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I R Peake

Showing results (61-70 of 120) with videos related to

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Thrombosis and Haemostasis|July 10, 1998
A novel mutation in intron K of the PROS1 gene causes aberrant RNA splicing and is a common cause of protein S deficiency in a UK thrombophilia cohortN J Beauchamp, M E Daly, M Makris, et al.
Thrombosis and Haemostasis|September 24, 1999
A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutationsI M Nesbitt, K K Hampton, F E Preston, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 4, 2008
Re-evaluation of three Israeli families initially diagnosed with type 1 von Willebrand disease in light of the ISTH update on von Willebrand factor pathophysiology and classificationS M B Hashemi Soteh, J Anson, A Inbal, et al.
British Journal of Haematology|April 1, 1974
Tissue localization and synthesis of factor-VIII-related antigen in the human foetusE G Tuddenham, A M Shearn, I R Peake, et al.
Lancet (London, England)|September 3, 1994
Rapid two-stage PCR for detecting factor V G1691A mutationN J Beauchamp, M E Daly, P C Cooper, et al.
Thrombosis and Haemostasis|February 18, 1985
The application of a monoclonal antibody to factor VIII related antigen (VIIIRAg) in immunoradiometric assays for factor VIIIJ E Thomas, I R Peake, J C Giddings, et al.
British Journal of Haematology|January 1, 1989
Anti-idiotypes to factor VIII antibodies and their possible role in the pathogenesis and treatment of factor VIII inhibitorsE H Moffat, R A Furlong, A H Dannatt, et al.
Lancet (London, England)|November 2, 1985
Linked and intragenic probes for haemophilia AI R Peake, D P Lillicrap, M B Liddell, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1994
A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and factor IX genes in Thai and Western European populationsA C Goodeve, A Chuansumrit, W Sasanakul, et al.
British Journal of Haematology|June 1, 1990
A mutation adjacent to the beta cleavage site of factor IX (valine 182 to leucine) results in mild haemophilia BmS A Taylor, M B Liddell, I R Peake, et al.
Pageof 12

Showing results (61-70 of 120) with videos related to

Sort By:
Pageof 12
Thrombosis and Haemostasis|July 10, 1998
A novel mutation in intron K of the PROS1 gene causes aberrant RNA splicing and is a common cause of protein S deficiency in a UK thrombophilia cohortN J Beauchamp, M E Daly, M Makris, et al.
Thrombosis and Haemostasis|September 24, 1999
A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutationsI M Nesbitt, K K Hampton, F E Preston, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 4, 2008
Re-evaluation of three Israeli families initially diagnosed with type 1 von Willebrand disease in light of the ISTH update on von Willebrand factor pathophysiology and classificationS M B Hashemi Soteh, J Anson, A Inbal, et al.
British Journal of Haematology|April 1, 1974
Tissue localization and synthesis of factor-VIII-related antigen in the human foetusE G Tuddenham, A M Shearn, I R Peake, et al.
Lancet (London, England)|September 3, 1994
Rapid two-stage PCR for detecting factor V G1691A mutationN J Beauchamp, M E Daly, P C Cooper, et al.
Thrombosis and Haemostasis|February 18, 1985
The application of a monoclonal antibody to factor VIII related antigen (VIIIRAg) in immunoradiometric assays for factor VIIIJ E Thomas, I R Peake, J C Giddings, et al.
British Journal of Haematology|January 1, 1989
Anti-idiotypes to factor VIII antibodies and their possible role in the pathogenesis and treatment of factor VIII inhibitorsE H Moffat, R A Furlong, A H Dannatt, et al.
Lancet (London, England)|November 2, 1985
Linked and intragenic probes for haemophilia AI R Peake, D P Lillicrap, M B Liddell, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1994
A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and factor IX genes in Thai and Western European populationsA C Goodeve, A Chuansumrit, W Sasanakul, et al.
British Journal of Haematology|June 1, 1990
A mutation adjacent to the beta cleavage site of factor IX (valine 182 to leucine) results in mild haemophilia BmS A Taylor, M B Liddell, I R Peake, et al.
Pageof 12