Federici AB - Search Results

1

A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3.

Schneppenheim R, Castaman G, Federici AB, Kreuz W, Marschalek R, Oldenburg J, Oyen F, Budde U. Schneppenheim R, et al. Among authors: federici ab. J Thromb Haemost. 2007 Apr;5(4):722-8. doi: 10.1111/j.1538-7836.2007.02460.x. Epub 2007 Feb 26. J Thromb Haemost. 2007. PMID: 17371490 Free article.

2

In vivo experiments indicate that relatively high platelet deposition in von Willebrand's disease 'Vicenza' is caused by normal platelet-VWF levels rather than by high VWF-multimers in plasma.

d'Alessio PA, Castaman G, Rodeghiero F, de Boer HC, Federici AB, Mannucci PM, de Groot PG, Sixma JJ, Zwaginga JJ. d'Alessio PA, et al. Among authors: federici ab. Thromb Res. 1992 Jan 15;65(2):221-8. doi: 10.1016/0049-3848(92)90242-3. Thromb Res. 1992. PMID: 1579897

3

Platelet adhesion to collagen in subtypes of type I von Willebrand's disease is dependent on platelet von Willebrand factor.

d'Alessio P, Zwaginga JJ, de Boer HC, Federici AB, Rodeghiero F, Castaman G, Mariani G, Mannucci PM, de Groot PG, Sixma JJ. d'Alessio P, et al. Among authors: federici ab. Thromb Haemost. 1990 Oct 22;64(2):227-31. Thromb Haemost. 1990. PMID: 2125373

4

Type IIB von Willebrand factor with normal sialic acid content induces platelet aggregation in the absence of ristocetin. Role of platelet activation, fibrinogen, and two distinct membrane receptors.

De Marco L, Mazzuccato M, Grazia Del Ben M, Budde U, Federici AB, Girolami A, Ruggeri ZM. De Marco L, et al. Among authors: federici ab. J Clin Invest. 1987 Aug;80(2):475-82. doi: 10.1172/JCI113095. J Clin Invest. 1987. PMID: 3038958 Free PMC article.

5

Ex vivo experimental thrombosis in variants of von Willebrand disease.

Fressinaud E, Federici AB, Castaman G, Mannucci PM, Meyer D. Fressinaud E, et al. Among authors: federici ab. C R Acad Sci III. 1993 Oct;316(10):1260-5. C R Acad Sci III. 1993. PMID: 8062135

6

Autopsy findings in three patients with von Willebrand disease type IIB and type III: presence of atherosclerotic lesions without occlusive arterial thrombi.

Federici AB, Mannucci PM, Fogato E, Ghidoni P, Matturri L. Federici AB, et al. Thromb Haemost. 1993 Nov 15;70(5):758-61. Thromb Haemost. 1993. PMID: 8128431

7

The role of platelet von Willebrand factor in platelet adhesion and thrombus formation: a study of 34 patients with various subtypes of type I von Willebrand disease.

Fressinaud E, Federici AB, Castaman G, Rothschild C, Rodeghiero F, Baumgartner HR, Mannucci PM, Meyer D. Fressinaud E, et al. Among authors: federici ab. Br J Haematol. 1994 Feb;86(2):327-32. doi: 10.1111/j.1365-2141.1994.tb04734.x. Br J Haematol. 1994. PMID: 8199022

8

A type 2b von Willebrand disease mutation (Ile546-->Val) associated with an unusual phenotype.

Federici AB, Mannucci PM, Stabile F, Canciani MT, Di Rocco N, Miyata S, Ware J, Ruggeri ZM. Federici AB, et al. Thromb Haemost. 1997 Sep;78(3):1132-7. Thromb Haemost. 1997. PMID: 9308766

9

Treatment of acquired von Willebrand syndrome in patients with monoclonal gammopathy of uncertain significance: comparison of three different therapeutic approaches.

Federici AB, Stabile F, Castaman G, Canciani MT, Mannucci PM. Federici AB, et al. Blood. 1998 Oct 15;92(8):2707-11. Blood. 1998. PMID: 9763553 Free article. Clinical Trial.

10

Evaluation of the PFA-100 system in the diagnosis and therapeutic monitoring of patients with von Willebrand disease.

Cattaneo M, Federici AB, Lecchi A, Agati B, Lombardi R, Stabile F, Bucciarelli P. Cattaneo M, et al. Among authors: federici ab. Thromb Haemost. 1999 Jul;82(1):35-9. Thromb Haemost. 1999. PMID: 10456451

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