Tavazzi D - Search Results

1

UGT1A1 genotype does not affect tyrosine kinase inhibitors efficacy and safety in chronic myeloid leukemia.

Iurlo A, Bucelli C, Cattaneo D, Levati GV, Viani B, Tavazzi D, Consonni D, Baldini L, Cappellini MD. Iurlo A, et al. Among authors: tavazzi d. Am J Hematol. 2019 Nov;94(11):E283-E285. doi: 10.1002/ajh.25596. Epub 2019 Aug 9. Am J Hematol. 2019. PMID: 31364196 Free article. No abstract available.

2

Circulating cell-free DNA and ineffective erythropoiesis in nontransfusion-dependent β-thalassemia.

Tavazzi D, Motta I, Graziadei G, Sampietro M, Duca L, Cappellini MD. Tavazzi D, et al. Am J Hematol. 2018 Nov;93(11):E365-E368. doi: 10.1002/ajh.25248. Epub 2018 Sep 9. Am J Hematol. 2018. PMID: 30105870 Free article. No abstract available.

3

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.

4

Red blood cell enzyme disorders: an overview.

Tavazzi D, Taher A, Cappellini MD. Tavazzi D, et al. Pediatr Ann. 2008 May;37(5):303-10. doi: 10.3928/00904481-20080501-08. Pediatr Ann. 2008. PMID: 18543541 Review. No abstract available.

5

Gene symbol: G6PD. Disease: Glucose-6-phosphate dehydrogenase deficiency.

Delbini P, Duca L, Nava I, Tavazzi D, Cappellini MD. Delbini P, et al. Among authors: tavazzi d. Hum Genet. 2008 Oct;124(3):312-3. Hum Genet. 2008. PMID: 18846656 No abstract available.

6

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.

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. 2012 Oct 15-Dec 15;49(3-4):147-51. doi: 10.1016/j.bcmd.2012.06.002. Epub 2012 Jun 29. Blood Cells Mol Dis. 2012. PMID: 22748422

7

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.

8

Iron status and HFE genotype in erythrocyte pyruvate kinase deficiency: study of Italian cases.

Zanella A, Bianchi P, Iurlo A, Boschetti C, Taioli E, Vercellati C, Zappa M, Fermo E, Tavazzi D, Sampietro M. Zanella A, et al. Among authors: tavazzi d. Blood Cells Mol Dis. 2001 May-Jun;27(3):653-61. doi: 10.1006/bcmd.2001.0433. Blood Cells Mol Dis. 2001. PMID: 11482880

9

Levels of uroporphyrinogen decarboxylase (URO-D) in erythrocytes of Italian porphyria cutanea tarda patients.

Tavazzi D, Martinez di Montemuros F, Fargion S, Fracanzani AL, Fiorelli G, Cappellini MD. Tavazzi D, et al. Cell Mol Biol (Noisy-le-grand). 2002 Feb;48(1):27-32. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 11929044

10

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

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