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R I Baker

Showing results (31-40 of 41) with videos related to

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European Journal of Clinical Nutrition|October 11, 2001
Effects of regular ingestion of black tea on haemostasis and cell adhesion molecules in humansJ M Hodgson, I B Puddey, T A Mori, et al.
Journal of the American College of Cardiology|June 25, 2003
A rapid protocol for the prevention of contrast-induced renal dysfunction: the RAPPID studyChristopher S R Baker, Andrew Wragg, Sanjay Kumar, et al.
Australian and New Zealand Journal of Medicine|December 1, 1996
Hepatitis C genotypes in Australian haemophilia patientsR I Baker, J Smith, J Eikelboom, et al.
Blood|June 22, 2001
Platelet glycoprotein Ibalpha Kozak polymorphism is associated with an increased risk of ischemic strokeR I Baker, J Eikelboom, E Lofthouse, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 13, 2016
Low bleeding rates with increase or maintenance of physical activity in patients treated with recombinant factor VIII Fc fusion protein (rFVIIIFc) in the A-LONG and Kids A-LONG StudiesD V Quon, R Klamroth, R Kulkarni, et al.
Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Collagen platelet receptor polymorphisms integrin alpha2beta1 C807T and GPVI Q317L and risk of ischemic strokeV J Cole, J M Staton, J W Eikelboom, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 25, 2010
Clinical efficacy and safety of the factor VIII/von Willebrand factor concentrate BIOSTATE in patients with von Willebrand's disease: a prospective multi-centre studyS Dunkley, R I Baker, M Pidcock, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2018
Dimeric FcγR ectodomains detect pathogenic anti-platelet factor 4-heparin antibodies in heparin-induced thromobocytopeniaB D Wines, C W Tan, E Duncan, et al.
Journal of Thrombosis and Haemostasis : JTH|May 20, 2008
Compromised ITAM-based platelet receptor function in a patient with immune thrombocytopenic purpuraE E Gardiner, M Al-Tamimi, F-T Mu, et al.
Bone|November 15, 2008
Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic ricketsEmily G Farrow, Siobhan I Davis, Leanne M Ward, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
European Journal of Clinical Nutrition|October 11, 2001
Effects of regular ingestion of black tea on haemostasis and cell adhesion molecules in humansJ M Hodgson, I B Puddey, T A Mori, et al.
Journal of the American College of Cardiology|June 25, 2003
A rapid protocol for the prevention of contrast-induced renal dysfunction: the RAPPID studyChristopher S R Baker, Andrew Wragg, Sanjay Kumar, et al.
Australian and New Zealand Journal of Medicine|December 1, 1996
Hepatitis C genotypes in Australian haemophilia patientsR I Baker, J Smith, J Eikelboom, et al.
Blood|June 22, 2001
Platelet glycoprotein Ibalpha Kozak polymorphism is associated with an increased risk of ischemic strokeR I Baker, J Eikelboom, E Lofthouse, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 13, 2016
Low bleeding rates with increase or maintenance of physical activity in patients treated with recombinant factor VIII Fc fusion protein (rFVIIIFc) in the A-LONG and Kids A-LONG StudiesD V Quon, R Klamroth, R Kulkarni, et al.
Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Collagen platelet receptor polymorphisms integrin alpha2beta1 C807T and GPVI Q317L and risk of ischemic strokeV J Cole, J M Staton, J W Eikelboom, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 25, 2010
Clinical efficacy and safety of the factor VIII/von Willebrand factor concentrate BIOSTATE in patients with von Willebrand's disease: a prospective multi-centre studyS Dunkley, R I Baker, M Pidcock, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2018
Dimeric FcγR ectodomains detect pathogenic anti-platelet factor 4-heparin antibodies in heparin-induced thromobocytopeniaB D Wines, C W Tan, E Duncan, et al.
Journal of Thrombosis and Haemostasis : JTH|May 20, 2008
Compromised ITAM-based platelet receptor function in a patient with immune thrombocytopenic purpuraE E Gardiner, M Al-Tamimi, F-T Mu, et al.
Bone|November 15, 2008
Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic ricketsEmily G Farrow, Siobhan I Davis, Leanne M Ward, et al.
Pageof 5