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

Year Number of Results
2011 2
2012 7
2013 2
2014 4
2015 5
2016 4
2017 1
2018 2
2020 1
2021 4
2023 1
2024 0

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30 results

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Page 1
Database tools in genetic diseases research.
Bianco AM, Marcuzzi A, Zanin V, Girardelli M, Vuch J, Crovella S. Bianco AM, et al. Among authors: girardelli m. Genomics. 2013 Feb;101(2):75-85. doi: 10.1016/j.ygeno.2012.11.001. Epub 2012 Nov 10. Genomics. 2013. PMID: 23147677 Free article. Review.
Putative modifier genes in mevalonate kinase deficiency.
Marcuzzi A, Vozzi D, Girardelli M, Tricarico PM, Knowles A, Crovella S, Vuch J, Tommasini A, Piscianz E, Bianco AM. Marcuzzi A, et al. Among authors: girardelli m. Mol Med Rep. 2016 Apr;13(4):3181-9. doi: 10.3892/mmr.2016.4918. Epub 2016 Feb 22. Mol Med Rep. 2016. PMID: 26935981
Novel NOD2 Mutation in Early-Onset Inflammatory Bowel Phenotype.
Girardelli M, Loganes C, Pin A, Stacul E, Decleva E, Vozzi D, Baj G, De Giacomo C, Tommasini A, Bianco AM. Girardelli M, et al. Inflamm Bowel Dis. 2018 May 18;24(6):1204-1212. doi: 10.1093/ibd/izy061. Inflamm Bowel Dis. 2018. PMID: 29697845
Mevalonate kinase deficiency and IBD: shared genetic background.
Bianco AM, Girardelli M, Vozzi D, Crovella S, Kleiner G, Marcuzzi A. Bianco AM, et al. Among authors: girardelli m. Gut. 2014 Aug;63(8):1367-8. doi: 10.1136/gutjnl-2013-306555. Epub 2014 Feb 14. Gut. 2014. PMID: 24531851 Free PMC article. No abstract available.
30 results