Hasil Pencarian - Visvalingam Arunath
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A Sri Lankan child with hypersplenism secondary to pre-hepatic portal hypertension, successfully managed with partial splenic artery embolization: a case report and review of the l... oleh Visvalingam Arunath, Manoj Sanjeewa Liyanarachchi, Sundarraajah Gajealan, Kumudu Weerasekara
Diterbitkan 2022-07-01
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A novel mutation in ACADVL causing very long-chain acyl-coenzyme-A dehydrogenase deficiency in a South Asian pediatric patient: a case report and review of the literature oleh Visvalingam Arunath, Manoj Sanjeewa Liyanarachchi, Sundararajah Gajealan, Eresha Jasinge, Kumudu Weerasekara, Lia Abbasi Moheb
Diterbitkan 2021-09-01
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A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report oleh Asanka Rathnasiri, Udara Senarathne, Visvalingam Arunath, Thabitha Hoole, Ishara Kumarasiri, Oshanie Muthukumarana, Eresha Jasinge, Sachith Mettananda
Diterbitkan 2021-10-01
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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 oleh Visvalingam Arunath, Thabitha Jebaseeli Hoole, Asanka Rathnasri, Oshanie Muthukumarana, Ishara Minuri Kumarasiri, Nishadi Dananjani Liyanage, Yasintha Costa, Sachith Mettananda
Diterbitkan 2021-01-01
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