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Laboratory Diagnosis of Porphyria.
Di Pierro E, De Canio M, Mercadante R, Savino M, Granata F, Tavazzi D, Nicolli AM, Trevisan A, Marchini S, Fustinoni S. Di Pierro E, et al. Among authors: tavazzi d. Diagnostics (Basel). 2021 Jul 26;11(8):1343. doi: 10.3390/diagnostics11081343. Diagnostics (Basel). 2021. PMID: 34441276 Free PMC article. Review.
Porphyrias at a glance: diagnosis and treatment.
Cappellini MD, Brancaleoni V, Graziadei G, Tavazzi D, Di Pierro E. Cappellini MD, et al. Among authors: tavazzi d. Intern Emerg Med. 2010 Oct;5 Suppl 1:S73-80. doi: 10.1007/s11739-010-0449-7. Intern Emerg Med. 2010. PMID: 20865478 Review.
Corrigendum to "Seven novel genetic mutations within the 5' UTR and the housekeeping promoter of HMBS gene responsible for the non-erythroid form of acute intermittent porphyria" [Blood Cells Mol. Dis. 49 (2012) 147-151].
Brancaleoni V, Granata F, Colancecco A, Tavazzi D, Cappellini MD, Di Pierro E. Brancaleoni V, et al. Among authors: tavazzi d. Blood Cells Mol Dis. 2016 Nov;62:67. doi: 10.1016/j.bcmd.2016.09.001. Epub 2016 Sep 29. Blood Cells Mol Dis. 2016. PMID: 27693411 No abstract available.
A large deletion on chromosome 11 in acute intermittent porphyria.
Di Pierro E, Besana V, Moriondo V, Brancaleoni V, Tavazzi D, Casalgrandi G, Ventura P, Rocchi E, Cappellini MD. Di Pierro E, et al. Among authors: tavazzi d. Blood Cells Mol Dis. 2006 Jul-Aug;37(1):50-4. doi: 10.1016/j.bcmd.2006.05.003. Epub 2006 Jul 7. Blood Cells Mol Dis. 2006. PMID: 16828319
Molecular characterization of porphyrias in Italy: a diagnostic flow-chart.
Martinez di Montemuros F, Di Pierro E, Patti E, Tavazzi D, Danielli MG, Biolcati G, Rocchi E, Cappellini MD. Martinez di Montemuros F, et al. Among authors: tavazzi d. Cell Mol Biol (Noisy-le-grand). 2002 Dec;48(8):867-76. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 12699245
41 results