Boschetti C - Search Results

1

Intracytoplasmic hemozoin (malarial pigment) in a case of severe, aparasitemic Plasmodium falciparum malaria.

Grande R, Boschetti C. Grande R, et al. Among authors: boschetti c. Am J Trop Med Hyg. 2011 Apr;84(4):509. doi: 10.4269/ajtmh.2011.10-0687. Am J Trop Med Hyg. 2011. PMID: 21460001 Free PMC article. No abstract available.

2

An unusual febrile nonhemolytic reaction occurred after transfusion in a thalassemia major patient with asymptomatic Plasmodium falciparum infection.

Boschetti C, Cappellini MD, Colombi M, Villa A, Grande R, Vercellati C, Radaelli F, Caspani L, Zanella A. Boschetti C, et al. Transfusion. 2011 Mar;51(3):469-72. doi: 10.1111/j.1537-2995.2010.02853.x. Epub 2010 Aug 23. Transfusion. 2011. PMID: 20735767

3

Clinical and molecular aspects of 23 patients affected by paroxysmal nocturnal hemoglobinuria.

Boschetti C, Fermo E, Bianchi P, Vercellati C, Barraco F, Zanella A. Boschetti C, et al. Am J Hematol. 2004 Sep;77(1):36-44. doi: 10.1002/ajh.20144. Am J Hematol. 2004. PMID: 15307104 Free article. Clinical Trial.

4

Paroxysmal Nocturnal Hemoglobinuria (Pnh): Brain Mri Ischemic Lesions In Neurologically Asymtomatic Patients.

Barcellini W, Scola E, Lanfranconi S, Grottaroli M, Binda F, Fattizzo B, Zaninoni A, Valcamonica G, Cinnante CM, Boschetti C, Buoli M, Altamura CA, Bresolin N, Triulzi F, Zanella A, Cortelezzi A. Barcellini W, et al. Among authors: boschetti c. Sci Rep. 2018 Jan 11;8(1):476. doi: 10.1038/s41598-017-18936-0. Sci Rep. 2018. PMID: 29323198 Free PMC article.

5

Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect.

Mariani M, Barcellini W, Vercellati C, Marcello AP, Fermo E, Pedotti P, Boschetti C, Zanella A. Mariani M, et al. Among authors: boschetti c. Haematologica. 2008 Sep;93(9):1310-7. doi: 10.3324/haematol.12546. Epub 2008 Jul 18. Haematologica. 2008. PMID: 18641031 Free article.

6

Anti-erythroblast autoimmunity in early myelodysplastic syndromes.

Barcellini W, Zaninoni A, Imperiali FG, Boschetti C, Colombi M, Iurlo A, Zanella A. Barcellini W, et al. Among authors: boschetti c. Haematologica. 2007 Jan;92(1):19-26. doi: 10.3324/haematol.10546. Haematologica. 2007. PMID: 17229631 Free article.

7

CDAII presenting as hydrops foetalis: molecular characterization of two cases.

Fermo E, Bianchi P, Notarangelo LD, Binda S, Vercellati C, Marcello AP, Boschetti C, Barcellini W, Zanella A. Fermo E, et al. Among authors: boschetti c. Blood Cells Mol Dis. 2010 Jun 15;45(1):20-2. doi: 10.1016/j.bcmd.2010.03.005. Epub 2010 Apr 9. Blood Cells Mol Dis. 2010. PMID: 20381388

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: boschetti c. Hum Mutat. 2009 Sep;30(9):1292-8. doi: 10.1002/humu.21077. Hum Mutat. 2009. PMID: 19621418

9

Increased resistance of PIG-A- bone marrow progenitors to tumor necrosis factor a and interferon gamma: possible implications for the in vivo dominance of paroxysmal nocturnal hemoglobinuria clones.

Barcellini W, Fermo E, Guia Imperiali F, Zaninoni A, Bianchi P, Boschetti C, Zanella A. Barcellini W, et al. Among authors: boschetti c. Haematologica. 2004 Jun;89(6):651-6. Haematologica. 2004. PMID: 15194531

10

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: boschetti c. 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.

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