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R Liesner

Showing results (11-20 of 64) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|May 1, 2018
Prophylactic treatment of bleeding episodes in children <12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high-purity plasma-derived factor X (pdFX) concentrateR Liesner, C Akanezi, M Norton, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 1, 2000
The use of recombinant factor VIIa in a patient with severe Glanzmann's thrombasthenia to facilitate insertion of a Port-a-CathP Ancliff, R Liesner, K Khair, et al.
Pediatric Hematology and Oncology|November 24, 2004
Subcutaneous administration of protein C concentrateM Mathias, K Khair, C Burgess, et al.
Cell and Tissue Research|January 1, 1981
Pineal complex of the clawed toad, Xenopus laevis Daud.: structure and functionH W Korf, R Liesner, H Meissl, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 20, 2009
Prophylaxis with prothrombin complex concentrate in four children with severe congenital factor X deficiencyL Bowles, K Baker, K Khair, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 13, 2000
Severe factor V deficiency and neonatal intracranial haemorrhage: a case reportN Salooja, P Martin, K Khair, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
Intranasal desmopressin (Octim): a safe and efficacious treatment option for children with bleeding disordersK Khair, K Baker, M Mathias, et al.
British Journal of Haematology|March 1, 2008
ADAMTS 13 in non-thrombotic thrombocytopaenic purpura conditionsM Scully, R Liesner, C Burgess, et al.
British Journal of Haematology|November 14, 1997
Complications experienced with central venous catheters in children with congenital bleeding disordersP W Collins, K S Khair, R Liesner, et al.
Developmental Medicine and Child Neurology|April 20, 2001
Homozygous thermolabile variant of the methylenetetrahydrofolate reductase gene: a potential risk factor for hyperhomocysteinaemia, CVD, and stroke in childhoodM Prengler, N Sturt, S Krywawych, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 1, 2018
Prophylactic treatment of bleeding episodes in children <12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high-purity plasma-derived factor X (pdFX) concentrateR Liesner, C Akanezi, M Norton, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 1, 2000
The use of recombinant factor VIIa in a patient with severe Glanzmann's thrombasthenia to facilitate insertion of a Port-a-CathP Ancliff, R Liesner, K Khair, et al.
Pediatric Hematology and Oncology|November 24, 2004
Subcutaneous administration of protein C concentrateM Mathias, K Khair, C Burgess, et al.
Cell and Tissue Research|January 1, 1981
Pineal complex of the clawed toad, Xenopus laevis Daud.: structure and functionH W Korf, R Liesner, H Meissl, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 20, 2009
Prophylaxis with prothrombin complex concentrate in four children with severe congenital factor X deficiencyL Bowles, K Baker, K Khair, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 13, 2000
Severe factor V deficiency and neonatal intracranial haemorrhage: a case reportN Salooja, P Martin, K Khair, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
Intranasal desmopressin (Octim): a safe and efficacious treatment option for children with bleeding disordersK Khair, K Baker, M Mathias, et al.
British Journal of Haematology|March 1, 2008
ADAMTS 13 in non-thrombotic thrombocytopaenic purpura conditionsM Scully, R Liesner, C Burgess, et al.
British Journal of Haematology|November 14, 1997
Complications experienced with central venous catheters in children with congenital bleeding disordersP W Collins, K S Khair, R Liesner, et al.
Developmental Medicine and Child Neurology|April 20, 2001
Homozygous thermolabile variant of the methylenetetrahydrofolate reductase gene: a potential risk factor for hyperhomocysteinaemia, CVD, and stroke in childhoodM Prengler, N Sturt, S Krywawych, et al.
Pageof 7