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C M Millar

Showing results (1-10 of 11) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|November 13, 2013
Measurement of factor IX activity in plasma-derived and recombinant concentrates: insights from thrombin generation and activation-based assaysY Yu, C M Millar
BJA Education|January 18, 2021
Haemostatic disorders in pregnancyR Agarwala, C M Millar, J P Campbell
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 31, 2008
Consideration of platelet function disorders in patients with reduced VWF levelsC M Millar, A F Riddell, E G Tuddenham
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 15, 2011
Pregnancy in type 2B VWD: a case seriesA Ranger, R A Manning, H Lyall, et al.
British Journal of Haematology|July 27, 2005
The Y/C1584 mutation of von Willebrand factor in type 2M von Willebrand disease: frequency and clearance of von Willebrand factorC M Millar, A F Riddel, A Griffioe, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 25, 2016
Experience of a new high-purity factor X concentrate in subjects with hereditary factor X deficiency undergoing surgeryM A Escobar, G Auerswald, S Austin, et al.
Journal of Thrombosis and Haemostasis : JTH|April 28, 2012
Characterisation of von Willebrand factor A1 domain mutants I1416N and I1416T: correlation of clinical phenotype with flow-based platelet adhesionT A J McKinnon, A A Nowak, J Cutler, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 22, 2010
Risk reduction strategies for variant Creutzfeldt-Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disordersC M Millar, N Connor, G Dolan, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 15, 2010
Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophiliaA Peden, L McCardle, M W Head, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 24, 2011
The risk of variant Creutzfeldt-Jakob disease among UK patients with bleeding disorders, known to have received potentially contaminated plasma productsS M A Zaman, F G H Hill, B Palmer, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Thrombosis and Haemostasis : JTH|November 13, 2013
Measurement of factor IX activity in plasma-derived and recombinant concentrates: insights from thrombin generation and activation-based assaysY Yu, C M Millar
BJA Education|January 18, 2021
Haemostatic disorders in pregnancyR Agarwala, C M Millar, J P Campbell
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 31, 2008
Consideration of platelet function disorders in patients with reduced VWF levelsC M Millar, A F Riddell, E G Tuddenham
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 15, 2011
Pregnancy in type 2B VWD: a case seriesA Ranger, R A Manning, H Lyall, et al.
British Journal of Haematology|July 27, 2005
The Y/C1584 mutation of von Willebrand factor in type 2M von Willebrand disease: frequency and clearance of von Willebrand factorC M Millar, A F Riddel, A Griffioe, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 25, 2016
Experience of a new high-purity factor X concentrate in subjects with hereditary factor X deficiency undergoing surgeryM A Escobar, G Auerswald, S Austin, et al.
Journal of Thrombosis and Haemostasis : JTH|April 28, 2012
Characterisation of von Willebrand factor A1 domain mutants I1416N and I1416T: correlation of clinical phenotype with flow-based platelet adhesionT A J McKinnon, A A Nowak, J Cutler, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 22, 2010
Risk reduction strategies for variant Creutzfeldt-Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disordersC M Millar, N Connor, G Dolan, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 15, 2010
Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophiliaA Peden, L McCardle, M W Head, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 24, 2011
The risk of variant Creutzfeldt-Jakob disease among UK patients with bleeding disorders, known to have received potentially contaminated plasma productsS M A Zaman, F G H Hill, B Palmer, et al.
Pageof 2