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Results 1-10 of 14 (Search time: 0.003 seconds).
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Issue DateTitleAuthor(s)
201920 year follow up and survival analysis in a cohort of patients with Haemoglobin E beta Thalassaemia.Olivieri, N.F.; Premawardhena, A.P.; Amir-Arsalan, S.; Ediriweera, D.; Mettananda, S.; Bandara, W.D.; Arambepola, M.; de Silva, S.; Refai, M.A.C.M.; Allen, A.
2019A child with Gradenigo syndrome presenting with meningism: a case report.Athapathu, A. S.; Bandara, E. R. S.; Aruppala, A. A. H. S.; Chandrapala, K. M. A. U.; Mettananda, S.
2019Identifying haemoglobinopathy traits and iron deficiency in Sri Lanka using the dtchlorophenolindophenol (DCIP) and one- tube osmotic fragility (OF) tests and measurement of red cell zinc protoporphyrin (ZPP)Perera, P. S.; Premawardhena, A.; Mettananda, S.; Rodrigo, R.; Perera, L.; Weatherall, D. J.; Allen, S.; Allen, A.
2019Analysis of nutritional status and factors associated with undernutrition in children aged 6-59 months in a rural area of Sri LankaSamarasekara, G.S.; Mettananda, S.; Punchihewa, P.
2019Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report.Uyangoda, K.; Kamalanathan, P.; Mettananda, S.
2019Marriage patterns in Sri Lanka and the role of consanguinity in thalassaemia: A cross sectional descriptive analysisGoonatilleke, M.D.D.C.; de Silva, S.T.; Rodrigo, R.; Perera, S.; Goonathilaka, G.W.M.R.G.B.; Ramees, L.; Mettananda, S.; Weatherall, D.L.; Premawardhena, A.P.
2019Blood transfusion therapy for β-thalassemia major and hemoglobin E β-thalassemia: adequacy, trends, and determinants in Sri Lanka.Mettananda, S.; Pathiraja, H.; Peiris, R.; Wickramarathne, N.; Bandara, D.; de Silva, U.; Mettananda, C.; Premawardhena, A.
2019Health related quality of life among children with transfusion dependent β-thalassaemia major and haemoglobin E β-thalassaemia in Sri Lanka: a case control study.Mettananda, S.; Pathiraja, H.; Peiris, R.; Bandara, D.; de Silva, U.; Mettananda, C.; Premawardhena, A.
2019Synergistic silencing of α-globin and induction of γ-globin by histone deacetylase inhibitor, vorinostat as a potential therapy for β-thalassaemiaMettananda, S.; Yasara, N.; Fisher, C. A.; Taylor, S.; Gibbons, R.; Higgs, D.
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.