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Genetic tests in lymphatic vascular malformations and lymphedema.
Michelini S, Paolacci S, Manara E, Eretta C, Mattassi R, Lee BB, Bertelli M. Michelini S, et al. Among authors: bertelli m. J Med Genet. 2018 Apr;55(4):222-232. doi: 10.1136/jmedgenet-2017-105064. Epub 2018 Feb 9. J Med Genet. 2018. PMID: 29440349
Mendelian obesity, molecular pathways and pharmacological therapies: a review.
Paolacci S, Borrelli A, Stuppia L, Campanile FC, Dallavilla T, Krajčovič J, Veselenyiova D, Beccari T, Unfer V, Bertelli M; Geneob Project. Paolacci S, et al. Among authors: bertelli m. Eur Rev Med Pharmacol Sci. 2019 Feb;23(3):1357-1378. doi: 10.26355/eurrev_201902_17031. Eur Rev Med Pharmacol Sci. 2019. PMID: 30779104 Free article. Review.
Taste, olfactory and texture related genes and food choices: implications on health status.
Precone V, Beccari T, Stuppia L, Baglivo M, Paolacci S, Manara E, Miggiano GAD, Falsini B, Trifirò A, Zanlari A, Herbst KL, Unfer V, Bertelli M; Geneob Project. Precone V, et al. Among authors: bertelli m. Eur Rev Med Pharmacol Sci. 2019 Feb;23(3):1305-1321. doi: 10.26355/eurrev_201902_17026. Eur Rev Med Pharmacol Sci. 2019. PMID: 30779105 Free article. Review.
Vascular anomalies: molecular bases, genetic testing and therapeutic approaches.
Paolacci S, Zulian A, Bruson A, Manara E, Michelini S, Mattassi RE, Lee BB, Amato B, Bertelli M. Paolacci S, et al. Among authors: bertelli m. Int Angiol. 2019 Apr;38(2):157-170. doi: 10.23736/S0392-9590.19.04154-3. Epub 2019 Apr 1. Int Angiol. 2019. PMID: 30938497 Free article. Review.
Mutation profile of BBS genes in patients with Bardet-Biedl syndrome: an Italian study.
Manara E, Paolacci S, D'Esposito F, Abeshi A, Ziccardi L, Falsini B, Colombo L, Iarossi G, Pilotta A, Boccone L, Guerri G, Monica M, Marta B, Maltese PE, Buzzonetti L, Rossetti L, Bertelli M. Manara E, et al. Among authors: bertelli m. Ital J Pediatr. 2019 Jun 13;45(1):72. doi: 10.1186/s13052-019-0659-1. Ital J Pediatr. 2019. PMID: 31196119 Free PMC article.
Genetics of lipedema: new perspectives on genetic research and molecular diagnoses.
Paolacci S, Precone V, Acquaviva F, Chiurazzi P, Fulcheri E, Pinelli M, Buffelli F, Michelini S, Herbst KL, Unfer V, Bertelli M; GeneOb Project. Paolacci S, et al. Among authors: bertelli m. Eur Rev Med Pharmacol Sci. 2019 Jul;23(13):5581-5594. doi: 10.26355/eurrev_201907_18292. Eur Rev Med Pharmacol Sci. 2019. PMID: 31298310 Free article. Review.
Putative role of Brugada syndrome genes in familial atrial fibrillation.
Maltese PE, Aldanova E, Kriuchkova N, Averianov A, Manara E, Paolacci S, Bruson A, Miotto R, Sartori M, Guerri G, Zuntini M, Marceddu G, Tezzele S, Tadtaeva K, Chernova A, Aksyutina N, Nikulina S, Nodari S, Bertelli M. Maltese PE, et al. Among authors: bertelli m. Eur Rev Med Pharmacol Sci. 2019 Sep;23(17):7582-7598. doi: 10.26355/eurrev_201909_18880. Eur Rev Med Pharmacol Sci. 2019. PMID: 31539150 Free article.
391 results