Use of DDAVP in inherited and acquired platelet dysfunction
Author:
Publisher
Wiley
Subject
Hematology
Reference25 articles.
1. 1-DEAMINO-8-D-ARGININE VASOPRESSIN: A NEW PHARMACOLOGICAL APPROACH TO THE MANAGEMENT OF HAEMOPHILIA AND VON WILLEBRAND'S DISEASE
2. Response of Factor VIII/von Willebrand Factor to DDAVP in Healthy Subjects and Patients with Haemophilia A and von Willebrand's Disease
3. The Release of Plasminogen Activator and Factor VIII after Injection of DDAVP in Healthy Volunteers and in Patients with von Willebrand's Disease
4. DDAVP: A useful alternative to blood components in moderate hemophilia A and von Willebrand disease
5. Deamino-8-D-Arginine Vasopressin Shortens the Bleeding Time in Uremia
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