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K Schallmoser

Showing results (1-10 of 20) with videos related to

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Wiener Medizinische Wochenschrift (1946)|July 17, 1999
[Statins--attaining goal values--with reference to recent studies]H Toplak, K Schallmoser, A DeCampo
Transfusion Medicine (Oxford, England)|March 18, 2014
Therapeutic red blood cell exchange in a child with sickle cell anaemia using the Spectra Optia® apheresis systemS Sipurzynski-Budrass, P Sovinz, G Lanzer, et al.
Atherosclerosis|July 27, 2001
A novel splice-site mutation in intron 7 causes more severe hypercholesterolemia than a combined FH-FDB defectA deCampo, K Schallmoser, H Schmidt, et al.
Vox Sanguinis|October 22, 2014
T-cell death, phosphatidylserine exposure and reduced proliferation rate to validate extracorporeal photochemotherapyD Schmid, C Grabmer, D Streif, et al.
Vox Sanguinis|August 16, 2006
Delayed detectability of anti-HPA-3a by the MAIPA assay in a severe neonatal alloimmune thrombocytopenia, but successful transfusion of incompatible donor platelets: a case reportK Schallmoser, J Kutschera, S Macher, et al.
Lupus|September 1, 2006
Specificities of platelet autoantibodies and platelet activation in lupus anticoagulant patients: a relation to their history of thromboembolic diseaseK Schallmoser, C Rosin, R Vormittag, et al.
Atherosclerosis|September 21, 2000
C242T polymorphism of the p22 phox gene is not associated with peripheral arterial occlusive diseaseW Renner, K Schallmoser, P Gallippi, et al.
Vox Sanguinis|November 3, 2005
Severe thrombocytopenia due to host-derived anti-HPA-1a after non-myeloablative allogeneic haematopoietic stem cell transplantation for multiple myeloma: a case reportS Macher, K Schallmoser, P B Staber, et al.
Wiener Medizinische Wochenschrift (1946)|January 1, 1993
[Eating behavior of patients with metabolic diseases and metabolically healthy probands in Austria. Results of a questionnaire survey at the Graz Autumn Fair 1991]M Schumacher, B Eber, K Schallmoser, et al.
European Journal of Clinical Investigation|March 19, 2003
Lack of association of the Glu298Asp polymorphism of endothelial nitric oxide synthase with manifest coronary artery disease, carotid atherosclerosis and forearm vascular reactivity in two Austrian populationsI Schmoelzer, W Renner, B Paulweber, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Wiener Medizinische Wochenschrift (1946)|July 17, 1999
[Statins--attaining goal values--with reference to recent studies]H Toplak, K Schallmoser, A DeCampo
Transfusion Medicine (Oxford, England)|March 18, 2014
Therapeutic red blood cell exchange in a child with sickle cell anaemia using the Spectra Optia® apheresis systemS Sipurzynski-Budrass, P Sovinz, G Lanzer, et al.
Atherosclerosis|July 27, 2001
A novel splice-site mutation in intron 7 causes more severe hypercholesterolemia than a combined FH-FDB defectA deCampo, K Schallmoser, H Schmidt, et al.
Vox Sanguinis|October 22, 2014
T-cell death, phosphatidylserine exposure and reduced proliferation rate to validate extracorporeal photochemotherapyD Schmid, C Grabmer, D Streif, et al.
Vox Sanguinis|August 16, 2006
Delayed detectability of anti-HPA-3a by the MAIPA assay in a severe neonatal alloimmune thrombocytopenia, but successful transfusion of incompatible donor platelets: a case reportK Schallmoser, J Kutschera, S Macher, et al.
Lupus|September 1, 2006
Specificities of platelet autoantibodies and platelet activation in lupus anticoagulant patients: a relation to their history of thromboembolic diseaseK Schallmoser, C Rosin, R Vormittag, et al.
Atherosclerosis|September 21, 2000
C242T polymorphism of the p22 phox gene is not associated with peripheral arterial occlusive diseaseW Renner, K Schallmoser, P Gallippi, et al.
Vox Sanguinis|November 3, 2005
Severe thrombocytopenia due to host-derived anti-HPA-1a after non-myeloablative allogeneic haematopoietic stem cell transplantation for multiple myeloma: a case reportS Macher, K Schallmoser, P B Staber, et al.
Wiener Medizinische Wochenschrift (1946)|January 1, 1993
[Eating behavior of patients with metabolic diseases and metabolically healthy probands in Austria. Results of a questionnaire survey at the Graz Autumn Fair 1991]M Schumacher, B Eber, K Schallmoser, et al.
European Journal of Clinical Investigation|March 19, 2003
Lack of association of the Glu298Asp polymorphism of endothelial nitric oxide synthase with manifest coronary artery disease, carotid atherosclerosis and forearm vascular reactivity in two Austrian populationsI Schmoelzer, W Renner, B Paulweber, et al.
Pageof 2