Cappellini MD - 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: cappellini md. 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

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. Among authors: cappellini md. Cell Mol Biol (Noisy-le-grand). 2002 Feb;48(1):27-32. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 11929044

3

Unusual severe development of common B lymphoblastic leukemia in Gaucher disease type I.

Castelli R, Cassinerio E, Iurlo A, Zanella A, Gianelli U, Cappellini MD. Castelli R, et al. Among authors: cappellini md. Am J Hematol. 2006 May;81(5):383-4. doi: 10.1002/ajh.20579. Am J Hematol. 2006. PMID: 16628727 Free article. No abstract available.

4

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: cappellini md. 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

5

Red blood cell enzyme disorders: an overview.

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

6

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: cappellini md. Hum Genet. 2008 Oct;124(3):312-3. Hum Genet. 2008. PMID: 18846656 No abstract available.

7

Porphyrias at a glance: diagnosis and treatment.

Cappellini MD, Brancaleoni V, Graziadei G, Tavazzi D, Di Pierro E. Cappellini MD, et al. Intern Emerg Med. 2010 Oct;5 Suppl 1:S73-80. doi: 10.1007/s11739-010-0449-7. Intern Emerg Med. 2010. PMID: 20865478 Review.

8

Epidemiology of Clostridium difficile-associated disease in internal medicine wards in northern Italy.

Mellace L, Consonni D, Jacchetti G, Del Medico M, Colombo R, Velati M, Formica S, Cappellini MD, Castaldi S, Fabio G. Mellace L, et al. Among authors: cappellini md. Intern Emerg Med. 2013 Dec;8(8):717-23. doi: 10.1007/s11739-012-0752-6. Epub 2012 Jan 17. Intern Emerg Med. 2013. PMID: 22249916

9

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: cappellini md. 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

10

The role of TMPRSS6 polymorphisms in iron deficiency anemia partially responsive to oral iron treatment.

Poggiali E, Andreozzi F, Nava I, Consonni D, Graziadei G, Cappellini MD. Poggiali E, et al. Among authors: cappellini md. Am J Hematol. 2015 Apr;90(4):306-9. doi: 10.1002/ajh.23929. Epub 2015 Mar 2. Am J Hematol. 2015. PMID: 25557470 Free article.

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