Treatment of aplastic anaemia with antil
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Nicolas Novitzky; Lucille Wood; Professor Peter Jacobs
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Article
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1991
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John Wiley and Sons
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English
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Twenty-three consecutive adults with bone marrow aplasia who, apart from one individual, lacked a sibling suitable for allogeneic transplantation, received five daily infusions of 50 mglkg of antilymphocyte globulin (ALG) concurrently with high-dose (500 mg) methylprednisolone (HDMP), followed by or