Vercellati C - Search Results

1

Case report: Transfusion independence and abolition of extravascular hemolysis in a PNH patient treated with pegcetacoplan.

Fattizzo B, Versino F, Zaninoni A, Marcello APML, Vercellati C, Artuso S, Barcellini W. Fattizzo B, et al. Among authors: vercellati c. Front Immunol. 2022 Dec 1;13:1060923. doi: 10.3389/fimmu.2022.1060923. eCollection 2022. Front Immunol. 2022. PMID: 36532073 Free PMC article.

2

Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase gene.

Fermo E, Bianchi P, Vercellati C, Marcello AP, Garatti M, Marangoni O, Barcellini W, Zanella A. Fermo E, et al. Among authors: vercellati c. Blood Cells Mol Dis. 2008 Jul-Aug;41(1):50-5. doi: 10.1016/j.bcmd.2008.02.002. Epub 2008 Mar 17. Blood Cells Mol Dis. 2008. PMID: 18343696

3

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: vercellati c. Haematologica. 2008 Sep;93(9):1310-7. doi: 10.3324/haematol.12546. Epub 2008 Jul 18. Haematologica. 2008. PMID: 18641031 Free article.

4

A case of congenital red cell pyruvate kinase deficiency associated with hereditary stomatocytosis.

Marcello AP, Vercellati C, Fermo E, Bianchi P, Zaninoni A, Barcellini W, Zanella A. Marcello AP, et al. Among authors: vercellati c. Blood Cells Mol Dis. 2008 Nov-Dec;41(3):261-2. doi: 10.1016/j.bcmd.2008.07.001. Epub 2008 Aug 16. Blood Cells Mol Dis. 2008. PMID: 18708292 No abstract available.

5

Blood p50 evaluation enhances diagnostic definition of isolated erythrocytosis.

Rumi E, Passamonti F, Pagano L, Ammirabile M, Arcaini L, Elena C, Flagiello A, Tedesco R, Vercellati C, Marcello AP, Pietra D, Moratti R, Cazzola M, Lazzarino M. Rumi E, et al. Among authors: vercellati c. J Intern Med. 2009 Feb;265(2):266-74. doi: 10.1111/j.1365-2796.2008.02014.x. Epub 2008 Sep 10. J Intern Med. 2009. PMID: 18793248 Free article.

6

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

7

Triose phosphate isomerase deficiency associated with two novel mutations in TPI gene.

Fermo E, Bianchi P, Vercellati C, Rees DC, Marcello AP, Barcellini W, Zanella A. Fermo E, et al. Among authors: vercellati c. Eur J Haematol. 2010 Aug;85(2):170-3. doi: 10.1111/j.1600-0609.2010.01451.x. Epub 2010 Mar 31. Eur J Haematol. 2010. PMID: 20374271

8

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: vercellati 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

9

Hereditary red cell membrane defects: diagnostic and clinical aspects.

Barcellini W, Bianchi P, Fermo E, Imperiali FG, Marcello AP, Vercellati C, Zaninoni A, Zanella A. Barcellini W, et al. Among authors: vercellati c. Blood Transfus. 2011 Jul;9(3):274-7. doi: 10.2450/2011.0086-10. Epub 2011 Jan 13. Blood Transfus. 2011. PMID: 21251470 Free PMC article. Review. No abstract available.

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: vercellati c. 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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