Research publications

Journal articles

Ramanan R, Parikh S, Aung LL, McFadyen JD, Tran HA. Intraindividual bleeding outcomes in patients with hemophilia a on emicizumab prophylaxis in Australia. Blood Vessels, Thrombosis & Hemostasis. 2024;1:100005

Ramanan R, Evans N, Kaplan Z, McFadyen JD, Tran HA. Mutational landscape, inhibitor development, and health-care burden in non-severe haemophilia a: A single-centre Australian experience. Haemophilia. 2024

George C, Parikh S, Carter T, Morris A, Cramey C, McElroy K, Tran H. Haemophilia joint health score (HJHS) usage, patterns and outcome data in patients with haemophilia A and haemophilia B in Australia: A descriptive study using the Australian bleeding disorders registry (ABDR). Haemophilia. 2023;29:1135-1141

George C, Parikh S, Carter T, McCosker J, Carlino S, Tran H. Evaluation of treatment and outcome for patients with haemophilia A and haemophilia B on extended half-life (EHL) factor products: A 12-month data analysis. Haemophilia. 2023;29:1283-1290

Hunt S, Robertson J, Conn J, Casey J, Royle J, Collins J, Hourigan M, Richmond J, Yang Wang T, Mills A, Mason J. A low-dose rituximab regimen for first-line treatment of acquired haemophilia A. Eur J Haematol. 2022;108:28-33

Brown LJ, La HA, Li J, Brunner M, Snoke M, Kerr AM. The societal burden of haemophilia A. II - the cost of moderate and severe haemophilia A in Australia. Haemophilia. 2020;26 Suppl 5:11-20

Brennan Y, Parikh S, McRae S, Tran H. The Australian experience with switching to extended half-life factor VIII and IX concentrates: On behalf of the Australian Haemophilia Centre Directors' Organisation. Haemophilia. 2020;26:529-535

Mason JA, Parikh S, Tran H, Rowell J, McRae S. Australian multicentre study of current real-world prophylaxis practice in severe and moderate haemophilia A and B. Haemophilia. 2018;24:253-260

Conference abstracts

Ramanan R, P'Ng S, Goruppi M, McFadyen JD, Tran H. Evaluation of real-world peri-operative outcomes in patients with haemophilia a (ha) with or without inhibitors on emicizumab prophylaxis in Australia. Blood 2022 and ISTH 2024

Ramanan R, P'Ng S, Goruppi M, Curnow J, Hooi A, Perkins AC, McFadyen JD, Tran HA. Phenotypic characterisation of congenital fibrinogen disorders in Australia. ISTH. 2024

Ramanan R, Parikh S, McFadyen JD, Tran H. Evaluation of real-world bleeding outcomes in patients with haemophilia A (HA) with or without inhibitors on emicizumab prophylaxis in Australia. ISTH. 2023

Ramanan R, Parikh S, McFadyen JD, Tran H. Phenotypic characterisation of congenital fibrinogen disorders: A single centre experience. Blood. 2022

Ramanan R, Parikh S, McFadyen JD, Tran H. Evaluation of real-world bleeding outcomes in patients with haemophilia A (HA) with or without inhibitors on emicizumab prophylaxis in Australia. Monash University Translational Symposium and Blood. 2022

Parikh S, George C, McRae S, Carter T, McCosker J, Carlino S, Tran H. Comprehensive evaluation of treatment and outcome forpatients with haemophilia a and haemophilia b on extended half life (EHL) products: A 12 month data analysis. Blood. 2021

Brennan Y. The basics about blood clotting and how this interacts with factor replacement/novel therapies. 19th Australian Conference on haemophilia, VWD & rare bleeding disorders. 2019

Brennan Y, Hooi A, Shoemark R, Curtin JA. SMS bleed capture project. Blood. 2019

Brennan Y, Kershaw G, Cai N, Curtin JA. Investigation of a prolonged aptt reveals a rare finding. Blood. 2019

Brennan Y, Parikh S, McRae S, Tran H. Extended half-life clotting factor use in Australia. Blood. 2019

Campbell S, Ekert JE, Furmedge JF, Barnes CD. Haemostatic therapy for the insertion of central venous access devices in severe haemophilia a and b - Melbourne paediatric protocol. ISTH. 2019

Campbell S, Parikh S, Tran H. Genetic landscape of haemophilia A and B in Australia. ISTH. 2019

Mason J, Parikh S, McRae S, Barnes CD. Impact of the sippet study on management of Australian pups. International Society on Thrombosis and Haemostasis (ISTH). 2019

Tiao J. Alternative splicing as a future treatment for haemophilia A. Blood. 2019

Tiao J, Powell S, Gilmore G, Veedu R, Wilton S, Baker RI. Targeted exon skipping as a potential gene correction therapy for haemophilia. ISTH. 2019

Tiao J. Gene skipping of factor VIII gene transcript as a future treatment for haemophilia A. 10th Congress of APSTH. 2018

Mason J, Parikh S. In pursuit of pristine joints: Where are we with prophylaxis? 18th Australian & New Zealand Conference on Haemophilia & Rare Bleeding Disorders. 2017

Menezes M, Wilton S, Veedu R, Hughes QW, Baker RI. Altering the splicing of the F8 mRNA transcript as a future treatment for haemophilia. HAA Annual Scientific Meeting. 2017

McRae S, Parikh S, Tran H. Characterisation of the inhibitor status of patients with haemophilia a in Australia. ISTH. 2017

Tran H. Exploring the possible effects of tranexamic acid administration on the immune and inflammatory responses in patients with haemophilia. ISTH. 2017

McCosker J. Remote control – patient and clinician satisfaction of using telehealth. World Federation of Haemophilia Congress. 2016

Rowell J, Caris S, Gunn S, Simon G, Barnes C. Australian Bleeding Disorders Registry (ABDR) – an update. World Federation of Hemophilia World Congress. 2012