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Mutations in the ANGPTL3 gene and familial combined hypolipidemia: a clinical and biochemical characterization.
Minicocci I, Montali A, Robciuc MR, Quagliarini F, Censi V, Labbadia G, Gabiati C, Pigna G, Sepe ML, Pannozzo F, Lütjohann D, Fazio S, Jauhiainen M, Ehnholm C, Arca M. Minicocci I, et al. Among authors: arca m. J Clin Endocrinol Metab. 2012 Jul;97(7):E1266-75. doi: 10.1210/jc.2012-1298. Epub 2012 Jun 1. J Clin Endocrinol Metab. 2012. PMID: 22659251 Free PMC article.
Autosomal recessive hypercholesterolemia: update for 2020.
D'Erasmo L, Di Costanzo A, Arca M. D'Erasmo L, et al. Among authors: arca m. Curr Opin Lipidol. 2020 Apr;31(2):56-61. doi: 10.1097/MOL.0000000000000664. Curr Opin Lipidol. 2020. PMID: 32011344 Review.
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: arca m. 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
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study.
Casula M, Olmastroni E, Pirillo A, Catapano AL; MEMBERS OF THE LIPIGEN STEERING COMMETTEE; PRINCIPAL INVESTIGATORS: Coordinator center; Participant Centers; Participant Laboratories; COLLABORATORS; STUDY CENTRAL LABORATORY AND ANALYSIS GROUP. Casula M, et al. Atherosclerosis. 2018 Oct;277:413-418. doi: 10.1016/j.atherosclerosis.2018.08.013. Atherosclerosis. 2018. PMID: 30270079 Free article.
505 results