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Results 1-10 of 34 (Search time: 0.003 seconds).
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Issue DateTitleAuthor(s)
2012The Thal-index with the BTT prediction.exe to discriminate ß-thalassaemia traits from other microcytic anaemiasNishad, A.A.N.; Pathmeswaran, A.; Wickremasinghe, A.R.; Premawardhena, A.
2015Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia traitJones, E.; Pasricha, S.R.; Allen, A.; Evans, P.; Fisher, C.A.; Wray, K.; Premawardhena, A.; Bandara, D.; Perera, A.; Webster, C.; Sturges, P.; Olivieri, N.F.; St Pierre, T.; Armitage, A.E.; Porter, J.B.; Weatherall, D.J.; Drakesmith, H.
2019Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri LankaPerera, S.; Allen, A.; Silva, I.; Hapugoda, M.; Wickramarathne, M.N.; Wijesiriwardena, I.; Allen, S.; Rees, D.; Efremov, D.G.; Fisher, C.A.; Weatherall, D.J.; Premawardhena, A.
2020Sickle cell disease in Sri Lanka: clinical and molecular basis and the unanswered questions about disease severityDarshana, T.; Bandara, D.; Nawarathne, U.; de Silva, U.; Costa, Y.; Pushpakumara, K.; Pathirage, S.; Basnayake, S.; Epa, C.; Dilrukshi, P.; Wijayawardena, M.; Anthony, A. A.; Rodrigo, R.; Manamperi, A.; Smith, F.; Allen, A.; Menzel, S.; Rees, D.; Premawardhena, A.
2020Comparison of liver MRI R2(FerriScan®) VS liver MRI T2* as a measure of body iron load in a cohort of Beta Thalassaemia major patientsPadeniya, P.; Siriwardana, S.; Ediriweera, D.; Samarasinghe, N.; Silva, S.; Silva, I.; Ahamed, N.; Niriella, M.A.; Premawardhena, A.
2021Oxidative status in the β-thalassemia syndromes in Sri Lanka; a cross-sectional surveyAllen, A.; Perera, S.; Mettananda, S.; Rodrigo, R.; Perera, L.; Darshana, T.; Moggach, F.; Crawford, A.J.; Heirene, L.; Fisher, C.; Olivieri, N.; Rees, D.; Premawardhena, A.; Allen, S.
2021A Comprehensive review of hydroxyurea for β-haemoglobinopathies: the role revisited during COVID-19 pandemicYasara, N.; Premawardhena, A.; Mettananda, S.
2021Hydroxyurea and blood transfusion therapy for Sickle cell disease in South Asia: inconsistent treatment of a neglected diseaseDarshana, T.; Rees, D.; Premawardhena, A.
2018Anaemia among females in child-bearing age: Relative contributions, effects and interactions of α- and β-thalassaemia.Mettananda, S.; Suranjan, M.; Fernando, R.; Dias, T.; Mettananda, C.; Rodrigo, R.; Perera, L.; Gibbons, R.; Premawardhena, A.; Higgs, D.
2018Body iron status of children and adolescents with transfusion dependent β-thalassaemia: trends of serum ferritin and associations of optimal body iron controlSuriyapperuma, T.; Peiris, R.; Mettananda, C.; Premawardhena, A.; Mettananda, S.