Search Results - Eresha Jasinge

Cornea Verticillata in classical Fabry disease, first from Sri Lanka: a case report by Hasani Hewavitharana, Eresha Jasinge, Hiranya Abeysekera, Jithangi Wanigasinghe

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A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia by Dinesha Maduri Vidanapathirana, Subashinie Jayasena, Eresha Jasinge, Blanka Stiburkova

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Evaluation of biochemical and haematological changes in dengue fever and dengue hemorrhagic fever in Sri Lankan children: a prospective follow up study by Grace Angeline Malarnangai Kularatnam, Eresha Jasinge, Sunethra Gunasena, Dulani Samaranayake, Manouri Prasanta Senanayake, Vithanage Pujitha Wickramasinghe

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GTP-Cyclohydrolase I deficiency presenting as malignant hyperphenylalaninemia, recurrent hyperthermia and progressive neurological dysfunction in a South Asian child - a case repor... by Kavinda Chandimal Dayasiri, Nayani Suraweera, Deepal Nawarathne, U. E. Senanayake, B. K. T. P. Dayanath, Eresha Jasinge, Kumudu Weerasekara

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Phenotypic spectrum and genetic heterogeneity of cystic fibrosis in Sri Lanka by Neluwa Liyanage Ruwan Indika, Dinesha Maduri Vidanapathirana, Hewa Warawitage Dilanthi, Grace Angeline Malarnangai Kularatnam, Nambage Dona Priyani Dhammika Chandrasiri, Eresha Jasinge

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Lipoprotein Lipase Deficiency in an Infant With Chylomicronemia, Hepatomegaly, and Lipemia Retinalis by Dinesha Maduri Vidanapathirana MBBS, Dip Chem Path, Thushara Rodrigo MBBS, DCH, Samantha Waidyanatha MBBS, MD, MRCP (UK), Eresha Jasinge MBBS, Dip Chem Path, MD, Amanda J. Hooper BSc (Hons), John R. Burnett MBChB, MD, PhD, FRCPA

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