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D Lillicrap

Showing results (81-90 of 132) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|August 3, 2017
Minimal dataset for post-registration surveillance of new drugs in hemophilia: communication from the SSC of the ISTHF Peyvandi, M Makris, P Collins, et al.
British Journal of Haematology|January 1, 1995
Rapid genotype analysis in type 2B von Willebrand's disease using a universal heteroduplex generatorN Wood, G R Standen, E W Murray, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 22, 2012
Bleeding disorders, menorrhagia and iron deficiency: impacts on health-related quality of lifeC Rae, W Furlong, J Horsman, et al.
Environmental Toxicology and Chemistry|April 24, 2007
Evaluation of the reproductive effects of tamoxifen citrate in partial and full life-cycle studies using fathead minnows (Pimephales promelas)Tim D Williams, John E Caunter, Adam D Lillicrap, et al.
Journal of Thrombosis and Haemostasis : JTH|July 15, 2010
ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disordersF Rodeghiero, A Tosetto, T Abshire, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 20, 2009
Non-neutralizing anti-FVIII antibodies: different binding specificity to different recombinant FVIII concentratesA M Vincent, D Lillicrap, A Boulanger, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 14, 2005
Can activated recombinant factor VII be used to postpone the exposure of infants to factor VIII until after 2 years of age?G E Rivard, D Lillicrap, M C Poon, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 9, 2007
Different clinical phenotype in triplets with haemophilia AC Barnes, V Blanchette, D Lillicrap, et al.
Journal of Thrombosis and Haemostasis : JTH|October 2, 2008
Reduction of the immune response to factor VIII mediated through tolerogenic factor VIII presentation by immature dendritic cellsM Qadura, M Othman, B Waters, et al.
British Journal of Haematology|December 1, 1991
Recurring mutations at CpG dinucleotides in the region of the von Willebrand factor gene encoding the glycoprotein Ib binding domain, in patients with type IIB von Willebrand's diseaseD Lillicrap, E W Murray, K Benford, et al.
Pageof 14

Showing results (81-90 of 132) with videos related to

Sort By:
Pageof 14
Journal of Thrombosis and Haemostasis : JTH|August 3, 2017
Minimal dataset for post-registration surveillance of new drugs in hemophilia: communication from the SSC of the ISTHF Peyvandi, M Makris, P Collins, et al.
British Journal of Haematology|January 1, 1995
Rapid genotype analysis in type 2B von Willebrand's disease using a universal heteroduplex generatorN Wood, G R Standen, E W Murray, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 22, 2012
Bleeding disorders, menorrhagia and iron deficiency: impacts on health-related quality of lifeC Rae, W Furlong, J Horsman, et al.
Environmental Toxicology and Chemistry|April 24, 2007
Evaluation of the reproductive effects of tamoxifen citrate in partial and full life-cycle studies using fathead minnows (Pimephales promelas)Tim D Williams, John E Caunter, Adam D Lillicrap, et al.
Journal of Thrombosis and Haemostasis : JTH|July 15, 2010
ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disordersF Rodeghiero, A Tosetto, T Abshire, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 20, 2009
Non-neutralizing anti-FVIII antibodies: different binding specificity to different recombinant FVIII concentratesA M Vincent, D Lillicrap, A Boulanger, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 14, 2005
Can activated recombinant factor VII be used to postpone the exposure of infants to factor VIII until after 2 years of age?G E Rivard, D Lillicrap, M C Poon, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 9, 2007
Different clinical phenotype in triplets with haemophilia AC Barnes, V Blanchette, D Lillicrap, et al.
Journal of Thrombosis and Haemostasis : JTH|October 2, 2008
Reduction of the immune response to factor VIII mediated through tolerogenic factor VIII presentation by immature dendritic cellsM Qadura, M Othman, B Waters, et al.
British Journal of Haematology|December 1, 1991
Recurring mutations at CpG dinucleotides in the region of the von Willebrand factor gene encoding the glycoprotein Ib binding domain, in patients with type IIB von Willebrand's diseaseD Lillicrap, E W Murray, K Benford, et al.
Pageof 14