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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
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2024 9
2025 0

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132 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.
Dietary supplements in neurological diseases and brain aging.
Naureen Z, Dhuli K, Medori MC, Caruso P, Manganotti P, Chiurazzi P, Bertelli M. Naureen Z, et al. Among authors: chiurazzi p. J Prev Med Hyg. 2022 Oct 17;63(2 Suppl 3):E174-E188. doi: 10.15167/2421-4248/jpmh2022.63.2S3.2759. eCollection 2022 Jun. J Prev Med Hyg. 2022. PMID: 36479494 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.
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.
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.
Scala M, Nishikawa M, Ito H, Tabata H, Khan T, Accogli A, Davids L, Ruiz A, Chiurazzi P, Cericola G, Schulte B, Monaghan KG, Begtrup A, Torella A, Pinelli M, Denommé-Pichon AS, Vitobello A, Racine C, Mancardi MM, Kiss C, Guerin A, Wu W, Gabau Vila E, Mak BC, Martinez-Agosto JA, Gorin MB, Duz B, Bayram Y, Carvalho CMB, Vengoechea JE, Chitayat D, Tan TY, Callewaert B, Kruse B, Bird LM, Faivre L, Zollino M, Biskup S; Undiagnosed Diseases Network; Telethon Undiagnosed Diseases Program; Striano P, Nigro V, Severino M, Capra V, Costain G, Nagata KI. Scala M, et al. Among authors: chiurazzi p. Brain. 2022 Sep 14;145(9):3308-3327. doi: 10.1093/brain/awac106. Brain. 2022. PMID: 35851598 Free PMC article.
AKR1C1 and hormone metabolism in lipedema pathogenesis: a computational biology approach.
Kaftalli J, Bonetti G, Marceddu G, Dhuli K, Maltese PE, Donato K, Herbst KL, Michelini S, Chiurazzi P, Hill M, Michelini S, Michelini S, Bernini A, Bertelli M. Kaftalli J, et al. Among authors: chiurazzi p. Eur Rev Med Pharmacol Sci. 2023 Dec;27(6 Suppl):137-147. doi: 10.26355/eurrev_202312_34698. Eur Rev Med Pharmacol Sci. 2023. PMID: 38112954 Free 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.
132 results