Mannucci PM - Search Results

1

A new variant of von Willebrand disease (type II I) with a normal degree of proteolytic cleavage of von Willebrand factor.

Castaman G, Rodeghiero F, Lattuada A, Mannucci PM. Castaman G, et al. Among authors: mannucci pm. Thromb Res. 1992 Feb 1;65(3):343-51. doi: 10.1016/0049-3848(92)90165-7. Thromb Res. 1992. PMID: 1631800

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: mannucci pm. Thromb Res. 1992 Jan 15;65(2):221-8. doi: 10.1016/0049-3848(92)90242-3. Thromb Res. 1992. PMID: 1579897

3

Comparison of four virus-inactivated plasma concentrates for treatment of severe von Willebrand disease: a cross-over randomized trial.

Mannucci PM, Tenconi PM, Castaman G, Rodeghiero F. Mannucci PM, et al. Blood. 1992 Jun 15;79(12):3130-7. Blood. 1992. PMID: 1596562 Free article. Clinical Trial.

4

Subunit composition of plasma von Willebrand factor (vWF) in two uremic patients with acquired vWF abnormalities.

Castaman G, Rodeghiero F, Lattuada A, Mannucci PM. Castaman G, et al. Among authors: mannucci pm. Thromb Haemost. 1992 Jan 23;67(1):183. Thromb Haemost. 1992. PMID: 1615475 No abstract available.

5

Replacement therapy with virus-inactivated plasma concentrates in von Willebrand disease.

Rodeghiero F, Castaman G, Meyer D, Mannucci PM. Rodeghiero F, et al. Among authors: mannucci pm. Vox Sang. 1992;62(4):193-9. doi: 10.1111/j.1423-0410.1992.tb01198.x. Vox Sang. 1992. PMID: 1642002 Review.

6

Clinical indications for desmopressin (DDAVP) in congenital and acquired von Willebrand disease.

Rodeghiero F, Castaman G, Mannucci PM. Rodeghiero F, et al. Among authors: mannucci pm. Blood Rev. 1991 Sep;5(3):155-61. doi: 10.1016/0268-960x(91)90032-8. Blood Rev. 1991. PMID: 1777748 Review.

7

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: mannucci pm. Thromb Haemost. 1990 Oct 22;64(2):227-31. Thromb Haemost. 1990. PMID: 2125373

8

Platelet von Willebrand factor assay: results using two methods for platelet lysis.

Rodeghiero F, Castaman GC, Tosetto A, Lattuada A, Mannucci PM. Rodeghiero F, et al. Among authors: mannucci pm. Thromb Res. 1990 Jul 15;59(2):259-67. doi: 10.1016/0049-3848(90)90129-z. Thromb Res. 1990. PMID: 2237811

9

Heterogeneous phenotypes of platelet and plasma von Willebrand factor in obligatory heterozygotes for severe von Willebrand disease.

Mannucci PM, Lattuada A, Castaman G, Lombardi R, Colibretti ML, Ciavarella N, Rodeghiero F. Mannucci PM, et al. Blood. 1989 Nov 15;74(7):2433-6. Blood. 1989. PMID: 2804373 Free article.

10

Hyper-responsiveness to DDAVP for patients with type I von Willebrand's disease and normal intra-platelet von Willebrand factor.

Rodeghiero F, Castaman G, Di Bona E, Ruggeri M, Lombardi R, Mannucci PM. Rodeghiero F, et al. Among authors: mannucci pm. Eur J Haematol. 1988 Feb;40(2):163-7. doi: 10.1111/j.1600-0609.1988.tb00815.x. Eur J Haematol. 1988. PMID: 3126081

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