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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. 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.
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: manara e. 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.
Sudden unexplained death due to cardiac arrest.
Precone V, Guerri G, Krasi G, Lupi L, Papa I, Beccari T, Maltese PE, Manara E, Bertelli M. Precone V, et al. Among authors: manara e. Acta Biomed. 2019 Sep 30;90(10-S):30-31. doi: 10.23750/abm.v90i10-S.8753. Acta Biomed. 2019. PMID: 31577250 Free PMC article. Review.
Genetic testing for autonomic dysfunction or dysautonomias.
Maltese PE, Manara E, Beccari T, Dundar M, Capodicasa N, Bertelli M. Maltese PE, et al. Among authors: manara e. Acta Biomed. 2020 Nov 9;91(13-S):e2020002. doi: 10.23750/abm.v91i13-S.10518. Acta Biomed. 2020. PMID: 33170169 Free PMC article. Review.
Genetic analysis of intellectual disability and autism.
Chiurazzi P, Kiani AK, Miertus J, Paolacci S, Barati S, Manara E, Stuppia L, Gurrieri F, Bertelli M. Chiurazzi P, et al. Among authors: manara e. Acta Biomed. 2020 Nov 9;91(13-S):e2020003. doi: 10.23750/abm.v91i13-S.10684. Acta Biomed. 2020. PMID: 33170170 Free PMC article. Review.
A next generation sequencing gene panel for use in the diagnosis of anorexia nervosa.
Ceccarini MR, Precone V, Manara E, Paolacci S, Maltese PE, Benfatti V, Dhuli K, Donato K, Guerri G, Marceddu G, Chiurazzi P, Dalla Ragione L, Beccari T, Bertelli M. Ceccarini MR, et al. Among authors: manara e. Eat Weight Disord. 2022 Jun;27(5):1869-1880. doi: 10.1007/s40519-021-01331-0. Epub 2021 Nov 25. Eat Weight Disord. 2022. PMID: 34822136
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: manara e. 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.
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: manara e. 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
96 results