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Results 1-10 of 27 (Search time: 0.007 seconds).
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Issue DateTitleAuthor(s)
2003The clinical effects of excessive a globin genes : two family studiesPremawardhena, A.P.; Fisher, C.A.; Rugless, M.; de Silva, S.; Perera, A.W.V.S.; Olivien, N.F.; Weatherall, D.J.
2007Cardiac functions in older patients with haemoglobin E- β thalassaemiaPremawardhena, A.P.; Wanninayake, S.; Dolapihilla, S.N.; Kapuruge, L.; Katugaha, N.; Olivieri, N.F.; Weatherall, D.J.
2010Parental awareness and cascade screening of thalassaemiaNishad, A.A.N.; Premawardhena, A.P.
2004Response of jaundice to phenobarbitone in thalassaemic patients co-inheriting Gilbert syndromePremawardhena, A.P.; Arambepola, M.; Fisher, C.A.; Oliveiri, N.F.; Weatherall, D.J.
2011The "Thal-index" with the BTT prediction, exe to discriminate Beta thalassaemia traits from other microcytic anaemiasNishad, A.A.N.; Wickremasinghe, A.R.; Pathmeswaran, A.; Premawardhena, A.P.
2010Liver dysfunction and its outcome in patients with dengue infectionKumarasena, R.S.; de Silva, A.P.; Keragala, B.S.D.P.; Premaratna, B.A.H.R.; Premawardhena, A.P.; Jayamanna, S.F.; de Silva, H.J.; de Silva, S.T.
2014Micro mapping of common alpha thalassaemia deletions (3.7 kb, 4.2 kb) in Sri Lanka and assessment of the contribution of alpha thalassemia to hypochromic microcytosisRodriao, B.K.R.P.; Perera, H.L.; Branava, U.; Manamperi, A.A.P.S.; Weatherall, D.J.; Premawardhena, A.P.
2003The worldwide prevalence of the UGT-1A1 promoter polymorphism as a contributor for phenotypic variability in thalassaemiaPremawardhena, A.P.; Lilt, Y.T.; Fisher, C.A.; Clegg, J.B.; Weatherall, D.J.
2011Do thalassaemic patients, their parents and caregivers support termination of pregnancy as a method for thalassaemia prevention?Nandasiri, A.S.D.; Dissakaruna, A.M.D.D.; Silva, D.P.S.I.; Nishad, A.A.N.; Premawardhena, A.P.
2013Role of red cell distribution width in screening for Hb E trait in population screening for haemoglobin disordersNishad, A.A.N.; de Silva, I.S.; Perera, H.L.; Pathmeswaran, A.; Premawardhena, A.P.