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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2013 1
2015 2
2016 7
2017 7
2018 6
2019 10
2020 7
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36 results
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Page 1
Molecular foundations of chiropractic therapy.
Maltese PE, Michelini S, Baronio M, Bertelli M. Maltese PE, et al. Acta Biomed. 2019 Sep 30;90(10-S):93-102. doi: 10.23750/abm.v90i10-S.8768. Acta Biomed. 2019. PMID: 31577263 Free PMC article. Review.
Cystic Hygroma: A Preliminary Genetic Study and a Short Review from the Literature.
Noia G, Maltese PE, Zampino G, D'Errico M, Cammalleri V, Convertini P, Marceddu G, Mueller M, Guerri G, Bertelli M. Noia G, et al. Among authors: maltese pe. Lymphat Res Biol. 2019 Feb;17(1):30-39. doi: 10.1089/lrb.2017.0084. Epub 2018 Nov 22. Lymphat Res Biol. 2019. PMID: 30475086 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. 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.
Increasing evidence of hereditary lymphedema caused by CELSR1 loss-of-function variants.
Maltese PE, Michelini S, Ricci M, Maitz S, Fiorentino A, Serrani R, Lazzerotti A, Bruson A, Paolacci S, Benedetti S, Bertelli M. Maltese PE, et al. Am J Med Genet A. 2019 Sep;179(9):1718-1724. doi: 10.1002/ajmg.a.61269. Epub 2019 Jun 18. Am J Med Genet A. 2019. PMID: 31215153
Novel USH1G homozygous variant underlying USH2-like phenotype of Usher syndrome.
D'Esposito F, Randazzo V, Cennamo G, Centore N, Maltese PE, Malesci R, D'Andrea L, Bertelli M, Marciano E, de Crecchio G, Pioppo A, Magli A, Cordeiro MF. D'Esposito F, et al. Among authors: maltese pe. Eur J Ophthalmol. 2019 Sep 30:1120672119879392. doi: 10.1177/1120672119879392. Online ahead of print. Eur J Ophthalmol. 2019. PMID: 31566003
Pathogenicity of new BEST1 variants identified in Italian patients with best vitelliform macular dystrophy assessed by computational structural biology.
Frecer V, Iarossi G, Salvetti AP, Maltese PE, Delledonne G, Oldani M, Staurenghi G, Falsini B, Minnella AM, Ziccardi L, Magli A, Colombo L, D'Esposito F, Miertus J, Viola F, Attanasio M, Maggio E, Bertelli M. Frecer V, et al. Among authors: maltese pe. J Transl Med. 2019 Oct 1;17(1):330. doi: 10.1186/s12967-019-2080-3. J Transl Med. 2019. PMID: 31570112 Free PMC article.
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: maltese pe. 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.
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: maltese pe. 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 tests for low- and middle-income countries: a literature review.
Maltese PE, Poplavskaia E, Malyutkina I, Sirocco F, Bonizzato A, Capodicasa N, Nicoulina SY, Salmina A, Aksutina N, Dundar M, Beccari T, Cecchin S, Bertelli M. Maltese PE, et al. Genet Mol Res. 2017 Feb 8;16(1). doi: 10.4238/gmr16019466. Genet Mol Res. 2017. PMID: 28198508 Review.
Multimodal Imaging in Autosomal Dominant Cone-Rod Dystrophy Caused by Novel CRX Variant.
D'Esposito F, Cennamo G, de Crecchio G, Maltese PE, Cecchin S, Bertelli M, Ziccardi L, Esposito Veneruso P, Magli A, Cennamo G, Cordeiro MF. D'Esposito F, et al. Among authors: maltese pe. Ophthalmic Res. 2018;60(3):169-175. doi: 10.1159/000489460. Epub 2018 Aug 3. Ophthalmic Res. 2018. PMID: 30078014
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