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Ezio Zanon

Showing results (31-40 of 77) with videos related to

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 30, 2003
A novel type I factor X variant (factor X Cys350Phe) due to loss of a disulfide bond in the catalytic domainFabrizio Vianello, Anna Maria Lombardi, Federico Dal Bello, et al.
Seminars in Thrombosis and Hemostasis|September 12, 2013
Systematic review of the role of FVIII concentrates in inhibitor development in previously untreated patients with severe hemophilia a: a 2013 updateMassimo Franchini, Antonio Coppola, Angiola Rocino, et al.
Thrombosis Research|November 5, 2002
Conformation sensitive gel electrophoresis for detection of factor X gene mutationsFabrizio Vianello, Anna Maria Lombardi, Federico Dal Bello, et al.
Thrombosis and Haemostasis|December 4, 2003
Severe prekallikrein (Fletcher factor) deficiency due to a compound heterozygosis (383Trp stop codon and Cys529Tyr)Anna Maria Lombardi, Maria Teresa Sartori, Laura Cabrio, et al.
International Journal of General Medicine|April 27, 2012
Autonomic dysfunction and primary antiphospholipid syndrome: a frequent and frightening correlation?Franca Bilora, Michela Biasiolo, Alice Zancan, et al.
Thrombosis and Haemostasis|September 1, 2010
Management of dental extraction in patients undergoing anticoagulant treatment. Results from a large, multicentre, prospective, case-control studyChristian Bacci, Michele Maglione, Lorenzo Favero, et al.
Thrombosis Research|October 28, 2015
Activated prothrombin complex concentrate (FEIBA®) for the treatment and prevention of bleeding in patients with acquired haemophilia: A sequential studyEzio Zanon, Marta Milan, Gabriella Gamba, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 26, 2004
A large deletion due to a new mutation (intron 13/exon 23) in a sporadic case of severe hemophilia AAnna Maria Lombardi, Laura Cabrio, Ezio Zanon, et al.
Thrombosis Research|September 2, 2014
Cognitive dysfunctions and cerebral microbleeds in adult patients with haemophilia A: a clinical and MRI pilot-studyEzio Zanon, Renzo Manara, Marta Milan, et al.
International Journal of General Medicine|August 7, 2010
Patient preference for needleless factor VIII reconstitution device: the Italian experienceRoberto Musso, Rita Santoro, Antonio Coppola, et al.
Pageof 8

Showing results (31-40 of 77) with videos related to

Sort By:
Pageof 8
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 30, 2003
A novel type I factor X variant (factor X Cys350Phe) due to loss of a disulfide bond in the catalytic domainFabrizio Vianello, Anna Maria Lombardi, Federico Dal Bello, et al.
Seminars in Thrombosis and Hemostasis|September 12, 2013
Systematic review of the role of FVIII concentrates in inhibitor development in previously untreated patients with severe hemophilia a: a 2013 updateMassimo Franchini, Antonio Coppola, Angiola Rocino, et al.
Thrombosis Research|November 5, 2002
Conformation sensitive gel electrophoresis for detection of factor X gene mutationsFabrizio Vianello, Anna Maria Lombardi, Federico Dal Bello, et al.
Thrombosis and Haemostasis|December 4, 2003
Severe prekallikrein (Fletcher factor) deficiency due to a compound heterozygosis (383Trp stop codon and Cys529Tyr)Anna Maria Lombardi, Maria Teresa Sartori, Laura Cabrio, et al.
International Journal of General Medicine|April 27, 2012
Autonomic dysfunction and primary antiphospholipid syndrome: a frequent and frightening correlation?Franca Bilora, Michela Biasiolo, Alice Zancan, et al.
Thrombosis and Haemostasis|September 1, 2010
Management of dental extraction in patients undergoing anticoagulant treatment. Results from a large, multicentre, prospective, case-control studyChristian Bacci, Michele Maglione, Lorenzo Favero, et al.
Thrombosis Research|October 28, 2015
Activated prothrombin complex concentrate (FEIBA®) for the treatment and prevention of bleeding in patients with acquired haemophilia: A sequential studyEzio Zanon, Marta Milan, Gabriella Gamba, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 26, 2004
A large deletion due to a new mutation (intron 13/exon 23) in a sporadic case of severe hemophilia AAnna Maria Lombardi, Laura Cabrio, Ezio Zanon, et al.
Thrombosis Research|September 2, 2014
Cognitive dysfunctions and cerebral microbleeds in adult patients with haemophilia A: a clinical and MRI pilot-studyEzio Zanon, Renzo Manara, Marta Milan, et al.
International Journal of General Medicine|August 7, 2010
Patient preference for needleless factor VIII reconstitution device: the Italian experienceRoberto Musso, Rita Santoro, Antonio Coppola, et al.
Pageof 8