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Hamostaseologie
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February 12, 2011
Haemostasis management of massive bleeding
B Pötzsch, V Ivaskevicius
Hamostaseologie
|
February 8, 2014
Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms
A Biswas, V Ivaskevicius, A Thomas, et al.
Hamostaseologie
|
November 11, 2014
Inhibitor development and management in three non-severe haemophilia A patients with T295A variant
V 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 mutations
V Ivaskevicius, J Windyga, B Baran, et al.
Journal of Biochemical and Biophysical Methods
|
February 17, 2001
Evaluation of DHPLC in the analysis of hemophilia A
J 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 deficiency
V 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 infusions
E 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 data
V 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 deficiency
G Castaman, S H Giacomelli, V Ivaskevicius, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Hamostaseologie
|
February 12, 2011
Haemostasis management of massive bleeding
B Pötzsch, V Ivaskevicius
Hamostaseologie
|
February 8, 2014
Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms
A Biswas, V Ivaskevicius, A Thomas, et al.
Hamostaseologie
|
November 11, 2014
Inhibitor development and management in three non-severe haemophilia A patients with T295A variant
V 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 mutations
V Ivaskevicius, J Windyga, B Baran, et al.
Journal of Biochemical and Biophysical Methods
|
February 17, 2001
Evaluation of DHPLC in the analysis of hemophilia A
J 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 deficiency
V 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 infusions
E 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 data
V 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 deficiency
G Castaman, S H Giacomelli, V Ivaskevicius, et al.
Page
of 1