Fermo E - Search Results

1

Imatinib and ruxolitinib association: first experience in two patients.

Iurlo A, Gianelli U, Rapezzi D, Cattaneo D, Fermo E, Binda F, Santambrogio E, Bucelli C, Cortelezzi A. Iurlo A, et al. Among authors: fermo e. Haematologica. 2014 Jun;99(6):e76-7. doi: 10.3324/haematol.2013.102525. Epub 2014 Mar 14. Haematologica. 2014. PMID: 24633869 Free PMC article. No abstract available.

2

Biological and molecular characterization of PNH-like lymphocytes emerging after Campath-1H therapy.

Fracchiolla NS, Barcellini W, Bianchi P, Motta M, Fermo E, Cortelezzi A. Fracchiolla NS, et al. Among authors: fermo e. Br J Haematol. 2001 Mar;112(4):969-71. doi: 10.1046/j.1365-2141.2001.02677.x. Br J Haematol. 2001. PMID: 11298593 Free article.

3

Molecular characterization of the PK-LR gene in sixteen pyruvate kinase-deficient patients.

Zanella A, Bianchi P, Fermo E, Iurlo A, Zappa M, Vercellati C, Boschetti C, Baronciani L, Cotton F. Zanella A, et al. Among authors: fermo e. Br J Haematol. 2001 Apr;113(1):43-8. doi: 10.1046/j.1365-2141.2001.02711.x. Br J Haematol. 2001. PMID: 11328279 Free article.

4

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: fermo e. Blood Cells Mol Dis. 2001 May-Jun;27(3):653-61. doi: 10.1006/bcmd.2001.0433. Blood Cells Mol Dis. 2001. PMID: 11482880

5

Immunoregulatory cytokine polymorphisms in Italian patients affected by paroxysmal nocturnal haemoglobinuria and aplastic anaemia.

Fermo E, Bianchi P, Barcellini W, Pedotti P, Boschetti C, Alfinito F, Cortelezzi A, Zanella A. Fermo E, et al. Eur J Immunogenet. 2004 Dec;31(6):267-9. doi: 10.1111/j.1365-2370.2004.00480.x. Eur J Immunogenet. 2004. PMID: 15548264

6

VEGF expression correlates with microvessel density in Philadelphia chromosome-negative chronic myeloproliferative disorders.

Gianelli U, Vener C, Raviele PR, Savi F, Somalvico F, Calori R, Iurlo A, Radaelli F, Fermo E, Bucciarelli P, Bori S, Coggi G, Deliliers GL. Gianelli U, et al. Among authors: fermo e. Am J Clin Pathol. 2007 Dec;128(6):966-73. doi: 10.1309/FP0N3LC8MBJUFFA6. Am J Clin Pathol. 2007. PMID: 18024322

7

The significance of bone marrow biopsy and JAK2V617F mutation in the differential diagnosis between the "early" prepolycythemic phase of polycythemia vera and essential thrombocythemia.

Gianelli U, Iurlo A, Vener C, Moro A, Fermo E, Bianchi P, Graziani D, Radaelli F, Coggi G, Bosari S, Deliliers GL, Zanella A. Gianelli U, et al. Among authors: fermo e. Am J Clin Pathol. 2008 Sep;130(3):336-42. doi: 10.1309/6BQ5K8LHVYAKUAF4. Am J Clin Pathol. 2008. PMID: 18701405

8

Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.

Bianchi P, Fermo E, Vercellati C, Boschetti C, Barcellini W, Iurlo A, Marcello AP, Righetti PG, Zanella A. Bianchi P, et al. Among authors: fermo e. Hum Mutat. 2009 Sep;30(9):1292-8. doi: 10.1002/humu.21077. Hum Mutat. 2009. PMID: 19621418

9

Oxidative stress is increased in primary and post-polycythemia vera myelofibrosis.

Vener C, Novembrino C, Catena FB, Fracchiolla NS, Gianelli U, Savi F, Radaelli F, Fermo E, Cortelezzi A, Lonati S, Menegatti M, Deliliers GL. Vener C, et al. Among authors: fermo e. Exp Hematol. 2010 Nov;38(11):1058-65. doi: 10.1016/j.exphem.2010.07.005. Epub 2010 Jul 22. Exp Hematol. 2010. PMID: 20655352 Free article.

10

Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.

Bianchi P, Fermo E, Vercellati C, Marcello AP, Porretti L, Cortelezzi A, Barcellini W, Zanella A. Bianchi P, et al. Among authors: fermo e. Haematologica. 2012 Apr;97(4):516-23. doi: 10.3324/haematol.2011.052845. Epub 2011 Nov 4. Haematologica. 2012. PMID: 22058213 Free PMC article.

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