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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
Non-alcoholic fatty liver disease and subclinical atherosclerosis: A comparison of metabolically- versus genetically-driven excess fat hepatic storage.
Di Costanzo A, D'Erasmo L, Polimeni L, Baratta F, Coletta P, Di Martino M, Loffredo L, Perri L, Ceci F, Montali A, Girelli G, De Masi B, Angeloni A, Catalano C, Maranghi M, Del Ben M, Angelico F, Arca M. Di Costanzo A, et al. Among authors: di martino m. Atherosclerosis. 2017 Feb;257:232-239. doi: 10.1016/j.atherosclerosis.2016.12.018. Epub 2016 Dec 21. Atherosclerosis. 2017. PMID: 28027788
Analysis of Children and Adolescents with Familial Hypercholesterolemia.
Minicocci I, Pozzessere S, Prisco C, Montali A, di Costanzo A, Martino E, Martino F, Arca M. Minicocci I, et al. Among authors: di costanzo a. J Pediatr. 2017 Apr;183:100-107.e3. doi: 10.1016/j.jpeds.2016.12.075. Epub 2017 Feb 1. J Pediatr. 2017. PMID: 28161202
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia.
Di Costanzo A, Di Leo E, Noto D, Cefalù AB, Minicocci I, Polito L, D'Erasmo L, Cantisani V, Spina R, Tarugi P, Averna M, Arca M. Di Costanzo A, et al. Among authors: di leo e. J Clin Lipidol. 2017 Sep-Oct;11(5):1234-1242. doi: 10.1016/j.jacl.2017.06.013. Epub 2017 Jun 24. J Clin Lipidol. 2017. PMID: 28733173
PNPLA3 variant and portal/periportal histological pattern in patients with biopsy-proven non-alcoholic fatty liver disease: a possible role for oxidative stress.
Carpino G, Pastori D, Baratta F, Overi D, Labbadia G, Polimeni L, Di Costanzo A, Pannitteri G, Carnevale R, Del Ben M, Arca M, Violi F, Angelico F, Gaudio E. Carpino G, et al. Among authors: di costanzo a. Sci Rep. 2017 Nov 17;7(1):15756. doi: 10.1038/s41598-017-15943-z. Sci Rep. 2017. PMID: 29150621 Free PMC article.
Evaluation of Polygenic Determinants of Non-Alcoholic Fatty Liver Disease (NAFLD) By a Candidate Genes Resequencing Strategy.
Di Costanzo A, Belardinilli F, Bailetti D, Sponziello M, D'Erasmo L, Polimeni L, Baratta F, Pastori D, Ceci F, Montali A, Girelli G, De Masi B, Angeloni A, Giannini G, Del Ben M, Angelico F, Arca M. Di Costanzo A, et al. Sci Rep. 2018 Feb 27;8(1):3702. doi: 10.1038/s41598-018-21939-0. Sci Rep. 2018. PMID: 29487372 Free PMC article.
Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an "FCS score".
Moulin P, Dufour R, Averna M, Arca M, Cefalù AB, Noto D, D'Erasmo L, Di Costanzo A, Marçais C, Alvarez-Sala Walther LA, Banach M, Borén J, Cramb R, Gouni-Berthold I, Hughes E, Johnson C, Pintó X, Reiner Ž, van Lennep JR, Soran H, Stefanutti C, Stroes E, Bruckert E. Moulin P, et al. Among authors: di costanzo a. Atherosclerosis. 2018 Aug;275:265-272. doi: 10.1016/j.atherosclerosis.2018.06.814. Epub 2018 Jun 18. Atherosclerosis. 2018. PMID: 29980054 Free article. Review.
Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score.
Moulin P, Dufour R, Averna M, Arca M, Cefalù AB, Noto D, D'Erasmo L, Di Costanzo A, Marçais C, Walther LAA, Banach M, Borén J, Cramb R, Gouni-Berthold I, Hughes E, Johnson C, Pintó X, Reiner Ž, van Lennep JR, Soran H, Stefanutti C, Stroes E, Bruckert E. Moulin P, et al. Among authors: di costanzo a. Data Brief. 2018 Oct 27;21:1334-1336. doi: 10.1016/j.dib.2018.10.125. eCollection 2018 Dec. Data Brief. 2018. PMID: 30456254 Free PMC article.
217 results