Utility of the ISTH bleeding assessment tool in predicting platelet defects in participants with suspected inherited platelet function disorders

Gelijkaardige items

• Diagnostic utility of the ISTH bleeding assessment tool in patients with suspected platelet function disorders
  door: Adler, Marcel, et al.
  Gepubliceerd in: (2019)
• Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function
  door: Maclachlan, Annabel, et al.
  Gepubliceerd in: (2017)
• Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel
  door: Dawood, Ban B., et al.
  Gepubliceerd in: (2012)
• SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects
  door: Fletcher, Sarah J., et al.
  Gepubliceerd in: (2015)
• Menstrual and obstetrical bleeding in women with inherited platelet receptor defects—A systematic review
  door: Punt, Marieke C., et al.
  Gepubliceerd in: (2020)