Bianchi P - Search Results

1

The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper.

Roy NBA, Da Costa L, Russo R, Bianchi P, Mañú-Pereira MDM, Fermo E, Andolfo I, Clark B, Proven M, Sanchez M, van Wijk R, van der Zwaag B, Layton M, Rees D, Iolascon A; British Society for Haematology/ European Hematology Association. Roy NBA, et al. Among authors: bianchi p. Br J Haematol. 2022 Aug;198(3):459-477. doi: 10.1111/bjh.18191. Epub 2022 Jun 6. Br J Haematol. 2022. PMID: 35661144 No abstract available.

2

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. 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.

3

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: bianchi p. Haematologica. 2004 Jun;89(6):651-6. Haematologica. 2004. PMID: 15194531

4

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

5

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: bianchi p. 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

6

Functional analysis of pyrimidine 5'-nucleotidase mutants causing nonspherocytic hemolytic anemia.

Chiarelli LR, Bianchi P, Fermo E, Galizzi A, Iadarola P, Mattevi A, Zanella A, Valentini G. Chiarelli LR, et al. Among authors: bianchi p. Blood. 2005 Apr 15;105(8):3340-5. doi: 10.1182/blood-2004-10-3895. Epub 2004 Dec 16. Blood. 2005. PMID: 15604219 Free article.

7

Red cell pyruvate kinase deficiency: 17 new mutations of the PK-LR gene.

Fermo E, Bianchi P, Chiarelli LR, Cotton F, Vercellati C, Writzl K, Baker K, Hann I, Rodwell R, Valentini G, Zanella A. Fermo E, et al. Among authors: bianchi p. Br J Haematol. 2005 Jun;129(6):839-46. doi: 10.1111/j.1365-2141.2005.05520.x. Br J Haematol. 2005. PMID: 15953013 Free article.

8

Red cell pyruvate kinase deficiency: molecular and clinical aspects.

Zanella A, Fermo E, Bianchi P, Valentini G. Zanella A, et al. Among authors: bianchi p. Br J Haematol. 2005 Jul;130(1):11-25. doi: 10.1111/j.1365-2141.2005.05527.x. Br J Haematol. 2005. PMID: 15982340 Free article. Review.

9

Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestations.

Zanella A, Bianchi P, Fermo E, Valentini G. Zanella A, et al. Among authors: bianchi p. Br J Haematol. 2006 Apr;133(2):113-23. doi: 10.1111/j.1365-2141.2006.05992.x. Br J Haematol. 2006. PMID: 16611302 Free article. Review.

10

Two new mutations of the P5'N-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorder.

Chiarelli LR, Fermo E, Abrusci P, Bianchi P, Dellacasa CM, Galizzi A, Zanella A, Valentini G. Chiarelli LR, et al. Among authors: bianchi p. Haematologica. 2006 Sep;91(9):1244-7. Haematologica. 2006. PMID: 16956825

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