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Showing results (221-230 of 238) with videos related to

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Experimental Hematology|December 13, 2006
Hematopoietic progenitor cell deficiency in fetuses and children affected by Down's syndromeDenise K Holmes, Nicola Bates, Mary Murray, et al.
British Journal of Haematology|November 18, 2003
Factor V I359T: a novel mutation associated with thrombosis and resistance to activated protein CA D Mumford, J H McVey, C V Morse, et al.
Annals of Hematology|May 8, 2010
Diagnosis and management of chronic ITP: comments from an ICIS expert groupJohn David Grainger, Paula H B Bolton-Maggs, Bertrand Godeau, et al.
Blood|April 18, 2009
A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3Megan S Sutherland, Anthony M Cumming, Mackenzie Bowman, et al.
Journal of Thrombosis and Haemostasis : JTH|January 25, 2023
Tissue factor pathway inhibitor is a potential modifier of bleeding risk in factor XI deficiencyStéphanie E Reitsma, Lori A Holle, Emma G Bouck, et al.
Blood|April 4, 2013
Bleeding manifestations and management of children with persistent and chronic immune thrombocytopenia: data from the Intercontinental Cooperative ITP Study Group (ICIS)Cindy E Neunert, George R Buchanan, Paul Imbach, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 5, 2020
The World Federation of Hemophilia Annual Global Survey 1999-2018Jeffrey S Stonebraker, Paula H B Bolton-Maggs, Mark Brooker, et al.
Blood|August 14, 2008
Severe hemorrhage in children with newly diagnosed immune thrombocytopenic purpuraCindy E Neunert, George R Buchanan, Paul Imbach, et al.
Thrombosis and Haemostasis|November 3, 2006
An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand diseaseAnthony Cumming, Pamela Grundy, Stephen Keeney, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 11, 2004
The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' OrganisationP H B Bolton-Maggs, D J Perry, E A Chalmers, et al.
Pageof 24

Showing results (221-230 of 238) with videos related to

Sort By:
Pageof 24
Experimental Hematology|December 13, 2006
Hematopoietic progenitor cell deficiency in fetuses and children affected by Down's syndromeDenise K Holmes, Nicola Bates, Mary Murray, et al.
British Journal of Haematology|November 18, 2003
Factor V I359T: a novel mutation associated with thrombosis and resistance to activated protein CA D Mumford, J H McVey, C V Morse, et al.
Annals of Hematology|May 8, 2010
Diagnosis and management of chronic ITP: comments from an ICIS expert groupJohn David Grainger, Paula H B Bolton-Maggs, Bertrand Godeau, et al.
Blood|April 18, 2009
A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3Megan S Sutherland, Anthony M Cumming, Mackenzie Bowman, et al.
Journal of Thrombosis and Haemostasis : JTH|January 25, 2023
Tissue factor pathway inhibitor is a potential modifier of bleeding risk in factor XI deficiencyStéphanie E Reitsma, Lori A Holle, Emma G Bouck, et al.
Blood|April 4, 2013
Bleeding manifestations and management of children with persistent and chronic immune thrombocytopenia: data from the Intercontinental Cooperative ITP Study Group (ICIS)Cindy E Neunert, George R Buchanan, Paul Imbach, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 5, 2020
The World Federation of Hemophilia Annual Global Survey 1999-2018Jeffrey S Stonebraker, Paula H B Bolton-Maggs, Mark Brooker, et al.
Blood|August 14, 2008
Severe hemorrhage in children with newly diagnosed immune thrombocytopenic purpuraCindy E Neunert, George R Buchanan, Paul Imbach, et al.
Thrombosis and Haemostasis|November 3, 2006
An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand diseaseAnthony Cumming, Pamela Grundy, Stephen Keeney, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 11, 2004
The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' OrganisationP H B Bolton-Maggs, D J Perry, E A Chalmers, et al.
Pageof 24