The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort studyPaula D. James, David Lillicrap, Christine Brown et al.|Blood|2006Cited by 351
Founder von Willebrand factor haplotype associated with type 1 von Willebrand diseaseLee A. O’Brien, David Lillicrap, Paula D. James et al.|Blood|2003Cited by 97
Measurement of Bradykinin Formation and Degradation in Blood Plasma: Relevance for Acquired Angioedema Associated With Angiotensin Converting Enzyme Inhibition and for Hereditary Angioedema Due to Factor XII or Plasminogen Gene VariantsFrançois Marceau, Konrad Bork, Georges E. Rivard et al.|Frontiers in Medicine|2020Cited by 33