David J. Rabbolini

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

William Stevenson, David J. Rabbolini, Lucinda Beutler et al. · Blood · 2015 · 75 citations

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

David J. Rabbolini, Marie‐Christine Morel‐Kopp, Qihua Chen et al. · Journal of Thrombosis and Haemostasis · 2017 · 28 citations · Full text

Thrombopoiesis, Autoimmune Disease, α‐Granule Deficiency +10

Diagnosis and management of heparin‐induced thrombocytopenia: a consensus statement from the Thrombosis and Haemostasis Society of Australia and New Zealand<scp>HIT</scp>Writing Group

Joanne Joseph, David J. Rabbolini, Anoop Enjeti et al. · The Medical Journal of Australia · 2019 · 28 citations

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

Stuart J. Mundell, David J. Rabbolini, Sara Gabrielli et al. · Journal of Thrombosis and Haemostasis · 2017 · 25 citations · Full text

Receptor Homodimerization, Critical Role, Immunology +3

Mean platelet diameter measurements to classify inherited thrombocytopenias

Kate Fixter, David J. Rabbolini, Bhavia Valecha et al. · International Journal of Laboratory Hematology · 2017 · 25 citations