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Experimental Hematology
|
December 13, 2006
Hematopoietic progenitor cell deficiency in fetuses and children affected by Down's syndrome
Denise 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 C
A 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 group
John 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 3
Megan 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 deficiency
Stéphanie 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 1999-2018
Jeffrey S Stonebraker, Paula H B Bolton-Maggs, Mark Brooker, et al.
Blood
|
August 14, 2008
Severe hemorrhage in children with newly diagnosed immune thrombocytopenic purpura
Cindy 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 disease
Anthony 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' Organisation
P H B Bolton-Maggs, D J Perry, E A Chalmers, et al.
Page
of 24
Search research articles
Search
Showing results (221-230 of 238) with videos related to
Sort By:
Page
of 24
Experimental Hematology
|
December 13, 2006
Hematopoietic progenitor cell deficiency in fetuses and children affected by Down's syndrome
Denise 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 C
A 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 group
John 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 3
Megan 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 deficiency
Stéphanie 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 1999-2018
Jeffrey S Stonebraker, Paula H B Bolton-Maggs, Mark Brooker, et al.
Blood
|
August 14, 2008
Severe hemorrhage in children with newly diagnosed immune thrombocytopenic purpura
Cindy 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 disease
Anthony 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' Organisation
P H B Bolton-Maggs, D J Perry, E A Chalmers, et al.
Page
of 24