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Interest in the treatment of hemophilia has increased greatly in recent years, largely due to the availability of concentrated preparations of antihemophilic globulin (factor VIII). Intensive replacement therapy of acute bleeding episodes can prevent many of the orthopedic disabilities classically associated with this disease and no doubt has improved the life expectancy of afflicted individuals. It is necessary, therefore, that all physicians become more aware of the optimal approach to the patient with hemophilia.
Dr. Strauss attempts to distill the very large experience of one major clinical center into a practical guide to therapy in this little manual. The result
Diagnosis and Treatment of Hemophilia.. Ann Intern Med. 1969;70:244. doi: https://doi.org/10.7326/0003-4819-70-1-244_1
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Published: Ann Intern Med. 1969;70(1):244.
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