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

Year Number of Results
1979 1
1990 1
1992 1
1995 1
1999 3
2000 1
2001 1
2002 1
2003 3
2004 4
2005 4
2006 1
2007 1
2008 4
2009 2
2010 2
2011 3
2012 5
2013 2
2014 1
2015 3
2016 3
2017 1
2018 1
2021 2
2024 0

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47 results

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Page 1
Morquio B disease: From pathophysiology towards diagnosis.
Caciotti A, Cellai L, Tonin R, Mei D, Procopio E, Di Rocco M, Andaloro A, Antuzzi D, Rampazzo A, Rigoldi M, Forni G, la Marca G, Guerrini R, Morrone A. Caciotti A, et al. Among authors: antuzzi d. Mol Genet Metab. 2021 Mar;132(3):180-188. doi: 10.1016/j.ymgme.2021.01.008. Epub 2021 Feb 1. Mol Genet Metab. 2021. PMID: 33558080
Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.
Zampetti A, Orteu CH, Antuzzi D, Bongiorno MR, Manco S, Gnarra M, Morrone A, Cardinali G, Kovacs D, Aspite N, Linder D, Parini R, Feliciani C; Interdisciplinary Study Group on Fabry Disease (ISGF). Zampetti A, et al. Among authors: antuzzi d. Br J Dermatol. 2012 Apr;166(4):712-20. doi: 10.1111/j.1365-2133.2012.10742.x. Br J Dermatol. 2012. PMID: 22452439 Review.
Clinical use of plasma chitotriosidase in severe sepsis.
Chiarla C, Giovannini I, Antuzzi D, Piras A, Ardito F, Giuliante F. Chiarla C, et al. Among authors: antuzzi d. Curr Med Res Opin. 2016;32(2):273-6. doi: 10.1185/03007995.2015.1118370. Epub 2015 Dec 2. Curr Med Res Opin. 2016. PMID: 26550788
Kidney transplantation in patients with Fabry disease.
Cybulla M, Walter KN, Schwarting A, Divito R, Feriozzi S, Sunder-Plassmann G; European FOS Investigators Group. Cybulla M, et al. Transpl Int. 2009 Apr;22(4):475-81. doi: 10.1111/j.1432-2277.2008.00824.x. Epub 2009 Jan 22. Transpl Int. 2009. PMID: 19207191 Free article.
Anderson-Fabry's Disease: A Rare but Treatable Case of Fever of Unknown Origin.
Graziani F, Ruggio A, Iaconelli A, Verrecchia E, Morrone A, Antuzzi D, Crea F, Manna R. Graziani F, et al. Among authors: antuzzi d. Eur J Case Rep Intern Med. 2017 Jul 3;4(7):000645. doi: 10.12890/2017_000645. eCollection 2017. Eur J Case Rep Intern Med. 2017. PMID: 30755957 Free PMC article.
Optimizing the molecular diagnosis of GALNS: novel methods to define and characterize Morquio-A syndrome-associated mutations.
Caciotti A, Tonin R, Rigoldi M, Ferri L, Catarzi S, Cavicchi C, Procopio E, Donati MA, Ficcadenti A, Fiumara A, Barone R, Garavelli L, Rocco MD, Filocamo M, Antuzzi D, Scarpa M, Mooney SD, Li B, Skouma A, Bianca S, Concolino D, Casalone R, Monti E, Pantaleo M, Giglio S, Guerrini R, Parini R, Morrone A. Caciotti A, et al. Among authors: antuzzi d. Hum Mutat. 2015 Mar;36(3):357-68. doi: 10.1002/humu.22751. Hum Mutat. 2015. PMID: 25545067
47 results