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Australian and New Zealand Journal of Medicine|June 1, 1976
Assessment of the value of factor VIII procoagulant and antigen ratio in the diagnosis of carriers of haemophiliaS D'Souza, H Ekert, R Ananthakrishnan, et al.
Journal of Pediatric Surgery|June 1, 1983
The treatment of Wilms' tumor: results from Royal Children's Hospital, Melbourne, 1967-1977J M Hutson, M Kent, H Ekert, et al.
Blood|February 1, 1976
Platelet release abnormality associated with a variant of von Willebrand's diseaseS V Dowling, R H Muntz, S D'Souza, et al.
Australian Paediatric Journal|August 1, 1984
Experience with high dose multiagent chemotherapy and autologous bone marrow rescue in the treatment of twenty-two children with advanced tumoursH Ekert, K Tiedemann, K D Waters, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 31, 2001
Cost-utility analysis of recombinant factor VIIa (NovoSeven) in six children with long-standing inhibitors to factor VIII or IXH Ekert, T Brewin, W Boey, et al.
Thrombosis and Haemostasis|April 30, 1986
An inhibitor to factor VIII:C in a patient with possible combined haemophilia A and von Willebrand's diseaseL D Taylor, F L Dean, K Tiedemann, et al.
The Medical Journal of Australia|May 16, 1981
Results of cessation of treatment in childhood acute lymphocytic leukaemiaH Ekert, A Balderas, K D Waters, et al.
Medical and Pediatric Oncology|January 1, 1980
Prophylactic co-trimoxazole and lactobacilli preparation in neutropenic patientsH Ekert, I H Jurk, K D Waters, et al.
Blood|January 1, 1984
Left shift in the peripheral blood count at diagnosis in acute lymphocytic leukemia is significantly correlated with duration of complete remissionB J Shen, H Ekert, G P Tauro, et al.
Thrombosis Et Diathesis Haemorrhagica|November 15, 1975
Ristocetin in the diagnosis of von willebrand's disease: a comparison of rate and percent of aggregation with levels of the plasma factor(s) necessary for ristocetin aggregationS V Dowling, R H Muntz, S D'Souza, et al.
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