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Showing 3 out of a total of 3 results for community: Medicine.
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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
)
Acute disseminated encephalomyelitis presenting as bilateral ptosis in a Sri Lankan Child
Kumarasiri, I.
;
Samararathna, R.
;
Sandakelum, U.
;
Muthukumarana, O.
;
Balasubramaniam, R.
;
Mettananda, S.
(
Hindawi Pub. Corp.
,
2022
)
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Author
Mettananda, S. (3)
Muthukumarana, O. (3)
Arunath, V. (2)
Kumarasiri, I. (2)
Balasubramaniam, R. (1)
Costa, Y. (1)
Hoole, T. (1)
Hoole, T. J. (1)
Jasinge, E. (1)
Kumarasiri, I.M. (1)
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Subject
Child (1)
Congenital adrenal hypoplasia (1)
Encephalomyelitis (1)
thalassaemia (1)
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Date Issued
2021 (2)
2022 (1)
Has File(s)
Yes (3)