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C Mannhalter

Showing results (101-110 of 184) with videos related to

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British Journal of Haematology|July 1, 1996
Multiplex PCR for rapid detection of T-cell receptor-gamma chain gene rearrangements in patients with lymphoproliferative diseasesM Födinger, H Buchmayer, I Schwarzinger, et al.
Journal of Endovascular Therapy : an Official Journal of the International Society of Endovascular Specialists|November 23, 2001
Heme oxygenase-1 gene promoter microsatellite polymorphism is associated with restenosis after percutaneous transluminal angioplastyM Exner, M Schillinger, E Minar, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 1, 1996
Resistance to activated protein C (APC): mutation at Arg506 of coagulation factor V and vascular access thrombosis in haemodialysis patientsM Födinger, C Mannhalter, I Pabinger, et al.
European Journal of Neurology|September 21, 2007
Polymorphisms in the coagulation factor VII gene and risk of primary intracerebral hemorrhageS Greisenegger, M Weber, M Funk, et al.
Thrombosis Research|October 23, 1997
Evaluation of a new screening assay ProC Global for identification of defects in the protein C/protein S anticoagulant pathwayK Ruzicka, S Kapiotis, P Quehenberger, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 7, 1999
No evidence for an increased risk of venous thrombosis in patients with factor V Leiden by the homozygous 677 C to T mutation in the methylenetetrahydrofolate-reductase geneC Rintelen, C Mannhalter, K Lechner, et al.
Journal of Thrombosis and Haemostasis : JTH|November 11, 2014
Factor V Leiden mutation increases the risk for venous thromboembolism in cancer patients - results from the Vienna Cancer And Thrombosis Study (CATS)I Pabinger, C Ay, D Dunkler, et al.
Blood|August 8, 1998
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin geneA Zivelin, N Rosenberg, S Faier, et al.
European Journal of Haematology|December 12, 2001
Impact of the factor II: G20210A variant on the risk of venous thromboembolism in relatives from families with the factor V: R506Q mutationC Rintelen, I Pabinger, P Bettelheim, et al.
Thrombosis Research|February 9, 1999
C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: a case-control studyW Lalouschek, S Aull, W Serles, et al.
Pageof 19

Showing results (101-110 of 184) with videos related to

Sort By:
Pageof 19
British Journal of Haematology|July 1, 1996
Multiplex PCR for rapid detection of T-cell receptor-gamma chain gene rearrangements in patients with lymphoproliferative diseasesM Födinger, H Buchmayer, I Schwarzinger, et al.
Journal of Endovascular Therapy : an Official Journal of the International Society of Endovascular Specialists|November 23, 2001
Heme oxygenase-1 gene promoter microsatellite polymorphism is associated with restenosis after percutaneous transluminal angioplastyM Exner, M Schillinger, E Minar, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 1, 1996
Resistance to activated protein C (APC): mutation at Arg506 of coagulation factor V and vascular access thrombosis in haemodialysis patientsM Födinger, C Mannhalter, I Pabinger, et al.
European Journal of Neurology|September 21, 2007
Polymorphisms in the coagulation factor VII gene and risk of primary intracerebral hemorrhageS Greisenegger, M Weber, M Funk, et al.
Thrombosis Research|October 23, 1997
Evaluation of a new screening assay ProC Global for identification of defects in the protein C/protein S anticoagulant pathwayK Ruzicka, S Kapiotis, P Quehenberger, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 7, 1999
No evidence for an increased risk of venous thrombosis in patients with factor V Leiden by the homozygous 677 C to T mutation in the methylenetetrahydrofolate-reductase geneC Rintelen, C Mannhalter, K Lechner, et al.
Journal of Thrombosis and Haemostasis : JTH|November 11, 2014
Factor V Leiden mutation increases the risk for venous thromboembolism in cancer patients - results from the Vienna Cancer And Thrombosis Study (CATS)I Pabinger, C Ay, D Dunkler, et al.
Blood|August 8, 1998
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin geneA Zivelin, N Rosenberg, S Faier, et al.
European Journal of Haematology|December 12, 2001
Impact of the factor II: G20210A variant on the risk of venous thromboembolism in relatives from families with the factor V: R506Q mutationC Rintelen, I Pabinger, P Bettelheim, et al.
Thrombosis Research|February 9, 1999
C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: a case-control studyW Lalouschek, S Aull, W Serles, et al.
Pageof 19