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V Ivaskevicius

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

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Hamostaseologie|February 12, 2011
Haemostasis management of massive bleedingB Pötzsch, V Ivaskevicius
Hamostaseologie|February 8, 2014
Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired formsA Biswas, V Ivaskevicius, A Thomas, et al.
Hamostaseologie|November 11, 2014
Inhibitor development and management in three non-severe haemophilia A patients with T295A variantV Ivaskevicius, G Goldmann, S Horneff, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutationsV Ivaskevicius, J Windyga, B Baran, et al.
Journal of Biochemical and Biophysical Methods|February 17, 2001
Evaluation of DHPLC in the analysis of hemophilia AJ Oldenburg, V Ivaskevicius, S Rost, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 25, 2010
Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiencyV Ivaskevicius, A Biswas, R Loreth, et al.
Hamostaseologie|February 5, 2003
[Significance of mutation analysis in patients with haemophilia A]J Oldenburg, J Schröder, J Graw, et al.
American Journal of Hematology|October 13, 2006
Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusionsE Aygören-Pürsün, I Martinez Saguer, E Rusicke, et al.
British Journal of Haematology|April 12, 2001
Lithuanian haemophilia A and B registry comprising phenotypic and genotypic dataV Ivaskevicius, R Jurgutis, S Rost, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 22, 2007
Molecular characterization of five Italian families with inherited severe factor XIII deficiencyG Castaman, S H Giacomelli, V Ivaskevicius, et al.
Pageof 1

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

Sort By:
Pageof 1
Hamostaseologie|February 12, 2011
Haemostasis management of massive bleedingB Pötzsch, V Ivaskevicius
Hamostaseologie|February 8, 2014
Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired formsA Biswas, V Ivaskevicius, A Thomas, et al.
Hamostaseologie|November 11, 2014
Inhibitor development and management in three non-severe haemophilia A patients with T295A variantV Ivaskevicius, G Goldmann, S Horneff, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutationsV Ivaskevicius, J Windyga, B Baran, et al.
Journal of Biochemical and Biophysical Methods|February 17, 2001
Evaluation of DHPLC in the analysis of hemophilia AJ Oldenburg, V Ivaskevicius, S Rost, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 25, 2010
Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiencyV Ivaskevicius, A Biswas, R Loreth, et al.
Hamostaseologie|February 5, 2003
[Significance of mutation analysis in patients with haemophilia A]J Oldenburg, J Schröder, J Graw, et al.
American Journal of Hematology|October 13, 2006
Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusionsE Aygören-Pürsün, I Martinez Saguer, E Rusicke, et al.
British Journal of Haematology|April 12, 2001
Lithuanian haemophilia A and B registry comprising phenotypic and genotypic dataV Ivaskevicius, R Jurgutis, S Rost, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 22, 2007
Molecular characterization of five Italian families with inherited severe factor XIII deficiencyG Castaman, S H Giacomelli, V Ivaskevicius, et al.
Pageof 1