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

Year Number of Results
2002 2
2003 1
2004 4
2005 4
2006 1
2007 4
2008 5
2010 1
2011 3
2012 3
2013 2
2014 1
2015 2
2016 4
2019 4
2020 14
2021 9
2022 12
2023 7
2024 3

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79 results

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Page 1
A novel homozygous splice site variant in ARL2BP causes a syndromic autosomal recessive rod-cone dystrophy with situs inversus, asthenozoospermia, unilateral renal agenesis and microcysts.
Placidi G, D'Agostino E, Maltese PE, Savastano MC, Gambini G, Rizzo S, Bonetti G, Bertelli M, Chiurazzi P, Falsini B. Placidi G, et al. Among authors: chiurazzi p. BMC Med Genomics. 2024 Apr 22;17(1):100. doi: 10.1186/s12920-024-01868-w. BMC Med Genomics. 2024. PMID: 38649918 Free PMC article.
Pathogenic variants in SOX11 mimicking Pitt-Hopkins syndrome phenotype.
Pasquetti D, L'Erario FF, Marangi G, Panfili A, Chiurazzi P, Sonnini E, Orteschi D, Alfieri P; TUDP Study Group; Morleo M, Nigro V, Zollino M. Pasquetti D, et al. Among authors: chiurazzi p. Clin Genet. 2024 Jan;105(1):81-86. doi: 10.1111/cge.14414. Epub 2023 Aug 9. Clin Genet. 2024. PMID: 37558216
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.
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.
79 results