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  1. Combined effects of two mutations in von Willebrand disease 2M phenotype
  2. Type 2B von Willebrand disease, diagnosis
  3. Identification of p.W246L As a Novel Mutation in the GP1BA Gene Responsible for Platelet-Type von Willebrand Disease
  4. von Willebrand disease in a single institution in Argentina, December 2017
  5. C0379 Several polymorphisms in the ADAMTS13 gene in a patient with thrombotic thrombocytopenic purpura (TTP)
  6. Major haemorrhage related to surgery in patients with type 1 and possible type 1 von Willebrand disease