Bianchi P - Search Results

1

Study of the molecular defects in glucose phosphate isomerase-deficient patients affected by chronic hemolytic anemia.

Baronciani L, Zanella A, Bianchi P, Zappa M, Alfinito F, Iolascon A, Tannoia N, Beutler E, Sirchia G. Baronciani L, et al. Among authors: bianchi p. Blood. 1996 Sep 15;88(6):2306-10. Blood. 1996. PMID: 8822952 Free article.

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: bianchi p. Blood. 1997 May 15;89(10):3847-52. Blood. 1997. PMID: 9160692 Free article.

3

Hematologically important mutations: red cell pyruvate kinase (2nd update).

Baronciani L, Bianchi P, Zanella A. Baronciani L, et al. Among authors: bianchi p. Blood Cells Mol Dis. 1998 Sep;24(3):273-9. doi: 10.1006/bcmd.1998.0193. Blood Cells Mol Dis. 1998. PMID: 10087985 Review. No abstract available.

4

Hematologically important mutations: red cell pyruvate kinase (Third update).

Bianchi P, Zanella A. Bianchi P, et al. Blood Cells Mol Dis. 2000 Feb;26(1):47-53. doi: 10.1006/bcmd.2000.0276. Blood Cells Mol Dis. 2000. PMID: 10772876 No abstract available.

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: bianchi p. 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

Hematologically important mutations: red cell pyruvate kinase.

Baronciani L, Bianchi P, Zanella A. Baronciani L, et al. Among authors: bianchi p. Blood Cells Mol Dis. 1996;22(1):85-9. doi: 10.1006/bcmd.1996.0012. Blood Cells Mol Dis. 1996. PMID: 8807089 No abstract available.

7

Human erythrocyte pyruvate kinase: characterization of the recombinant enzyme and a mutant form (R510Q) causing nonspherocytic hemolytic anemia.

Wang C, Chiarelli LR, Bianchi P, Abraham DJ, Galizzi A, Mattevi A, Zanella A, Valentini G. Wang C, et al. Among authors: bianchi p. Blood. 2001 Nov 15;98(10):3113-20. doi: 10.1182/blood.v98.10.3113. Blood. 2001. PMID: 11698298 Free article.

8

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

9

Hematologically important mutations: red cell pyruvate kinase (1st update).

Baronciani L, Bianchi P, Zanella A. Baronciani L, et al. Among authors: bianchi p. Blood Cells Mol Dis. 1996;22(3):259-64. doi: 10.1006/bcmd.1996.0107. Blood Cells Mol Dis. 1996. PMID: 9075576 No abstract available.

10

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. 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.

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