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

Year Number of Results
2002 2
2003 2
2004 2
2005 4
2006 2
2007 3
2008 2
2009 3
2010 2
2011 2
2012 4
2013 1
2014 1
2015 1
2016 2
2018 3
2019 3
2020 1
2022 1
2023 1
2024 0

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35 results

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Page 1
Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.
Minchiotti L, Caridi G, Campagnoli M, Lugani F, Galliano M, Kragh-Hansen U. Minchiotti L, et al. Among authors: campagnoli m. Front Genet. 2019 Apr 17;10:336. doi: 10.3389/fgene.2019.00336. eCollection 2019. Front Genet. 2019. PMID: 31057599 Free PMC article. Review.
Could the Oxidation of α1-Antitrypsin Prevent the Binding of Human Neutrophil Elastase in COVID-19 Patients?
D'Amato M, Campagnoli M, Iadarola P, Bignami PM, Fumagalli M, Chiarelli LR, Stelitano G, Meloni F, Linciano P, Collina S, Pietrocola G, Vertui V, Aliberti A, Fossali T, Viglio S. D'Amato M, et al. Among authors: campagnoli m. Int J Mol Sci. 2023 Aug 31;24(17):13533. doi: 10.3390/ijms241713533. Int J Mol Sci. 2023. PMID: 37686340 Free PMC article.
Recurrent Hypoglycemia in a Case of Congenital Analbuminemia.
Litzel M, Caridi G, Lugani F, Campagnoli M, Minchiotti L, Fischli S. Litzel M, et al. Among authors: campagnoli m. Case Rep Endocrinol. 2020 Feb 27;2020:8452564. doi: 10.1155/2020/8452564. eCollection 2020. Case Rep Endocrinol. 2020. PMID: 32181025 Free PMC article.
Analbuminemia produced by a novel splicing mutation.
Dolcini L, Caridi G, Dagnino M, Sala A, Gökçe S, Sökücü S, Campagnoli M, Galliano M, Minchiotti L. Dolcini L, et al. Among authors: campagnoli m. Clin Chem. 2007 Aug;53(8):1549-52. doi: 10.1373/clinchem.2007.089748. Clin Chem. 2007. PMID: 17644793
35 results