M Halbmayer - JoVE Visualize

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Coronary Artery Disease|May 1, 1994

Prevalence of factor XII (Hageman factor) deficiency among 426 patients with coronary heart disease awaiting cardiac surgeryW M Halbmayer, A Haushofer, J Radek, et al.

Coronary Artery Disease|May 1, 1995

Platelet size, fibrinogen and lipoprotein(a) in coronary heart diseaseW M Halbmayer, A Haushofer, J Radek, et al.

Journal of Thrombosis and Haemostasis : JTH|April 26, 2006

Prediction of recurrent venous thromboembolism by the activated partial thromboplastin timeG Hron, S Eichinger, A Weltermann, et al.

Thrombosis and Haemostasis|January 1, 1994

The prevalence of moderate and severe FXII (Hageman factor) deficiency among the normal population: evaluation of the incidence of FXII deficiency among 300 healthy blood donorsW M Halbmayer, A Haushofer, R Schön, et al.

Zeitschrift Fur Kardiologie|January 1, 1995

[Changes in antithrombin III, prothrombin fragment 1 + 2 and thrombin-antithrombin III complex following implantation of a coronary Palmaz-Schatz stent]M Dittel, A Haushofer, R Spiel, et al.

Thrombosis and Haemostasis|February 12, 1991

C1-esterase inhibitor in uncomplicated pregnancy and mild and moderate preeclampsiaW M Halbmayer, P Hopmeier, C Mannhalter, et al.

Wiener Klinische Wochenschrift|July 13, 1990

[A simple test for the monitoring of plasma anti-XA activity of patients following subcutaneous administration of enoxaparin]W M Halbmayer, C Feichtinger, T Schwarz, et al.

Deutsche Medizinische Wochenschrift (1946)|October 29, 1993

[Recurrent venous thromboses in hypoplasia of the vena cava inferior and factor XII deficiency]W M Halbmayer, J Radek, P Duschet, et al.

The Clinical Investigator|July 1, 1994

High-dose intravenous melphalan in a patient with multiple myeloma and oliguric renal failureM Pecherstorfer, I Zimmer-Roth, S Weidinger, 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.

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Showing results (21-30 of 33) with videos related to

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Coronary Artery Disease|May 1, 1994

Prevalence of factor XII (Hageman factor) deficiency among 426 patients with coronary heart disease awaiting cardiac surgeryW M Halbmayer, A Haushofer, J Radek, et al.

Coronary Artery Disease|May 1, 1995

Platelet size, fibrinogen and lipoprotein(a) in coronary heart diseaseW M Halbmayer, A Haushofer, J Radek, et al.

Journal of Thrombosis and Haemostasis : JTH|April 26, 2006

Prediction of recurrent venous thromboembolism by the activated partial thromboplastin timeG Hron, S Eichinger, A Weltermann, et al.

Thrombosis and Haemostasis|January 1, 1994

The prevalence of moderate and severe FXII (Hageman factor) deficiency among the normal population: evaluation of the incidence of FXII deficiency among 300 healthy blood donorsW M Halbmayer, A Haushofer, R Schön, et al.

Zeitschrift Fur Kardiologie|January 1, 1995

[Changes in antithrombin III, prothrombin fragment 1 + 2 and thrombin-antithrombin III complex following implantation of a coronary Palmaz-Schatz stent]M Dittel, A Haushofer, R Spiel, et al.

Thrombosis and Haemostasis|February 12, 1991

C1-esterase inhibitor in uncomplicated pregnancy and mild and moderate preeclampsiaW M Halbmayer, P Hopmeier, C Mannhalter, et al.

Wiener Klinische Wochenschrift|July 13, 1990

[A simple test for the monitoring of plasma anti-XA activity of patients following subcutaneous administration of enoxaparin]W M Halbmayer, C Feichtinger, T Schwarz, et al.

Deutsche Medizinische Wochenschrift (1946)|October 29, 1993

[Recurrent venous thromboses in hypoplasia of the vena cava inferior and factor XII deficiency]W M Halbmayer, J Radek, P Duschet, et al.

The Clinical Investigator|July 1, 1994

High-dose intravenous melphalan in a patient with multiple myeloma and oliguric renal failureM Pecherstorfer, I Zimmer-Roth, S Weidinger, 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.

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