Federici AB - Search Results

1

Management of inherited von Willebrand disease in Italy: results from the retrospective study on 1234 patients.

Federici AB, Bucciarelli P, Castaman G, Baronciani L, Canciani MT, Mazzucconi MG, Morfini M, Rocino A, Schiavoni M, Oliovecchio E, Iorio A, Mannucci PM. Federici AB, et al. Semin Thromb Hemost. 2011 Jul;37(5):511-21. doi: 10.1055/s-0031-1281037. Epub 2011 Nov 18. Semin Thromb Hemost. 2011. PMID: 22102194 Free article.

2

Advances in the genetics and treatment of von Willebrand disease.

Federici AB, Mannucci PM. Federici AB, et al. Curr Opin Pediatr. 2002 Feb;14(1):23-33. doi: 10.1097/00008480-200202000-00005. Curr Opin Pediatr. 2002. PMID: 11880730 Review.

3

Von Willebrand's disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatment.

Castaman G, Federici AB, Rodeghiero F, Mannucci PM. Castaman G, et al. Among authors: federici ab. Haematologica. 2003 Jan;88(1):94-108. Haematologica. 2003. PMID: 12551832 Free article. Review.

4

Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients.

Baronciani L, Cozzi G, Canciani MT, Peyvandi F, Srivastava A, Federici AB, Mannucci PM. Baronciani L, et al. Among authors: federici ab. Blood Cells Mol Dis. 2003 May-Jun;30(3):264-70. doi: 10.1016/s1079-9796(03)00033-0. Blood Cells Mol Dis. 2003. PMID: 12737944

5

The factor VIII/von Willebrand factor complex: basic and clinical issues.

Federici AB. Federici AB. Haematologica. 2003 Jun;88(6):EREP02. Haematologica. 2003. PMID: 12826528 Review.

6

Mild forms of von Willebrand disease: diagnosis and management.

Federici AB. Federici AB. Curr Hematol Rep. 2003 Sep;2(5):373-80. Curr Hematol Rep. 2003. PMID: 12932308

7

Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study.

Federici AB, Mazurier C, Berntorp E, Lee CA, Scharrer I, Goudemand J, Lethagen S, Nitu I, Ludwig G, Hilbert L, Mannucci PM. Federici AB, et al. Blood. 2004 Mar 15;103(6):2032-8. doi: 10.1182/blood-2003-06-2072. Epub 2003 Nov 20. Blood. 2004. PMID: 14630825 Free article. Clinical Trial.

8

A sensitive ristocetin co-factor activity assay with recombinant glycoprotein Ibalpha for the diagnosis of patients with low von Willebrand factor levels.

Federici AB, Canciani MT, Forza I, Mannucci PM, Marchese P, Ware J, Ruggeri ZM. Federici AB, et al. Haematologica. 2004 Jan;89(1):77-85. Haematologica. 2004. PMID: 14754609 Free article.

9

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees.

Kunicki TJ, Federici AB, Salomon DR, Koziol JA, Head SR, Mondala TS, Chismar JD, Baronciani L, Canciani MT, Peake IR. Kunicki TJ, et al. Among authors: federici ab. Blood. 2004 Oct 15;104(8):2359-67. doi: 10.1182/blood-2004-01-0349. Epub 2004 Jun 29. Blood. 2004. PMID: 15226188 Free article.

10

A new candidate mutation, G1629R, in a patient with type 2A von Willebrand's disease: basic mechanisms and clinical implications.

Hilbert L, Federici AB, Baronciani L, Dallagiovanna S, Mazurier C. Hilbert L, et al. Among authors: federici ab. Haematologica. 2004 Sep;89(9):1128-33. Haematologica. 2004. PMID: 15377475 Free article.

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