BOCCHI, Letizia
BOCCHI, Letizia
Dip. SCIENZE BIO-MEDICHE (attivo dal 01/01/1900 al 29/06/2012)
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol
2007-01-01 Fasano, Tommaso; Cefalu, Ab; Di Leo, E; Noto, D; Pollaccia, D; Bocchi, Letizia; Valenti, V; Bonardi, R; Guardamagna, O; Averna, M; Tarugi, Patrizia Maria
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency
2005-01-01 Fasano, Tommaso; Bocchi, Letizia; L., Pisciotta; S., Bertolini; CALANDRA BUONAURA, Sebastiano
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients
2007-01-01 Pisciotta, L; Fasano, Tommaso; Bellocchio, A; Bocchi, Letizia; Sallo, R; Fresa, R; Colangeli, I; Cantafora, A; CALANDRA BUONAURA, Sebastiano; Bertolini, S.
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans
2009-01-01 Calabresi, L; Baldassarre, D; Castelnuovo, S; Conca, P; Bocchi, Letizia; Candini, Chiara; Frigerio, B; Amato, M; Sirtori, Cr; Alessandrini, P; Arca, M; Boscutti, G; Cattin, L; Gesualdo, L; Sampietro, T; Vaudo, G; Veglia, F; CALANDRA BUONAURA, Sebastiano; Franceschini, G.
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol.
2010-01-01 Candini, Chiara; Schimmel, Aw; Peter, J; Bochem, Ae; Holleboom, Ag; Vergeer, M; Dullaart, Rp; Dallinga Thie, Gm; Hovingh, Gk; Khoo, Kl; Fasano, Tommaso; Bocchi, Letizia; CALANDRA BUONAURA, Sebastiano; Kuivenhoven, Ja; Motazacker, M. M.
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease
2012-01-01 Fasano, Tommaso; Pisciotta, L; Bocchi, Letizia; Guardamagna, O; Assandro, P; Rabacchi, Claudio; Zanoni, Paolo; Filocamo, M; Bertolini, S; CALANDRA BUONAURA, Sebastiano
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease.
2010-01-01 Bocchi, Letizia; Pisciotta, L; Fasano, Tommaso; Candini, Chiara; Puntoni, Mr; Sampietro, T; Bertolini, S; CALANDRA BUONAURA, Sebastiano
Severe HDL deficiency due to novel defects in the ABCA1 transporter
2009-01-01 Pisciotta, L; Bocchi, Letizia; Candini, Chiara; Sallo, R; Zanotti, I; Fasano, Tommaso; Chakrapani, A; Bates, T; Bonardi, R; Cantafora, A; Ball, S; Watts, G; Bernini, F; CALANDRA BUONAURA, Sebastiano; Bertolini, S.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol | 1-gen-2007 | Fasano, Tommaso; Cefalu, Ab; Di Leo, E; Noto, D; Pollaccia, D; Bocchi, Letizia; Valenti, V; Bonardi, R; Guardamagna, O; Averna, M; Tarugi, Patrizia Maria | |
| Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency | 1-gen-2005 | Fasano, Tommaso; Bocchi, Letizia; L., Pisciotta; S., Bertolini; CALANDRA BUONAURA, Sebastiano | |
| Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients | 1-gen-2007 | Pisciotta, L; Fasano, Tommaso; Bellocchio, A; Bocchi, Letizia; Sallo, R; Fresa, R; Colangeli, I; Cantafora, A; CALANDRA BUONAURA, Sebastiano; Bertolini, S. | |
| Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans | 1-gen-2009 | Calabresi, L; Baldassarre, D; Castelnuovo, S; Conca, P; Bocchi, Letizia; Candini, Chiara; Frigerio, B; Amato, M; Sirtori, Cr; Alessandrini, P; Arca, M; Boscutti, G; Cattin, L; Gesualdo, L; Sampietro, T; Vaudo, G; Veglia, F; CALANDRA BUONAURA, Sebastiano; Franceschini, G. | |
| Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol. | 1-gen-2010 | Candini, Chiara; Schimmel, Aw; Peter, J; Bochem, Ae; Holleboom, Ag; Vergeer, M; Dullaart, Rp; Dallinga Thie, Gm; Hovingh, Gk; Khoo, Kl; Fasano, Tommaso; Bocchi, Letizia; CALANDRA BUONAURA, Sebastiano; Kuivenhoven, Ja; Motazacker, M. M. | |
| Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease | 1-gen-2012 | Fasano, Tommaso; Pisciotta, L; Bocchi, Letizia; Guardamagna, O; Assandro, P; Rabacchi, Claudio; Zanoni, Paolo; Filocamo, M; Bertolini, S; CALANDRA BUONAURA, Sebastiano | |
| 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, Letizia; Pisciotta, L; Fasano, Tommaso; Candini, Chiara; Puntoni, Mr; Sampietro, T; Bertolini, S; CALANDRA BUONAURA, Sebastiano | |
| Severe HDL deficiency due to novel defects in the ABCA1 transporter | 1-gen-2009 | Pisciotta, L; Bocchi, Letizia; Candini, Chiara; Sallo, R; Zanotti, I; Fasano, Tommaso; Chakrapani, A; Bates, T; Bonardi, R; Cantafora, A; Ball, S; Watts, G; Bernini, F; CALANDRA BUONAURA, Sebastiano; Bertolini, S. |