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Showing 10 out of a total of 62 results for collection: Journal/Magazine Articles.
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Place 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.
(
BioMed Central,London
,
2019
)
Screening of children with anaemia for iron deficiency and thalassaemia trait provides an opportunity for thalassaemia prevention in Sri Lanka
Mettananda, S.
(
Sri Lanka College of Paediatricians
,
2021
)
Efficacy and safety of oral hydroxyurea in transfusion-dependent β-thalassaemia: a protocol for randomised double-blind controlled clinical trial
Yasara, N.
;
Wickramarathne, N.
;
Mettananda, C.
;
Manamperi, A.
;
Premawardhena, A.
;
Mettananda, S.
(
BMJ Publishing Group Ltd.
,
2020
)
Spondylocostal Dysplasia in a 7-year-old Sri Lankan girl causing restrictive lung disease: A case report and review of the literature
Kamalanathan, P.
;
Fernando, M.
;
Jayawardena, R.
;
Upasena, A.
;
Rajindrajith, S.
;
Mettananda, S.
(
Hindawi Pub. Corp.
,
2020
)
Genetic and epigenetic therapies for β-Thalassaemia by altering the expression of α-globin gene
Mettananda, S.
(
Frontiers Media S.A
,
2021
)
Acute on chronic osteomyelitis due to coliforms in a Sri Lankan child with homozygous sickle cell disease
Hoole, 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.
(
Sri Lanka College of Paediatricians
,
2021
)
Multisystem inflammatory syndrome in children: A Sri Lankan case series
Sandakelum, U.
;
Samararathna, R.
;
Pathiraja, H.
;
de Silva, L.
;
Balasubramaniam, R.
;
de Abrew, G.
;
Adihetty, D.
;
Fernando, M.
;
Randeny, S.
;
Mettananda, S.
(
Sri Lanka College of Paediatricians
,
2021
)
A child with Imerslund-Gräsbeck syndrome concealed by co-existing α-thalassaemia presenting with subacute combined degeneration of the spinal cord: a case report
Arunath, V.
;
Hoole, T. J.
;
Rathnasri, A.
;
Muthukumarana, O.
;
Kumarasiri, I.M.
;
Liyanage, N.D.
;
Costa, Y.
;
Mettananda, S.
(
BioMed Central
,
2021
)
A 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.
(
BioMed Central,
,
2021
)
Psychological morbidity among children with transfusion dependent β-thalassaemia and their parents in Sri Lanka
Mettananda, S.
;
Peiris, R.
;
Pathiraja, H.
;
Chandradasa, M.
;
Bandara, D.
;
de Silva, U.
;
Mettananda, C.
;
Premawardhena, A.
(
Public Library of Science
,
2020
)
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Author
Mettananda, S. (62)
Premawardhena, A. (13)
Mettananda, C. (8)
Pathiraja, H. (8)
Arunath, V. (5)
de Silva, U. (5)
Peiris, R. (5)
Allen, A. (4)
Bandara, D. (4)
Samararathna, R. (4)
... View More
Subject
Thalassaemia (5)
Child (4)
thalassaemia (4)
Anaemia (3)
Sri Lanka (3)
Thalassemia (3)
thalassemia (3)
beta-Thalassemia (2)
Hydroxyurea (2)
Iron deficiency (2)
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Date Issued
2020 - 2024 (35)
2012 - 2019 (27)
Has File(s)
Yes (62)