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Barbara Lunghi

Showing results (1-10 of 40) with videos related to

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Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|April 6, 2007
Factor V Kuwait alias factor V R3: a rare polymorphism of uncertain functional significanceElisabetta Castoldi, Barbara Lunghi, Jan Rosing, et al.
Thrombosis Research|November 22, 2011
Functional geneticsGiovanna Marchetti, Mirko Pinotti, Barbara Lunghi, et al.
Haematologica|March 4, 2008
Evaluation of factor V mRNA to define the residual factor V expression levels in severe factor V deficiencyBarbara Lunghi, Mirko Pinotti, Iva Maestri, et al.
Thrombosis Research|May 29, 2012
The F11 rs2289252 polymorphism is associated with FXI activity levels and APTT ratio in women with thrombosisBarbara Lunghi, Michela Cini, Cristina Legnani, et al.
Thrombosis and Haemostasis|March 1, 2005
The factor VIII D1241E polymorphism is associated with decreased factor VIII activity and not with activated protein C resistance levelsDaniela Scanavini, Cristina Legnani, Barbara Lunghi, et al.
Thrombosis and Haemostasis|April 9, 2008
Influence of low-density lipoprotein (LDL) receptor-related protein and ABO blood group genotypes on factor XI levelsGiovanna Marchetti, Barbara Lunghi, Gianni Mazzoni, et al.
Blood|June 18, 2005
An underestimated combination of opposites resulting in enhanced thrombotic tendencyPaolo Simioni, Elisabetta Castoldi, Barbara Lunghi, et al.
Journal of Clinical Medicine|February 15, 2022
Combination of <i>CLEC4M</i> rs868875 G-Carriership and <i>ABO</i> O Genotypes May Predict Faster Decay of FVIII Infused in Hemophilia A PatientsBarbara Lunghi, Massimo Morfini, Nicola Martinelli, et al.
Haematologica|February 12, 2002
Reduced inhibition of activated prothrombin by heparin and venous thromboembolism: heparin resistance revisitedCristina Legnani, Luigi Preda, Gualtiero Palareti, et al.
Thrombosis and Haemostasis|April 26, 2013
Molecular basis of coagulation factor V deficiency caused by the R1698W inter-domain mutationSara Calzavarini, Bruno O Villoutreix, Barbara Lunghi, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|April 6, 2007
Factor V Kuwait alias factor V R3: a rare polymorphism of uncertain functional significanceElisabetta Castoldi, Barbara Lunghi, Jan Rosing, et al.
Thrombosis Research|November 22, 2011
Functional geneticsGiovanna Marchetti, Mirko Pinotti, Barbara Lunghi, et al.
Haematologica|March 4, 2008
Evaluation of factor V mRNA to define the residual factor V expression levels in severe factor V deficiencyBarbara Lunghi, Mirko Pinotti, Iva Maestri, et al.
Thrombosis Research|May 29, 2012
The F11 rs2289252 polymorphism is associated with FXI activity levels and APTT ratio in women with thrombosisBarbara Lunghi, Michela Cini, Cristina Legnani, et al.
Thrombosis and Haemostasis|March 1, 2005
The factor VIII D1241E polymorphism is associated with decreased factor VIII activity and not with activated protein C resistance levelsDaniela Scanavini, Cristina Legnani, Barbara Lunghi, et al.
Thrombosis and Haemostasis|April 9, 2008
Influence of low-density lipoprotein (LDL) receptor-related protein and ABO blood group genotypes on factor XI levelsGiovanna Marchetti, Barbara Lunghi, Gianni Mazzoni, et al.
Blood|June 18, 2005
An underestimated combination of opposites resulting in enhanced thrombotic tendencyPaolo Simioni, Elisabetta Castoldi, Barbara Lunghi, et al.
Journal of Clinical Medicine|February 15, 2022
Combination of <i>CLEC4M</i> rs868875 G-Carriership and <i>ABO</i> O Genotypes May Predict Faster Decay of FVIII Infused in Hemophilia A PatientsBarbara Lunghi, Massimo Morfini, Nicola Martinelli, et al.
Haematologica|February 12, 2002
Reduced inhibition of activated prothrombin by heparin and venous thromboembolism: heparin resistance revisitedCristina Legnani, Luigi Preda, Gualtiero Palareti, et al.
Thrombosis and Haemostasis|April 26, 2013
Molecular basis of coagulation factor V deficiency caused by the R1698W inter-domain mutationSara Calzavarini, Bruno O Villoutreix, Barbara Lunghi, et al.
Pageof 4