Dr David Rabbolini
1) The Sydney Platelet Group - co-ordinator
- A collaborative project assessing an integrated appraoch to the diagnosis of inherited platelet disorders.
2) Platelet Function Testing using OPTIMUL in patients with undiagnosed bleeding disorders in regional centres in Australia.
3) Treatment of itp: a multi-centre retrospective review.
2018TheEberhard F. Mammen Young Investigator Award
For the "Best presentation or meeting abstract by a young investigator — as presented or delivered to an international or large regional meeting on a topicrelated to the fields of thrombosis and hemostasis and whose subject matter is determined to be in the spirit of Dr. Mammen." (Dr Mammen was the Founding Editor of'Seminars in Thrombosis &Hemostasis' (STH))
2018The Peter Bancroft Prize,University of Sydney School of Medicine post-graduate prize
This is awarded to aDoctor of Philosophy graduate in Sydney Medical School whose thesis has been passed by all three examiners without requiring any emendation or amendmentsASTH Conference Grant Recipient,Awarded to the author of the best abstract in the bleeding disorders field submitted to either HAA or the ASTH scientific workshop.
2016ASTH Scientific Medal – Runner up.
2015ASTH Scientific Medal - Winner, Awarded for the best presentation at the annual scientific meeting, Adelaide, SA, 2015.
- The award is intended forindividuals working in clinical and laboratory research in the field of thrombosis and haemostasis.
- The award is judged on the basis of abstracts submitted to the annual combined meeting of the ASTH and the Haematology Society of Australia and New Zealand (HSANZ) and Australian and New Zealand Society of Blood Transfusion (ANZSBT).
2015 Abstract selected as one of theOutstanding young scientist abstracts from the Asia - Pacific region.
-Presented as an oral presentation at theAsia-Pacific society of Thrombosis and Haemostasis (APSTH)/ Japanese Society of Thrombosis and Haemostasis (JSTH) joint symposium in May 2015
Publications
Book Chapters
- Rabbolini, D., Morel-Kopp, M., Gabrielli, S., Chen, Q., Stevenson, W., Ward, C. (2015). DNA-based Diagnosis of Uncharacterized Inherited Macrothrombocytopenias Using Next-generation Sequencing Technology with a Candidate Gene Array. In Jerzy K Kulski (Eds.), Next Generation Sequencing: Advances, Applications and Challenges, (pp. 387-408). Rijeka, Croatia: InTech Publishers. [More Information]
Journals
- Scheim, D., Parry, P., Rabbolini, D., Aldous, C., Yagisawa, M., Clancy, R., Borody, T., Hoy, W. (2024). Back to the Basics of SARS-CoV-2 Biochemistry: Microvascular Occlusive Glycan Bindings Govern Its Morbidities and Inform Therapeutic Responses. Viruses, 16(4). [More Information]
- Coupland, L., Pai, K., Pye, S., Butorac, M., Miller, J., Crispin, P., Rabbolini, D., Stewart, A., Aneman, A. (2024). Protracted fibrinolysis resistance following cardiac surgery with cardiopulmonary bypass: A prospective observational study of clinical associations and patient outcomes. Acta Anaesthesiologica Scandinavica, 68(6), 772-780. [More Information]
- Coupland, L., Rabbolini, D., Schoenecker, J., Crispin, P., Miller, J., Ghent, T., Medcalf, R., Aneman, A. (2023). Point-of-care diagnosis and monitoring of fibrinolysis resistance in the critically ill: results from a feasibility study. Critical Care, 27(1). [More Information]
2024
- Scheim, D., Parry, P., Rabbolini, D., Aldous, C., Yagisawa, M., Clancy, R., Borody, T., Hoy, W. (2024). Back to the Basics of SARS-CoV-2 Biochemistry: Microvascular Occlusive Glycan Bindings Govern Its Morbidities and Inform Therapeutic Responses. Viruses, 16(4). [More Information]
- Coupland, L., Pai, K., Pye, S., Butorac, M., Miller, J., Crispin, P., Rabbolini, D., Stewart, A., Aneman, A. (2024). Protracted fibrinolysis resistance following cardiac surgery with cardiopulmonary bypass: A prospective observational study of clinical associations and patient outcomes. Acta Anaesthesiologica Scandinavica, 68(6), 772-780. [More Information]
2023
- Coupland, L., Rabbolini, D., Schoenecker, J., Crispin, P., Miller, J., Ghent, T., Medcalf, R., Aneman, A. (2023). Point-of-care diagnosis and monitoring of fibrinolysis resistance in the critically ill: results from a feasibility study. Critical Care, 27(1). [More Information]
2022
- Hsu, H., Chan, M., Armstrong, P., Crescente, M., Donikian, D., Kondo, M., Brighton, T., Chen, V., Chen, Q., Connor, D., Morel-Kopp, M., Stevenson, W., Ward, C., Rabbolini, D., et al (2022). A pilot study assessing the implementation of 96-well plate-based aggregometry (Optimul) in Australia. Pathology, 54(6), 746-754. [More Information]
