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

Year Number of Results
2014 1
2015 1
2017 3
2018 6
2019 18
2020 16
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40 results
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Page 1
Genetic syndromes with localized subcutaneous fat tissue accumulation.
Precone V, Barati S, Paolacci S, Salgarello M, Visconti G, Gentileschi S, Guerri G, Gagliardi L, Aquilanti B, Matera G, Velluti V, Miggiano GAD, Herbst KL, Bertelli M. Precone V, et al. Among authors: paolacci s. Acta Biomed. 2019 Sep 30;90(10-S):90-92. doi: 10.23750/abm.v90i10-S.8767. Acta Biomed. 2019. PMID: 31577262 Free PMC article. Review.
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. 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.
Mendelian non-syndromic obesity.
Paolacci S, Pompucci G, Paolini B, Del Ciondolo I, Miggiano GAD, Aquilanti B, Scaramuzza A, Velluti V, Matera G, Gagliardi L, Bertelli M. Paolacci S, et al. Acta Biomed. 2019 Sep 30;90(10-S):87-89. doi: 10.23750/abm.v90i10-S.8766. Acta Biomed. 2019. PMID: 31577261 Free PMC article. Review.
Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein-Taybi syndrome.
Menke LA; DDD study, Gardeitchik T, Hammond P, Heimdal KR, Houge G, Hufnagel SB, Ji J, Johansson S, Kant SG, Kinning E, Leon EL, Newbury-Ecob R, Paolacci S, Pfundt R, Ragge NK, Rinne T, Ruivenkamp C, Saitta SC, Sun Y, Tartaglia M, Terhal PA, van Essen AJ, Vigeland MD, Xiao B, Hennekam RC. Menke LA, et al. Among authors: paolacci s. Am J Med Genet A. 2018 Apr;176(4):862-876. doi: 10.1002/ajmg.a.38626. Epub 2018 Feb 20. Am J Med Genet A. 2018. PMID: 29460469
Hydroxytyrosol: A natural compound with promising pharmacological activities.
Bertelli M, Kiani AK, Paolacci S, Manara E, Kurti D, Dhuli K, Bushati V, Miertus J, Pangallo D, Baglivo M, Beccari T, Michelini S. Bertelli M, et al. Among authors: paolacci s. J Biotechnol. 2020 Feb 10;309:29-33. doi: 10.1016/j.jbiotec.2019.12.016. Epub 2019 Dec 26. J Biotechnol. 2020. PMID: 31884046 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: paolacci s. 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: paolacci s. 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
Combined use of medically-assisted reproductive techniques: a new bioethical issue.
Bertelli M, Paolacci S, Placidi G, Scaccia G, Chiurazzi P, Fulcheri E, Malacarne D, Lichterman B, Petralia P. Bertelli M, et al. Among authors: paolacci s. Acta Biomed. 2019 Sep 30;90(10-S):58-61. doi: 10.23750/abm.v90i10-S.8761. Acta Biomed. 2019. PMID: 31577256 Free PMC article. Review.
Genetics and pharmacogenetics in the diagnosis and therapy of cardiovascular diseases.
Krasi G, Precone V, Paolacci S, Stuppia L, Nodari S, Romeo F, Perrone M, Bushati V, Dautaj A, Bertelli M. Krasi G, et al. Among authors: paolacci s. Acta Biomed. 2019 Sep 30;90(10-S):7-19. doi: 10.23750/abm.v90i10-S.8748. Acta Biomed. 2019. PMID: 31577248 Free PMC article. Review.
Specific combinations of biallelic POLR3A variants cause Wiedemann-Rautenstrauch syndrome.
Paolacci S, Li Y, Agolini E, Bellacchio E, Arboleda-Bustos CE, Carrero D, Bertola D, Al-Gazali L, Alders M, Altmüller J, Arboleda G, Beleggia F, Bruselles A, Ciolfi A, Gillessen-Kaesbach G, Krieg T, Mohammed S, Müller C, Novelli A, Ortega J, Sandoval A, Velasco G, Yigit G, Arboleda H, Lopez-Otin C, Wollnik B, Tartaglia M, Hennekam RC. Paolacci S, et al. J Med Genet. 2018 Dec;55(12):837-846. doi: 10.1136/jmedgenet-2018-105528. Epub 2018 Oct 15. J Med Genet. 2018. PMID: 30323018
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