Browsing by Author Premawardhena, A.

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Issue DateTitleAuthor(s)
2019The p.H63D allele of the HFE gene protects against low iron stores in Sri Lanka.Allen, A.; Premawardhena, A.; Allen, S.; Rodrigo, R.; Manamperi, A.; Perera, L.; Wray, K.; Armitage, A.; Fisher, C.; Drakesmith, A.; Robson, K.; Weatherall, D.
2021Pitfalls in the diagnosis of β-Thalassemia IntermediaPerera, S.; Allen, A.; Rees, DC.; Premawardhena, A.
2019Place for elective cholecystectomy for patients with severe thalassaemia: a retrospective case control study.Premawardhena, A.; Fernando, R.; Kumarage, S.; Nishad, N.; Goonatilleke, D.; Silva, I.; Mettananda, S.
2018Possible Application of Sickling Test in Haemoglobinopathy Screening of Sri Lanka.Darshana, T.; Perera, N.; Manamperi, A.; Premawardhena, A.
2020Psychological morbidity among children with transfusion dependent β-thalassaemia and their parents in Sri LankaMettananda, S.; Peiris, R.; Pathiraja, H.; Chandradasa, M.; Bandara, D.; de Silva, U.; Mettananda, C.; Premawardhena, A.
2023Pyrexia of unknown origin (PUO) and the cost of care in a tertiary care institute in Sri LankaPremathilaka, R.; Darshana, T.; Ekanayake, C.; Chathurangani, K.C.; Mendis, I.; Perinparajah, S.; Shashiprabha, M.; Nishshanka, S.; Tilakaratna, Y.; Premawardhena, A.
2018Quality of life and psychological morbidity among children with transfusion dependent thalassaemia and their parentsMettananda, S.; Pathiraja, H.; Peiris, R.; Bandara, D.; de Silva, T.U.N.; Mettananda, K.C.D.; Premawardhena, A.
2022A randomised double-blind placebo-controlled clinical trial of oral hydroxyurea for transfusion-dependent β-thalassaemiaYasara, N.; Wickramarathne, N.; Mettananda, C.; Silva, I.; Hameed, N.; Attanayaka, K.; Rodrigo, R.; Wickramasinghe, N.; Perera, L.; Manamperi, A.; Premawardhena, A.; Mettananda, S.
2015Rare hemoglobin variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB:c.206T>C) in Sri Lankan familiesPerera, P.S.; Silva, I.; Hapugoda, M.; Wickramarathne, M.N.; Wijesiriwardena, I.; Efremov, D.G.; Fisher, C.A.; Weatherall, D.J.; Premawardhena, A.
2005Reappraisal of symptoms and signs of uncomplicated β thalassemia traitPremawardhena, A.; Malewana, T.; Weerasinghe, M.; Arambepola, M.
2022Redesigning new policy options for thalassemia prevention in Sri LankaAmarasinghe, N.; Amarasena, A.; Thabrew, A.; Werawatte, P.; Premawardhena, A.; Malik, F.; Abusayeed, M.; Wickramasinghe, C.
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.
1997Stroke subtypes in Sri LankaGunatilake, S.B.; Premawardhena, A.
2008Studies in haemoglobin E beta-thalassaemiaOlivieri, N. F.; Muraca, G. M.; O Donnell, A.; Premawardhena, A.; Fisher, C.; Weatherall, D. J.
2022A Systematic review on diagnostic methods of red cell membrane disorders in AsiaSilva, R.; Amarasinghe, D.; Perera, S.; Premawardhena, A.
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.
2024Unresolved laboratory issues of the heterozygous state of β-thalassemia: a literature reviewThilakarathne, S.; Jayaweera, U.P.; Premawardhena, A.
2022Using FIB-4 score as a screening tool in the assessment of significant liver fibrosis (F2) in patients with transfusion-dependent beta thalassaemia: a cross-sectional studyPadeniya, P.; Ediriweera, D.S.; de Silva, A.P.; Niriella, M.A.; Premawardhena, A.
2005Using red cell indices as a screening test for the detection of haemoglobin E trait in population screening for haemoglobin disordersPremawardhena, A.; Samarakoon, S.; Perera, U.; Samaranayake, R.; Arambepola, M.
2006The variable phenotypes of haemoglobin D in Sri Lankan patientsPremawardhena, A.; Arambepola, M.; Weatherall, D.