Vercellati C - Search Results

1

Detection of red blood cell antibodies in mitogen-stimulated cultures from patients with hereditary spherocytosis.

Zaninoni A, Vercellati C, Imperiali FG, Marcello AP, Fattizzo B, Fermo E, Bianchi P, Grossi C, Cattaneo A, Cortelezzi A, Zanella A, Barcellini W. Zaninoni A, et al. Among authors: vercellati c. Transfusion. 2015 Dec;55(12):2930-8. doi: 10.1111/trf.13257. Epub 2015 Aug 10. Transfusion. 2015. PMID: 26259504

2

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

Zanella A, Bianchi P, Baronciani L, Zappa M, Bredi E, Vercellati C, Alfinito F, Pelissero G, Sirchia G. Zanella A, et al. Among authors: vercellati c. Blood. 1997 May 15;89(10):3847-52. Blood. 1997. PMID: 9160692 Free article.

3

A variant of the EPB3 gene of the anti-Lepore type in hereditary spherocytosis.

Bianchi P, Zanella A, Alloisio N, Barosi G, Bredi E, Pelissero G, Zappa M, Vercellati C, Baronciani L, Delaunay J, Sirchia G. Bianchi P, et al. Among authors: vercellati c. Br J Haematol. 1997 Aug;98(2):283-8. doi: 10.1046/j.1365-2141.1997.1983013.x. Br J Haematol. 1997. PMID: 9266920 Free article.

4

A case of complete adenylate kinase deficiency due to a nonsense mutation in AK-1 gene (Arg 107 --> Stop, CGA --> TGA) associated with chronic haemolytic anaemia.

Bianchi P, Zappa M, Bredi E, Vercellati C, Pelissero G, Barraco F, Zanella A. Bianchi P, et al. Among authors: vercellati c. Br J Haematol. 1999 Apr;105(1):75-9. Br J Haematol. 1999. PMID: 10233365 Free article.

5

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: vercellati 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.

6

Cell age-related monovalent cations content and density changes in stored human erythrocytes.

Minetti G, Ciana A, Profumo A, Zappa M, Vercellati C, Zanella A, Arduini A, Brovelli A. Minetti G, et al. Among authors: vercellati c. Biochim Biophys Acta. 2001 Aug 15;1527(3):149-55. doi: 10.1016/s0304-4165(01)00159-3. Biochim Biophys Acta. 2001. PMID: 11479031

7

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

8

Molecular characterization of six unrelated Italian patients affected by pyrimidine 5'-nucleotidase deficiency.

Bianchi P, Fermo E, Alfinito F, Vercellati C, Baserga M, Ferraro F, Guzzo I, Rotoli B, Zanella A. Bianchi P, et al. Among authors: vercellati c. Br J Haematol. 2003 Sep;122(5):847-51. doi: 10.1046/j.1365-2141.2003.04532.x. Br J Haematol. 2003. PMID: 12930399 Free article.

9

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. Among authors: vercellati c. Am J Hematol. 2004 Sep;77(1):36-44. doi: 10.1002/ajh.20144. Am J Hematol. 2004. PMID: 15307104 Free article. Clinical Trial.

10

A new variant of adenylate kinase (delG138) associated with severe hemolytic anemia.

Fermo E, Bianchi P, Vercellati C, Micheli S, Marcello AP, Portaleone D, Zanella A. Fermo E, et al. Among authors: vercellati c. Blood Cells Mol Dis. 2004 Sep-Oct;33(2):146-9. doi: 10.1016/j.bcmd.2004.06.002. Blood Cells Mol Dis. 2004. PMID: 15315793

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