All Stories

  1. Receptor homodimerization plays a critical role in a novel dominant negative P2RY12 variant identified in a family with severe bleeding

    Article • Journal of Thrombosis and Haemostasis, December 2017, Wiley

    david rabbolini, Marie-Christine Morel-Kopp

  2. Mean platelet diameter measurements to classify inherited thrombocytopenias

    Article • International Journal of Laboratory Hematology, November 2017, Wiley

    david rabbolini, Marie-Christine Morel-Kopp

  3. Diagnosis and treatment of MYH9-RD in an Australasian cohort with thrombocytopenia

    Article • Platelets, November 2017, Taylor & Francis

    david rabbolini, Dr robert j bird, Marie-Christine Morel-Kopp, WALTER CHEN

  4. Thrombocytopenia and CD34 expression is decoupled from α-granule deficiency with mutation of the first growth factor-independent 1B zinc finger

    Article • Journal of Thrombosis and Haemostasis, October 2017, Wiley

    david rabbolini, Marie-Christine Morel-Kopp

  5. Anti-glycoprotein VI mediated immune thrombocytopenia: An under-recognized and significant entity?

    Article • Research and Practice in Thrombosis and Haemostasis, August 2017, Wiley

    david rabbolini, Marie-Christine Morel-Kopp

  6. GFI1B variants associated with thrombocytopenia

    Article • Platelets, June 2017, Taylor & Francis

    david rabbolini, Marie-Christine Morel-Kopp

  7. Mean platelet diameter measurements to classify inherited thrombocytopenias

    Article • Pathology, February 2017, Elsevier

    david rabbolini

  8. In situ diagnostic methods for catheter related bloodstream infection in burns patients: A pilot study

    Article • Burns, March 2016, Elsevier

    david rabbolini

  9. ‘Epinephrine-resistant’ angioedema

    Article • BMJ Case Reports, January 2016, BMJ

    david rabbolini

  10. DNA-based Diagnosis of Uncharacterized Inherited Macrothrombocytopenias Using Next-generation Sequencing Technology with a Candidate Gene Array

    Article • January 2016, IntechOpen

    david rabbolini

  11. Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1

    Article • Blood, August 2015, American Society of Hematology

    david rabbolini, Marie-Christine Morel-Kopp

  12. Next generation sequencing using a candidate gene array for the diagnosis of uncharacterised inherited macrothrombocytopenias

    Article • Pathology, January 2015, Elsevier

    david rabbolini

  13. Inherited Macrothrombocytopenias

    Article • Seminars in Thrombosis and Hemostasis, August 2014, Thieme Publishing Group

    david rabbolini, Marie-Christine Morel-Kopp

  14. Multiple squamous cell carcinomas following introduction of nilotinib

    Article • Clinical and Experimental Dermatology, August 2014, Wiley

    david rabbolini

  15. Systemic capillary leak syndrome: recognition prevents morbidity and mortality

    Article • Internal Medicine Journal, October 2013, Wiley

    david rabbolini