Zobrazeno 1 - 10
of 90
pro vyhledávání: '"C. K. Kasper"'
Publikováno v:
Transfusion. 15:307-311
A three-year contract research program to study the production of cryoprecipitate has been completed. The investigators have collaborated to propose changes in the methods of production of cryoprecipitate. The investigators believe that the problem o
Publikováno v:
Transfusion. 15:312-322
Many aspects of the production of cryoprecipitate were studied to determine which methods resulted in the greatest recovery of Factor VIII. The following recommendations resulted: 1) blood should be mixed with anticoagulant throughout phlebotomy; 2)
Autor:
C. K. Kasper
Publikováno v:
Haemophilia. 8:166-169
Research subjects in developing countries may be especially vulnerable to exploitation. Scrupulous care should be taken to maintain the basic principles of ethical trial conduct: the right of participants to make their own informed decisions, a favor
Publikováno v:
Haemophilia. 7:537-543
A multicentre retrospective survey was conducted to assess the efficacy and side-effect profile of porcine factor VIII (pFVIII:C) given by continuous infusion (CI) to patients with congenital haemophilia A and inhibitors. Twenty-nine episodes in 18 p
Autor:
C. K. Kasper
Publikováno v:
Journal of Thrombosis and Haemostasis. 2:516-518
Autor:
C K Kasper, G Gjerset, R B Counts, J W Mosley, Mary Ann Fletcher, Elizabeth Donegan, M C Pike, Yi Zhou, J W Parker, J Hassett
Publikováno v:
Blood. 84:1666-1671
Low- and intermediate-purity clotting-factor therapies are believed to accelerate human immunodeficiency virus (HIV) progression in hemophiliacs through adverse immune effects of the other plasma proteins in the preparations. To investigate this post
Autor:
C. K. Kasper
Publikováno v:
Blood Coagulation & Fibrinolysis. 5:S63-S66
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 17
Autor:
C. K. Kasper, J.M. Lusher
Publikováno v:
Transfusion. 33:422-434
Autor:
C K, Kasper, J C, Lin
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(5)