Zobrazeno 1 - 10
of 13
pro vyhledávání: '"M T Canciani"'
Publikováno v:
Vox sanguinis. 99(3)
Octapharma PPGmbH has recently modified its manufacturing process for solvent/detergent-treated plasma to incorporate a prion reduction step, in which a 3 log reduction has been demonstrated. The current study was undertaken to assess the impact of t
Autor:
J. M. W. Quinn, M. C. Lecomte, S. L. Asplund, K. Sugita, T. J. Huang, T. Matsushita, C. Rahuel, M. Nees, A. Takagi, J. E Compston, H. Okada, M. T. Canciani, S. Bord, M. A. Scott, J. P. Cartron, C. Capoferri, R. E. Lewis, Y. Colin, S. Breit, T. Kojima, W. El Nemer, D. P. Kontoyiannis, A. Yoshioka, J. Takamatsu, E. Frith, E. Gauthier, E. Lee, M. E. Reid, M. Muckenthaler, M. Cole-Sinclair, J. W. Sentry, P. Gane, Y. Kroviarski, A. E. Kulozik, K. Yamamoto, G. Burgess, J. I. O. Craig, M. Pfoersich, M. T. Gillespie, T. Yamazaki, T. Murate, S. H. Kroft, M. Sugimoto, T. Adachi, C. Hagemeier, U. Schaefer, W.-J. Cheng, C. Le Van Kim, F. P. L. Lai, G. R. Halverson, D. C. Ireland, N. J. Karandikar, H.-G. Schneider, P. M. Mannucci, H. Saito, R. W. McKenna
Publikováno v:
British Journal of Haematology. 126
Autor:
L, Baronciani, G, Cozzi, M T, Canciani, F, Peyvandi, A, Srivastava, A B, Federici, P M, Mannucci
Publikováno v:
Thrombosis and haemostasis. 84(4)
Type 3 von Willebrand disease is a rare autosomal disorder characterized by unmeasurable levels of von Willebrand factor and severe hemorrhagic symptoms. We studied a multiethnic group of 37 patients, from Italy (n = 14), Iran (n = 10) and India(n =
Autor:
J, Di Paola, A B, Federici, P M, Mannucci, M T, Canciani, M, Kritzik, T J, Kunicki, D, Nugent
Publikováno v:
Blood. 93(11)
Platelet adhesion to collagen-coated surfaces in whole blood under flow conditions is mediated by both von Willebrand factor (vWF)-dependent recruitment of the platelet glycoprotein Ib-IX receptor complex and collagen interaction with the integrin al
Autor:
C I, Chen, A B, Federici, E M, Cramer, M T, Canciani, P, Harrison, S, Zheng, J M, Massé, P M, Mannucci, C P, Hayward
Publikováno v:
British journal of haematology. 103(1)
In normal platelet alpha-granules von Willebrand factor (VWF) is stored with multimerin and factor V in an eccentric electron-lucent zone. Because the platelet stores of VWF are deficient in 'platelet low' type 1 and type 3 von Willebrand disease (VW
Publikováno v:
Blood. 92(8)
Patients with monoclonal gammopathies of uncertain significance (MGUS) may develop an acquired bleeding disorder similar to congenital von Willebrand disease, called acquired von Willebrand syndrome (AvWS). In these patients, measures to improve hemo
Autor:
A B, Federici, P M, Mannucci, F, Stabile, M T, Canciani, N, Di Rocco, S, Miyata, J, Ware, Z M, Ruggeri
Type 2B von Willebrand disease (vWD) is typically characterized by enhanced ristocetin-induced platelet aggregation (RIPA) caused by increased von Willebrand factor (vWF) affinity for platelets. Furthermore, absence of larger vWF multimers in plasma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::98fade41cf5fd18b6ebb76d0d3bdf4e6
http://hdl.handle.net/2434/215725
http://hdl.handle.net/2434/215725
Publikováno v:
Thrombosis and haemostasis. 60(2)
We have studied the interaction of ASvWf with human platelets in PRP and in suspensions of washed platelets containing either physiological or low external ionized calcium concentration [Ca2+]o. In hirudin-PRP or in washed platelets in 1.5-2 mM CaCl2
Publikováno v:
XIth International Congress on Thrombosis and Haemostasis.
Human platelets aggregated by thrombin (T) under conditions in which the release reaction (RR) occurs to only a small extent can be deaggregated by agents that dissociate 125I-fibrinogen bound to platelets. In contrast, when platelets undergo the RR,
Publikováno v:
Haematologica. 64(3)