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ANGPTL3 Deficiency and Risk of Hepatic Steatosis.
D'Erasmo L, Di Martino M, Neufeld T, Fraum TJ, Kang CJ, Burks KH, Di Costanzo A, Minicocci I, Bini S, Maranghi M, Pigna G, Labbadia G, Zheng J, Fierro D, Montali A, Ceci F, Catalano C, Davidson NO, Lucisano G, Nicolucci A, Arca M, Stitziel NO. D'Erasmo L, et al. Among authors: di costanzo a. Circulation. 2023 Nov 7;148(19):1479-1489. doi: 10.1161/CIRCULATIONAHA.123.065866. Epub 2023 Sep 15. Circulation. 2023. PMID: 37712257
Autosomal recessive hypercholesterolemia: update for 2020.
D'Erasmo L, Di Costanzo A, Arca M. D'Erasmo L, et al. Among authors: di costanzo a. Curr Opin Lipidol. 2020 Apr;31(2):56-61. doi: 10.1097/MOL.0000000000000664. Curr Opin Lipidol. 2020. PMID: 32011344 Review.
Clinical Implications of Monogenic Versus Polygenic Hypercholesterolemia: Long-Term Response to Treatment, Coronary Atherosclerosis Burden, and Cardiovascular Events.
D'Erasmo L, Minicocci I, Di Costanzo A, Pigna G, Commodari D, Ceci F, Montali A, Brancato F, Stanca I, Nicolucci A, Ascione A, Galea N, Carbone I, Francone M, Maranghi M, Arca M. D'Erasmo L, et al. Among authors: di costanzo a. J Am Heart Assoc. 2021 May 4;10(9):e018932. doi: 10.1161/JAHA.120.018932. Epub 2021 Apr 23. J Am Heart Assoc. 2021. PMID: 33890476 Free PMC article.
Differential effects of bariatric surgery on plasma levels of ANGPTL3 and ANGPTL4.
Bini S, D'Erasmo L, Astiarraga B, Minicocci I, Palumbo M, Pecce V, Polito L, Di Costanzo A, Haeusler RA, Arca M, Ferrannini E, Camastra S. Bini S, et al. Among authors: di costanzo a. Nutr Metab Cardiovasc Dis. 2022 Nov;32(11):2647-2654. doi: 10.1016/j.numecd.2022.08.019. Epub 2022 Sep 1. Nutr Metab Cardiovasc Dis. 2022. PMID: 36163215 Free PMC article.
How ANGPTL3 Inhibition Will Help Our Clinical Practice?
Bini S, Tramontano D, Minicocci I, Di Costanzo A, Tambaro F, D'Erasmo L, Arca M. Bini S, et al. Among authors: di costanzo a. Curr Atheroscler Rep. 2023 Jan;25(1):19-29. doi: 10.1007/s11883-022-01076-w. Epub 2023 Jan 6. Curr Atheroscler Rep. 2023. PMID: 36607583 Review.
Contribution of mutations in low density lipoprotein receptor (LDLR) and lipoprotein lipase (LPL) genes to familial combined hyperlipidemia (FCHL): a reappraisal by using a resequencing approach.
Minicocci I, Prisco C, Montali A, Di Costanzo A, Ceci F, Pigna G, Arca M. Minicocci I, et al. Among authors: di costanzo a. Atherosclerosis. 2015 Oct;242(2):618-24. doi: 10.1016/j.atherosclerosis.2015.06.036. Epub 2015 Jun 18. Atherosclerosis. 2015. PMID: 26342331
211 results