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

Year Number of Results
1992 1
1993 2
1994 4
1995 1
1996 5
1997 1
1998 1
1999 7
2000 3
2001 5
2002 2
2003 3
2004 5
2005 4
2006 2
2007 4
2008 5
2010 1
2011 4
2012 3
2013 2
2014 1
2015 2
2016 4
2019 6
2020 16
2021 11
2022 12
2023 13
2024 9
2025 6
2026 3

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141 results

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Page 1
Polymorphisms, diet and nutrigenomics.
Kiani AK, Bonetti G, Donato K, Kaftalli J, Herbst KL, Stuppia L, Fioretti F, Nodari S, Perrone M, Chiurazzi P, Bellinato F, Gisondi P, Bertelli M. Kiani AK, et al. Among authors: chiurazzi p. J Prev Med Hyg. 2022 Oct 17;63(2 Suppl 3):E125-E141. doi: 10.15167/2421-4248/jpmh2022.63.2S3.2754. eCollection 2022 Jun. J Prev Med Hyg. 2022. PMID: 36479483 Free PMC article. Review.
Cardiac conduction defects.
Guerri G, Krasi G, Precone V, Paolacci S, Chiurazzi P, Arrigoni L, Cortese B, Dautaj A, Bertelli M. Guerri G, et al. Among authors: chiurazzi p. Acta Biomed. 2019 Sep 30;90(10-S):20-29. doi: 10.23750/abm.v90i10-S.8751. Acta Biomed. 2019. PMID: 31577249 Free PMC article. Review.
Genetic Aspects of Tooth Agenesis.
Modafferi C, Tucci I, Bogliardi FM, Gimondo E, Chiurazzi P, Tabolacci E, Grippaudo C. Modafferi C, et al. Among authors: chiurazzi p. Genes (Basel). 2025 May 15;16(5):582. doi: 10.3390/genes16050582. Genes (Basel). 2025. PMID: 40428404 Free PMC article. Review.
X-linked mental retardation.
Neri G, Chiurazzi P. Neri G, et al. Among authors: chiurazzi p. Adv Genet. 1999;41:55-94. doi: 10.1016/s0065-2660(08)60151-0. Adv Genet. 1999. PMID: 10494617 Review. No abstract available.
Fragile X syndrome.
Terracciano A, Chiurazzi P, Neri G. Terracciano A, et al. Among authors: chiurazzi p. Am J Med Genet C Semin Med Genet. 2005 Aug 15;137C(1):32-7. doi: 10.1002/ajmg.c.30062. Am J Med Genet C Semin Med Genet. 2005. PMID: 16010677 Review.
Clinical-Genetic Approach to Conditions with Macrocephaly and ASD/Behaviour Abnormalities: Variants in PTEN and PPP2R5D Are the Most Recurrent Gene Mutations in a Patient-Oriented Diagnostic Strategy.
L'Erario FF, Gazzellone A, Contaldo I, Veredice C, Carapelle M, Renzi AG, Modafferi C, Palucci M, D'Ambrosio P, Sonnini E, Loberti L, Panfili A, Lucci Cordisco E, Chiurazzi P, Trevisan V, Leoni C, Zampino G, Pomponi MG, Orteschi D, Zollino M, Marangi G. L'Erario FF, et al. Among authors: chiurazzi p. Genes (Basel). 2025 Apr 20;16(4):469. doi: 10.3390/genes16040469. Genes (Basel). 2025. PMID: 40282429 Free PMC article.
Author Correction: Aldo-keto reductase 1C2 (AKR1C2) as the second gene associated to non-syndromic primary lipedema: investigating activating mutation or overexpression as causative factors.
Kaftalli J, Donato K, Bonetti G, Dhuli K, Macchia A, Maltese PE, Louise Herbst K, Michelini S, Chiurazzi P, Hill M, Michelini S, Michelini S, Marceddu G, Bernini A, Bertelli M. Kaftalli J, et al. Among authors: chiurazzi p. Eur Rev Med Pharmacol Sci. 2024 Mar;28(6):2626. doi: 10.26355/eurrev_202403_35776. Eur Rev Med Pharmacol Sci. 2024. PMID: 38567622 Free article.
XLMR genes: update 1994.
Neri G, Chiurazzi P, Arena JF, Lubs HA. Neri G, et al. Among authors: chiurazzi p. Am J Med Genet. 1994 Jul 15;51(4):542-9. doi: 10.1002/ajmg.1320510451. Am J Med Genet. 1994. PMID: 7943038 Review.
141 results