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I Peake

Showing results (11-20 of 25) with videos related to

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Blood|April 15, 1996
A novel DNA inversion causing severe hemophilia AJ A Naylor, P Nicholson, Goodeve Anne, et al.
Anaesthesia and Intensive Care|May 15, 2012
Assessing the performance of a continuous infusion for potassium supplementation in the critically illR P Chalwin, J L Moran, S I Peake, et al.
Human Mutation|September 30, 1999
A study of Wilson disease mutations in BritainD Curtis, M Durkie, P Balac (Morris), et al.
British Journal of Haematology|November 11, 1999
c-kit proto-oncogene exon 8 in-frame deletion plus insertion mutations in acute myeloid leukaemiaM Gari, A Goodeve, G Wilson, et al.
Blood|September 25, 1998
Late relapsing childhood lymphoblastic leukemiaA Vora, L Frost, A Goodeve, et al.
British Journal of Haematology|August 1, 1995
A chromogenic assay for activated protein C resistanceK Váradi, B Moritz, H Lang, et al.
American Journal of Human Genetics|June 19, 2001
Somatic mosaicism in hemophilia A: a fairly common eventM Leuer, J Oldenburg, J M Lavergne, et al.
Journal of Thrombosis and Haemostasis : JTH|May 25, 2010
von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levelsN Hickson, D Hampshire, P Winship, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 22, 2012
von Willebrand's disease: a report from a meeting in the Åland islandsE Berntorp, I Peake, U Budde, et al.
Journal of Thrombosis and Haemostasis : JTH|April 26, 2006
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD)A Tosetto, F Rodeghiero, G Castaman, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Blood|April 15, 1996
A novel DNA inversion causing severe hemophilia AJ A Naylor, P Nicholson, Goodeve Anne, et al.
Anaesthesia and Intensive Care|May 15, 2012
Assessing the performance of a continuous infusion for potassium supplementation in the critically illR P Chalwin, J L Moran, S I Peake, et al.
Human Mutation|September 30, 1999
A study of Wilson disease mutations in BritainD Curtis, M Durkie, P Balac (Morris), et al.
British Journal of Haematology|November 11, 1999
c-kit proto-oncogene exon 8 in-frame deletion plus insertion mutations in acute myeloid leukaemiaM Gari, A Goodeve, G Wilson, et al.
Blood|September 25, 1998
Late relapsing childhood lymphoblastic leukemiaA Vora, L Frost, A Goodeve, et al.
British Journal of Haematology|August 1, 1995
A chromogenic assay for activated protein C resistanceK Váradi, B Moritz, H Lang, et al.
American Journal of Human Genetics|June 19, 2001
Somatic mosaicism in hemophilia A: a fairly common eventM Leuer, J Oldenburg, J M Lavergne, et al.
Journal of Thrombosis and Haemostasis : JTH|May 25, 2010
von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levelsN Hickson, D Hampshire, P Winship, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 22, 2012
von Willebrand's disease: a report from a meeting in the Åland islandsE Berntorp, I Peake, U Budde, et al.
Journal of Thrombosis and Haemostasis : JTH|April 26, 2006
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD)A Tosetto, F Rodeghiero, G Castaman, et al.
Pageof 3