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Issue Date	Title	Author(s)
2018	Smith-Lemli-Opitz syndrome presenting as acute adrenal crisis in a child: a case report	Jayamanne, C.; Sandamal, S.; Jayasundara, K.; Saranavananthan, M.; Mettananda, S.
2018	Chiari malformation type 1 presenting as unilateral progressive foot drop: a case report and review of literature	Jayamanne, C.; Fernando, L.; Mettananda, S.
2020	Recent developments in the treatment of transfusion dependent thalassaemia	Mettananda, S.
2020	Marriage patterns in Sri Lanka and the prevalence of parental consanguinity in patients with β-thalassaemia: a cross-sectional descriptive analysis	Premawardhena, A.P.; de Silva, S.T.; Goonatilleke, M.D.D.C.; Ediriweera, D.S.; Mettananda, S.; Rodrigo, B.K.R.P.; Allen, A.; Weatherall, D.J.
2019	Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report.	Uyangoda, K.; Kamalanathan, P.; Mettananda, S.
2020	Improving standards of care for children with thalassaemia in Sri Lanka	Mettananda, S.
2020	Severe disfiguring scalp and facial oedema due to Henoch–Schönlein Purpura in a child	Arunath, V.; Athapathu, A.S.; Hoole, T.J.; Aruppala, H.; Rathnasri, A.; Ranawaka, R.; Mettananda, S.
2020	Congenital intrahepatic Portosystemic shunt presenting with Muco-Cutaneous bleeding	Galappaththi, S.; Rajindrajith, S.; Mettananda, S.
2020	Patient perspectives on barriers to participating in cardiac rehabilitation	Mettananda, C.; Ismail, I.; Mettananda, S.
2021	Oxidative status in the β-thalassemia syndromes in Sri Lanka; a cross-sectional survey	Allen, 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.