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I Pabinger

Showing results (121-130 of 211) with videos related to

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The Journal of Cardiovascular Surgery|May 1, 1990
Four year follow-up of the Duromedics Edwards bileaflet valve prosthesesA Moritz, W Klepetko, G Khünl-Brady, et al.
Journal of Thrombosis and Haemostasis : JTH|September 11, 2014
Prevention of venous thromboembolism in cancer outpatients: guidance from the SSC of the ISTHA A Khorana, H-M Otten, J I Zwicker, et al.
Blut|November 1, 1990
Hemostatic and fibrinolytic parameters in patients with acute myeloid leukemia: activation of blood coagulation, fibrinolysis and unspecific proteolysisW Speiser, I Pabinger-Fasching, P A Kyrle, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 23, 2001
Preeclampsia and fetal loss in women with a history of venous thromboembolismI Pabinger, H Grafenhofer, A Kaider, et al.
Kidney International|August 1, 1997
Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patientsM Födinger, C Mannhalter, G Wölfl, et al.
Haemostasis|January 1, 1990
1-Deamino-8-D-arginine vasopressin in the treatment of non-haemophilic patients with acquired factor VIII inhibitorM Muhm, N Grois, P Kier, et al.
Journal of the Neurological Sciences|April 30, 1998
677C to T mutation in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene and plasma homocyst(e)ine levels in patients with TIA or minor strokeW Lalouschek, S Aull, L Korninger, et al.
Thrombosis Research|May 11, 2016
PO-63 - Exhausted platelets in cancer patients with high risk of venous thromboembolism and poor prognosisJ Riedl, A Kaider, C Marosi, et al.
Journal of Thrombosis and Haemostasis : JTH|October 7, 2015
International Society on Thrombosis and Haemostasis core curriculum project: core competencies in clinical thrombosis and hemostasisC McLintock, I Pabinger, K A Bauer, et al.
British Journal of Haematology|December 31, 1997
A hitherto unknown splice site defect in the protein S gene (PROS1): the mutation results in allelic exclusion and causes type I and type III protein S deficiencyS Mustafa, I Pabinger, K Vàradi, et al.
Pageof 22

Showing results (121-130 of 211) with videos related to

Sort By:
Pageof 22
The Journal of Cardiovascular Surgery|May 1, 1990
Four year follow-up of the Duromedics Edwards bileaflet valve prosthesesA Moritz, W Klepetko, G Khünl-Brady, et al.
Journal of Thrombosis and Haemostasis : JTH|September 11, 2014
Prevention of venous thromboembolism in cancer outpatients: guidance from the SSC of the ISTHA A Khorana, H-M Otten, J I Zwicker, et al.
Blut|November 1, 1990
Hemostatic and fibrinolytic parameters in patients with acute myeloid leukemia: activation of blood coagulation, fibrinolysis and unspecific proteolysisW Speiser, I Pabinger-Fasching, P A Kyrle, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 23, 2001
Preeclampsia and fetal loss in women with a history of venous thromboembolismI Pabinger, H Grafenhofer, A Kaider, et al.
Kidney International|August 1, 1997
Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patientsM Födinger, C Mannhalter, G Wölfl, et al.
Haemostasis|January 1, 1990
1-Deamino-8-D-arginine vasopressin in the treatment of non-haemophilic patients with acquired factor VIII inhibitorM Muhm, N Grois, P Kier, et al.
Journal of the Neurological Sciences|April 30, 1998
677C to T mutation in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene and plasma homocyst(e)ine levels in patients with TIA or minor strokeW Lalouschek, S Aull, L Korninger, et al.
Thrombosis Research|May 11, 2016
PO-63 - Exhausted platelets in cancer patients with high risk of venous thromboembolism and poor prognosisJ Riedl, A Kaider, C Marosi, et al.
Journal of Thrombosis and Haemostasis : JTH|October 7, 2015
International Society on Thrombosis and Haemostasis core curriculum project: core competencies in clinical thrombosis and hemostasisC McLintock, I Pabinger, K A Bauer, et al.
British Journal of Haematology|December 31, 1997
A hitherto unknown splice site defect in the protein S gene (PROS1): the mutation results in allelic exclusion and causes type I and type III protein S deficiencyS Mustafa, I Pabinger, K Vàradi, et al.
Pageof 22