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Issue DateTitleAuthor(s)
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.
2021Screening of children with anaemia for iron deficiency and thalassaemia trait provides an opportunity for thalassaemia prevention in Sri LankaMettananda, S.
2021Genetic and epigenetic therapies for β-Thalassaemia by altering the expression of α-globin geneMettananda, S.
2021Acute on chronic osteomyelitis due to coliforms in a Sri Lankan child with homozygous sickle cell diseaseHoole, T.J.; Arunath, V.; de Silva, M.H.A.D.; Muthukumarana, O.G.W.; Kumarasiri, I.M.; Rathnasiri, G.B.A.M.R.; Mahendra, G.; Premawardhena, A.; Mettananda, S.
2021Multisystem inflammatory syndrome in children: A Sri Lankan case seriesSandakelum, U.; Samararathna, R.; Pathiraja, H.; de Silva, L.; Balasubramaniam, R.; de Abrew, G.; Adihetty, D.; Fernando, M.; Randeny, S.; Mettananda, S.
2021A child with Imerslund-Gräsbeck syndrome concealed by co-existing α-thalassaemia presenting with subacute combined degeneration of the spinal cord: a case reportArunath, V.; Hoole, T. J.; Rathnasri, A.; Muthukumarana, O.; Kumarasiri, I.M.; Liyanage, N.D.; Costa, Y.; Mettananda, S.
2021A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report.Rathnasiri, A.; Senarathne, U.; Arunath, V.; Hoole, T.; Kumarasiri, I.; Muthukumarana, O.; Jasinge, E.; Mettananda, S.
2021A Sri Lankan boy with Thurston syndrome (type V oro-facio-digital syndrome)Athapathu, A.S.; Aruppala, A.A.H.S.; Hoole, T.J.; Arunath, V.; Rathnasiri, G.B.A.M.; Mettananda, S.

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