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C Mannhalter

Showing results (111-120 of 184) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|September 18, 2009
Determinants of factor VIII plasma levels in carriers of haemophilia A and in control womenC Ay, K Thom, F Abu-Hamdeh, et al.
Blood|May 29, 2000
Follicular lymphomas' BCL-2/IgH junctions contain templated nucleotide insertions: novel insights into the mechanism of t(14;18) translocationU Jäger, S Böcskör, T Le, et al.
Thrombosis Research|March 15, 2001
A common C-->T polymorphism at nt 46 in the promoter region of coagulation factor XII is associated with decreased factor XII activityG Endler, M Exner, C Mannhalter, 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.
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.
British Journal of Haematology|October 1, 1994
PML-RAR alpha PCR positivity in the bone marrow of patients with APL precedes haematological relapse by 2-3 monthsL Korninger, P Knöbl, K Laczika, 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.
Annals of Hematology|October 1, 1991
Detection of engraftment and mixed chimerism following bone marrow transplantation using PCR amplification of a highly variable region-variable number of tandem repeats (VNTR) in the von Willebrand factor geneA Gaiger, C Mannhalter, W Hinterberger, 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.
Thrombosis and Haemostasis|September 9, 2011
The role of fibrinogen plasma levels, the -455G>A fibrinogen and the factor XIII A subunit (FXIII-A) Val34Leu polymorphism in cancer-associated venous thrombosisV Tiedje, D Dunkler, C Ay, et al.
Pageof 19

Showing results (111-120 of 184) with videos related to

Sort By:
Pageof 19
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 18, 2009
Determinants of factor VIII plasma levels in carriers of haemophilia A and in control womenC Ay, K Thom, F Abu-Hamdeh, et al.
Blood|May 29, 2000
Follicular lymphomas' BCL-2/IgH junctions contain templated nucleotide insertions: novel insights into the mechanism of t(14;18) translocationU Jäger, S Böcskör, T Le, et al.
Thrombosis Research|March 15, 2001
A common C-->T polymorphism at nt 46 in the promoter region of coagulation factor XII is associated with decreased factor XII activityG Endler, M Exner, C Mannhalter, 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.
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.
British Journal of Haematology|October 1, 1994
PML-RAR alpha PCR positivity in the bone marrow of patients with APL precedes haematological relapse by 2-3 monthsL Korninger, P Knöbl, K Laczika, 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.
Annals of Hematology|October 1, 1991
Detection of engraftment and mixed chimerism following bone marrow transplantation using PCR amplification of a highly variable region-variable number of tandem repeats (VNTR) in the von Willebrand factor geneA Gaiger, C Mannhalter, W Hinterberger, 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.
Thrombosis and Haemostasis|September 9, 2011
The role of fibrinogen plasma levels, the -455G>A fibrinogen and the factor XIII A subunit (FXIII-A) Val34Leu polymorphism in cancer-associated venous thrombosisV Tiedje, D Dunkler, C Ay, et al.
Pageof 19