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

Year Number of Results
2002 5
2003 2
2004 3
2005 6
2006 3
2007 5
2008 4
2009 3
2010 3
2011 4
2012 7
2013 4
2014 1
2015 2
2016 3
2017 1
2018 5
2019 3
2020 1
2022 1
2024 0

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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: galliano 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.
The extraordinary ligand binding properties of human serum albumin.
Fasano M, Curry S, Terreno E, Galliano M, Fanali G, Narciso P, Notari S, Ascenzi P. Fasano M, et al. Among authors: galliano m. IUBMB Life. 2005 Dec;57(12):787-96. doi: 10.1080/15216540500404093. IUBMB Life. 2005. PMID: 16393781 Free article. Review.
Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT).
Campagnoli M, Hansson P, Dolcini L, Caridi G, Dagnino M, Candiano G, Bruschi M, Palmqvist L, Galliano M, Minchiotti L. Campagnoli M, et al. Among authors: galliano m. Clin Chim Acta. 2008 Oct;396(1-2):89-92. doi: 10.1016/j.cca.2008.06.008. Epub 2008 Jun 12. Clin Chim Acta. 2008. PMID: 18602380
56 results