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D Lillicrap

Showing results (101-110 of 132) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|August 30, 2008
Orthopaedic surgery in haemophilia patients with inhibitors: a practical guide to haemostatic, surgical and rehabilitative careJ M Teitel, M Carcao, D Lillicrap, et al.
Journal of Thrombosis and Haemostasis : JTH|October 10, 2007
The effect of exercise on von Willebrand factor and ADAMTS-13 in individuals with type 1 and type 2B von Willebrand diseaseJ Stakiw, M Bowman, C Hegadorn, et al.
Journal of Thrombosis and Haemostasis : JTH|April 26, 2006
Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD studyP D James, A D Paterson, C Notley, et al.
Journal of Thrombosis and Haemostasis : JTH|September 3, 2016
Histones link inflammation and thrombosis through the induction of Weibel-Palade body exocytosisA Michels, S Albánez, J Mewburn, et al.
Journal of Thrombosis and Haemostasis : JTH|June 30, 2011
Expanded phenotype-genotype correlations in a pediatric population with type 1 von Willebrand diseaseJ D Robertson, P R Yenson, M L Rand, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 11, 2006
Ethical issues in haemophiliaD DiMichele, A Chuansumrit, A J London, et al.
British Journal of Haematology|June 1, 1990
A past mutation at isoleucine 397 is now a common cause of moderate/mild haemophilia BC D Bottema, D D Koeberl, R P Ketterling, et al.
Journal of Thrombosis and Haemostasis : JTH|February 9, 2010
Quantitation of bleeding symptoms in children with von Willebrand disease: use of a standardized pediatric bleeding questionnaireT T Biss, V S Blanchette, D S Clark, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 2, 2018
World bleeding disorders registry: The pilot studyD Coffin, C Herr, J O'Hara, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 14, 2004
von Willebrand disease: laboratory aspects of diagnosis and treatmentE J Favaloro, D Lillicrap, M A Lazzari, et al.
Pageof 14

Showing results (101-110 of 132) with videos related to

Sort By:
Pageof 14
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 30, 2008
Orthopaedic surgery in haemophilia patients with inhibitors: a practical guide to haemostatic, surgical and rehabilitative careJ M Teitel, M Carcao, D Lillicrap, et al.
Journal of Thrombosis and Haemostasis : JTH|October 10, 2007
The effect of exercise on von Willebrand factor and ADAMTS-13 in individuals with type 1 and type 2B von Willebrand diseaseJ Stakiw, M Bowman, C Hegadorn, et al.
Journal of Thrombosis and Haemostasis : JTH|April 26, 2006
Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD studyP D James, A D Paterson, C Notley, et al.
Journal of Thrombosis and Haemostasis : JTH|September 3, 2016
Histones link inflammation and thrombosis through the induction of Weibel-Palade body exocytosisA Michels, S Albánez, J Mewburn, et al.
Journal of Thrombosis and Haemostasis : JTH|June 30, 2011
Expanded phenotype-genotype correlations in a pediatric population with type 1 von Willebrand diseaseJ D Robertson, P R Yenson, M L Rand, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 11, 2006
Ethical issues in haemophiliaD DiMichele, A Chuansumrit, A J London, et al.
British Journal of Haematology|June 1, 1990
A past mutation at isoleucine 397 is now a common cause of moderate/mild haemophilia BC D Bottema, D D Koeberl, R P Ketterling, et al.
Journal of Thrombosis and Haemostasis : JTH|February 9, 2010
Quantitation of bleeding symptoms in children with von Willebrand disease: use of a standardized pediatric bleeding questionnaireT T Biss, V S Blanchette, D S Clark, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 2, 2018
World bleeding disorders registry: The pilot studyD Coffin, C Herr, J O'Hara, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 14, 2004
von Willebrand disease: laboratory aspects of diagnosis and treatmentE J Favaloro, D Lillicrap, M A Lazzari, et al.
Pageof 14