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M T Canciani

Showing results (11-20 of 24) with videos related to

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Thrombosis and Haemostasis|October 31, 1988
Conditions influencing the interaction of asialo von Willebrand factor with human platelets--the effects of external ionized calcium concentration and the role of arachidonate pathwayM Cattaneo, J F Mustard, M T Canciani, et al.
Thrombosis and Haemostasis|November 1, 2000
Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand diseaseL Baronciani, G Cozzi, M T Canciani, et al.
Vox Sanguinis|September 16, 2010
The effect of prion reduction in solvent/detergent-treated plasma on haemostatic variablesA S Lawrie, L Green, M T Canciani, et al.
Blood|May 26, 1999
Low platelet alpha2beta1 levels in type I von Willebrand disease correlate with impaired platelet function in a high shear stress systemJ Di Paola, A B Federici, P M Mannucci, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 11, 2008
Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand diseaseL Baronciani, A B Federici, G Cozzi, et al.
Blood|March 1, 1990
Released adenosine diphosphate stabilizes thrombin-induced human platelet aggregatesM Cattaneo, M T Canciani, A Lecchi, et al.
Thrombosis and Haemostasis|October 6, 1997
A type 2b von Willebrand disease mutation (Ile546-->Val) associated with an unusual phenotypeA B Federici, P M Mannucci, F Stabile, et al.
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigreesT J Kunicki, L Baronciani, M T Canciani, et al.
Journal of Thrombosis and Haemostasis : JTH|April 30, 2013
A synonymous (c.3390C>T) or a splice-site (c.3380-2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE)M T Pagliari, L Baronciani, I Garcìa Oya, et al.
Journal of Thrombosis and Haemostasis : JTH|May 9, 2009
Type 2A (IIH) von Willebrand disease is due to mutations that affect von Willebrand factor multimerizationL Baronciani, A B Federici, M Punzo, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Thrombosis and Haemostasis|October 31, 1988
Conditions influencing the interaction of asialo von Willebrand factor with human platelets--the effects of external ionized calcium concentration and the role of arachidonate pathwayM Cattaneo, J F Mustard, M T Canciani, et al.
Thrombosis and Haemostasis|November 1, 2000
Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand diseaseL Baronciani, G Cozzi, M T Canciani, et al.
Vox Sanguinis|September 16, 2010
The effect of prion reduction in solvent/detergent-treated plasma on haemostatic variablesA S Lawrie, L Green, M T Canciani, et al.
Blood|May 26, 1999
Low platelet alpha2beta1 levels in type I von Willebrand disease correlate with impaired platelet function in a high shear stress systemJ Di Paola, A B Federici, P M Mannucci, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 11, 2008
Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand diseaseL Baronciani, A B Federici, G Cozzi, et al.
Blood|March 1, 1990
Released adenosine diphosphate stabilizes thrombin-induced human platelet aggregatesM Cattaneo, M T Canciani, A Lecchi, et al.
Thrombosis and Haemostasis|October 6, 1997
A type 2b von Willebrand disease mutation (Ile546-->Val) associated with an unusual phenotypeA B Federici, P M Mannucci, F Stabile, et al.
Journal of Thrombosis and Haemostasis : JTH|January 18, 2006
An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigreesT J Kunicki, L Baronciani, M T Canciani, et al.
Journal of Thrombosis and Haemostasis : JTH|April 30, 2013
A synonymous (c.3390C>T) or a splice-site (c.3380-2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE)M T Pagliari, L Baronciani, I Garcìa Oya, et al.
Journal of Thrombosis and Haemostasis : JTH|May 9, 2009
Type 2A (IIH) von Willebrand disease is due to mutations that affect von Willebrand factor multimerizationL Baronciani, A B Federici, M Punzo, et al.
Pageof 3