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T P Baglin

Showing results (31-40 of 85) with videos related to

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British Journal of Haematology|August 1, 1988
A reversible defect of platelet PDGF content in myeloproliferative disordersT P Baglin, S M Price, B J Boughton
Journal of Thrombosis and Haemostasis : JTH|October 16, 2015
Discovery and characterization of an antibody directed against exosite I of thrombinT P Baglin, J Langdown, R Frasson, et al.
Lancet (London, England)|February 20, 1993
Thrombin generation and myocardial infarction during infusion of tissue-plasminogen activatorT P Baglin, R Luddington, I Jennings, et al.
Thrombosis and Haemostasis|April 1, 2000
The C536T transition in the tissue factor pathway inhibitor gene is not a common cause of venous thromboembolic disease in the UK populationG D Evans, J Langdown, K Brown, et al.
Journal of Thrombosis and Haemostasis : JTH|August 17, 2005
Is there a true difference in recurrence rate of deep venous thrombosis between men and women?A van Hylckama Vlieg, C A Baglin, T P Baglin
Platelets|January 1, 1997
Heparin-induced thrombocytopenia: an under-diagnosed syndrome? Proceedings of a workshop held in London on 1 November 1996. Consensus overviewJ Amiral, T P Baglin, H N Magnani, et al.
British Journal of Haematology|May 1, 1995
Haemoglobin Dhofar is linked to the codon 29 C-->T (IVS-1 nt-3) splice mutation which causes beta+ thalassaemiaD Williamson, K P Brown, J V Langdown, et al.
Thrombosis and Haemostasis|June 1, 1997
Relative risk of pulmonary embolism and deep vein thrombosis in association with the factor V Leiden mutation in a United Kingdom populationT P Baglin, K Brown, D Williamson, et al.
Hemoglobin|January 7, 1998
Mild thalassemia intermedia resulting from a new insertion/frameshift mutation in the beta-globin geneD Williamson, K P Brown, J V Langdown, et al.
Blood|January 15, 1998
Atherogenic lipoproteins support assembly of the prothrombinase complex and thrombin generation: modulation by oxidation and vitamin ES Rota, N A McWilliam, T P Baglin, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
British Journal of Haematology|August 1, 1988
A reversible defect of platelet PDGF content in myeloproliferative disordersT P Baglin, S M Price, B J Boughton
Journal of Thrombosis and Haemostasis : JTH|October 16, 2015
Discovery and characterization of an antibody directed against exosite I of thrombinT P Baglin, J Langdown, R Frasson, et al.
Lancet (London, England)|February 20, 1993
Thrombin generation and myocardial infarction during infusion of tissue-plasminogen activatorT P Baglin, R Luddington, I Jennings, et al.
Thrombosis and Haemostasis|April 1, 2000
The C536T transition in the tissue factor pathway inhibitor gene is not a common cause of venous thromboembolic disease in the UK populationG D Evans, J Langdown, K Brown, et al.
Journal of Thrombosis and Haemostasis : JTH|August 17, 2005
Is there a true difference in recurrence rate of deep venous thrombosis between men and women?A van Hylckama Vlieg, C A Baglin, T P Baglin
Platelets|January 1, 1997
Heparin-induced thrombocytopenia: an under-diagnosed syndrome? Proceedings of a workshop held in London on 1 November 1996. Consensus overviewJ Amiral, T P Baglin, H N Magnani, et al.
British Journal of Haematology|May 1, 1995
Haemoglobin Dhofar is linked to the codon 29 C-->T (IVS-1 nt-3) splice mutation which causes beta+ thalassaemiaD Williamson, K P Brown, J V Langdown, et al.
Thrombosis and Haemostasis|June 1, 1997
Relative risk of pulmonary embolism and deep vein thrombosis in association with the factor V Leiden mutation in a United Kingdom populationT P Baglin, K Brown, D Williamson, et al.
Hemoglobin|January 7, 1998
Mild thalassemia intermedia resulting from a new insertion/frameshift mutation in the beta-globin geneD Williamson, K P Brown, J V Langdown, et al.
Blood|January 15, 1998
Atherogenic lipoproteins support assembly of the prothrombinase complex and thrombin generation: modulation by oxidation and vitamin ES Rota, N A McWilliam, T P Baglin, et al.
Pageof 9