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

Παρόμοια τεκμήρια

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