- Rabbolini, D., Liang, H., Morel-Kopp, M., Connor, D., Whittaker, S., Dunkley, S., Donikian, D., Kondo, M., Chen, W., Stevenson, W., Campbell, H., Ward, C., Chen, V., et al (2022). Building platelet phenotypes: diaphanous-related formin 1 (DIAPH1)-related disorder. Platelets, 33(3), 432-442. [More Information]
- Connor, D., Rabbolini, D., Morel-Kopp, M., Fixter, K., Donikian, D., Kondo, M., Chan, O., Jarvis, S., Chen, W., Brighton, T., Chen, V., Ward, C., et al (2022). The utility of flow cytometric platelet forward scatter as an alternative to mean platelet volume. Platelets, 33(8), 1139-1145. [More Information]
2021
- Mason, G., Rabbolini, D. (2021). The Current Role of Platelet Function Testing in Clinical Practice. Seminars in Thrombosis and Hemostasis, 47(7), 843-854. [More Information]
2020
- Rabbolini, D., Connor, D., Morel-Kopp, M., Donikian, D., Kondo, M., Chen, W., Alessi, M., Stevenson, W., Chen, V., Joseph, J., Ward, C., et al (2020). An integrated approach to inherited platelet disorders: results from a research collaborative, the Sydney Platelet Group. Pathology, 52(2), 243-255. [More Information]
- Tang, C., Rabbolini, D., Morel-Kopp, M., Connor, D., Crispin, P., Ward, C. (2020). The clinical heterogeneity of RUNX1 associated familial platelet disorder with predisposition to myeloid malignancy - A case series and review of the literature. Research and Practice in Thrombosis and Haemostasis, 4(1), 106-110. [More Information]
2019
- Joseph, J., Rabbolini, D., Enjeti, A., Favaloro, E., Kopp, M., McRae, S., Pasalic, L., Tan, C., Ward, C., Chong, B. (2019). Diagnosis and management of heparin-induced thrombocytopenia: a consensus statement from the Thrombosis and Haemostasis Society of Australia and New Zealand HIT Writing Group. Medical Journal of Australia, 210(11), 509-516. [More Information]
- Rabbolini, D., Othman, M. (2019). Molecular and Genetic Testing in Thrombosis and Hemostasis. Seminars in Thrombosis and Hemostasis, 45(7), 657-660. [More Information]
2018
- Rabbolini, D., Chun, Y., Latimer, M., Kunishima, S., Fixter, K., Valecha, B., Tan, P., Chew, L., Kile, B., Burt, R., Gabrielli, S., Chen, Q., Stevenson, W., Ward, C., Morel-Kopp, M., et al (2018). Diagnosis and treatment of MYH9-RD in an Australasian cohort with thrombocytopenia. Platelets, 29(8), 793-800. [More Information]
- Fixter, K., Rabbolini, D., Valecha, B., Morel-Kopp, M., Gabrielli, S., Chen, Q., Stevenson, W., Ward, C. (2018). Mean platelet diameter measurements to classify inherited thrombocytopenias. International Journal of Laboratory Hematology, 40(2), 187-195. [More Information]
- Mundell, S., Rabbolini, D., Gabrielli, S., Chen, Q., Aungraheeta, R., Hutchinson, J., Kilo, T., Mackay, J., Ward, C., Stevenson, W., Morel-Kopp, M. (2018). Receptor homodimerization plays a critical role in a novel dominant negative P2RY12 variant identified in a family with severe bleeding. Journal of Thrombosis and Haemostasis, 16(1), 44-53. [More Information]
2017
- Rabbolini, D., Gardiner, E., Morel-Kopp, M., Dunkley, S., Jahangiri, A., Lee, C., Stevenson, W., Ward, C. (2017). Anti-glycoprotein VI mediated immune thrombocytopenia: An under-recognized and significant entity? Research and Practice in Thrombosis and Haemostasis, 1(2), 291-295. [More Information]
- Rabbolini, D., Morel-Kopp, M., Ward, C., Stevenson, W. (2017). GFI1B variants associated with thrombocytopenia. Platelets, 28(5), 525-527. [More Information]
- Rabbolini, D., Morel-Kopp, M., Chen, Q., Gabrielli, S., Dunlop, L., Chew, L., Blair, N., Brighton, T., Singh, N., Ng, A., Ward, C., Stevenson, W. (2017). Thrombocytopenia and CD34 expression is decoupled from (alpha)-granule deficiency with mutation of the first growth factor-independent 1B zinc finger. Journal of Thrombosis and Haemostasis, 15(11), 2245-2258. [More Information]
2015
- Rabbolini, D., Morel-Kopp, M., Gabrielli, S., Chen, Q., Stevenson, W., Ward, C. (2015). DNA-based Diagnosis of Uncharacterized Inherited Macrothrombocytopenias Using Next-generation Sequencing Technology with a Candidate Gene Array. In Jerzy K Kulski (Eds.), Next Generation Sequencing: Advances, Applications and Challenges, (pp. 387-408). Rijeka, Croatia: InTech Publishers. [More Information]
- Stevenson, W., Rabbolini, D., Beutler, L., Chen, Q., Gabrielli, S., Mackay, J., Brighton, T., Ward, C., Morel-Kopp, M. (2015). Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1. Blood, 126(17), 2027-2030. [More Information]
2014
- Rabbolini, D., Morel-Kopp, M., Stevenson, W., Ward, C. (2014). Inherited Macrothrombocytopenias. Seminars in Thrombosis and Hemostasis, 40(7), 774-784. [More Information]
Selected Grants
2019
- Platelet Function Testing using 96-well plate-based aggregometry OPTIMUL for Patients with Undiagnosed Bleeding Disorders in Regional Australia, Rabbolini D, Thrombosis & Haemostasis society of Australia and New Zealand Ltd/Science & Education Research Grant