Browsing by Author Arunath, V.

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Showing results 1 to 7 of 7
Issue DateTitleAuthor(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.
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.
2020Delayed-onset Sinus Node Dysfunction in a child victim of Russell's Viper Bite.Athapathu, A.S.; Arunath, V.; Aruppala, A.A.; Hoole, T. J.; Suntharesan, K.; Mettananda, S.
2016Knowledge, attitudes and practices related to chronic childhood urinary tract infections among care givers of patients with urinary tract infections - a single centre experienceArunath, V.; Gnanasekar, B.; Coonghe, P.A.D.; Sathiadas, M.G.
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.
2020Severe disfiguring scalp and facial oedema due to Henoch–Schönlein Purpura in a childArunath, V.; Athapathu, A.S.; Hoole, T.J.; Aruppala, H.; Rathnasri, A.; Ranawaka, R.; 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.