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  • Clinical and laboratory versus molecular markers for a correct classification of von Willebrand disease
  • Federici AB; Canciani MT
  • Haematologica 2009[May]; 94 (5): 610-5
  • von Willebrand disease (VWD) is the most common inherited bleeding disorder. In this perspective article, Drs. Federici and Canciani review how correlating the clinical, laboratory and genetic features of von Willebrand disease has led to improved understanding of its pathophysiology. They show how this has rationalized classification, which in turn can be used to improve treatment of these patients.
  • |*Mutation[MESH]
  • |Blood Platelets/metabolism[MESH]
  • |Electrophoresis, Agar Gel[MESH]
  • |Humans[MESH]
  • |Molecular Weight[MESH]
  • |Protein Multimerization[MESH]
  • |von Willebrand Diseases/classification/diagnosis/*genetics[MESH]
  • |von Willebrand Factor/chemistry/*genetics/metabolism[MESH]





  • *{{pmid19407316}}
    *<b>[http://www.kidney.de/mlpefetch.php?search=19407316 Clinical and laboratory versus molecular markers for a correct classification of von Willebrand disease ]</b> Haematologica 2009; 94(5) ; 610-5 Federici AB; Canciani MT

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    Haematologica

    610 5.94 2009