Calabresi L - Search Results

1

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. Pisciotta L, et al. Among authors: calabresi l. J Clin Lipidol. 2022 Sep-Oct;16(5):694-703. doi: 10.1016/j.jacl.2022.08.002. Epub 2022 Aug 12. J Clin Lipidol. 2022. PMID: 36002365

2

A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.

Bertolini S, Pisciotta L, Seri M, Cusano R, Cantafora A, Calabresi L, Franceschini G, Ravazzolo R, Calandra S. Bertolini S, et al. Among authors: calabresi l. Atherosclerosis. 2001 Feb 15;154(3):599-605. doi: 10.1016/s0021-9150(00)00587-6. Atherosclerosis. 2001. PMID: 11257260

3

The C-terminal domain of apolipoprotein A-I is involved in ABCA1-driven phospholipid and cholesterol efflux.

Favari E, Bernini F, Tarugi P, Franceschini G, Calabresi L. Favari E, et al. Among authors: calabresi l. Biochem Biophys Res Commun. 2002 Dec 20;299(5):801-5. doi: 10.1016/s0006-291x(02)02745-6. Biochem Biophys Res Commun. 2002. PMID: 12470649

4

Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2 +5G>C mutation in ABCA1 gene.

Altilia S, Pisciotta L, Garuti R, Tarugi P, Cantafora A, Calabresi L, Tagliabue J, Maccari S, Bernini F, Zanotti I, Vergani C, Bertolini S, Calandra S. Altilia S, et al. Among authors: calabresi l. J Lipid Res. 2003 Feb;44(2):254-64. doi: 10.1194/jlr.M200248-JLR200. Epub 2002 Nov 4. J Lipid Res. 2003. PMID: 12576507 Free article.

5

Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency.

Pisciotta L, Miccoli R, Cantafora A, Calabresi L, Tarugi P, Alessandrini P, Bittolo Bon G, Franceschini G, Cortese C, Calandra S, Bertolini S. Pisciotta L, et al. Among authors: calabresi l. Atherosclerosis. 2003 Apr;167(2):335-45. doi: 10.1016/s0021-9150(03)00020-0. Atherosclerosis. 2003. PMID: 12818417

6

Depletion of pre-beta-high density lipoprotein by human chymase impairs ATP-binding cassette transporter A1- but not scavenger receptor class B type I-mediated lipid efflux to high density lipoprotein.

Favari E, Lee M, Calabresi L, Franceschini G, Zimetti F, Bernini F, Kovanen PT. Favari E, et al. Among authors: calabresi l. J Biol Chem. 2004 Mar 12;279(11):9930-6. doi: 10.1074/jbc.M312476200. Epub 2003 Dec 29. J Biol Chem. 2004. PMID: 14701812 Free article.

7

A 33-year-old man with nephrotic syndrome and lecithin-cholesterol acyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT gene.

Frascà GM, Soverini L, Tampieri E, Franceschini G, Calabresi L, Pisciotta L, Preda P, Vangelista A, Stefoni S, Bertolini S. Frascà GM, et al. Among authors: calabresi l. Nephrol Dial Transplant. 2004 Jun;19(6):1622-4. doi: 10.1093/ndt/gfh179. Nephrol Dial Transplant. 2004. PMID: 15150357 No abstract available.

8

Effect of statins on LDL particle size in patients with familial combined hyperlipidemia: a comparison between atorvastatin and pravastatin.

Sirtori CR, Calabresi L, Pisciotta L, Cattin L, Pauciullo P, Montagnani M, Manzato E, Bittolo Bon G, Fellin R. Sirtori CR, et al. Among authors: calabresi l. Nutr Metab Cardiovasc Dis. 2005 Feb;15(1):47-55. doi: 10.1016/j.numecd.2004.08.001. Nutr Metab Cardiovasc Dis. 2005. PMID: 15871851 Clinical Trial.

9

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, 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 S, Franceschini G. Calabresi L, et al. Arterioscler Thromb Vasc Biol. 2005 Sep;25(9):1972-8. doi: 10.1161/01.ATV.0000175751.30616.13. Epub 2005 Jun 30. Arterioscler Thromb Vasc Biol. 2005. PMID: 15994445

10

Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes.

Pisciotta L, Calabresi L, Lupattelli G, Siepi D, Mannarino MR, Moleri E, Bellocchio A, Cantafora A, Tarugi P, Calandra S, Bertolini S. Pisciotta L, et al. Among authors: calabresi l. Atherosclerosis. 2005 Sep;182(1):153-9. doi: 10.1016/j.atherosclerosis.2005.01.048. Epub 2005 Mar 31. Atherosclerosis. 2005. PMID: 16115486

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