-Term Efficacy of a Lipid-Lowering Nutraceutical in the Setting of Clinical Practice: A Multicenter Study 1-gen-2015 Cicero, Arrigo F. G; Derosa, Giuseppe; Pisciotta, Livia; Barbagallo, Carlo
Carotid ultrasonography in the assessment of cardiovascular risk 1-gen-2015 Pende, Aldo; Artom, Nathan; Pistocchi, Giovanni; Pisciotta, Livia; Dallegri, Franco
Lipoproteins, stroke and statins. 1-gen-2015 Pisciotta, Livia; Bertolini, Stefano; Pende, Aldo
Mostrati risultati da 41 a 60 di 128
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