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Hasani Hewavitharana

ORCID: 0000-0003-4302-1736
Observed ORCID: 0000-0003-4302-1736
OpenAlex ID: A5047439833
Cornea Verticillata in classical Fabry disease, first from Sri Lanka: a case report
2020 · Hasani Hewavitharana, Eresha Jasinge, et al. · BMC Pediatrics · 4
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Wcn25-1066 Renal Glycosuria Due to Slc5a2 Mutation in a Child Presenting With Recurrent Urinary Tract Infections and Failure to Thrive
2025 · Randula Ranawaka, Pushpika Deshapriya, et al. · Kidney International Reports · 1
Functional characterization of genetic variants associated with rare inherited renal disorders in the Sri Lankan population
2026 · K. M. Fathima Rizna, Nafeesa Noordeen, et al. · Molecular Genetics and Genomics
The importance of genetic testing in managing developmental epileptic encephalopathy in resource-limited settings: a case report
2026 · Hashan Pathiraja, Achala Wanasinghe, et al. · Journal of Medical Case Reports
Quality of life and sociodemographic characterisation of Sri Lankan children with Trisomy 21: A case control study
2025 · Hasani Hewavitharana, Ruwangi Dissanayake, et al. · Rare
First reported case of Dent Disease Type 2 in a Trisomy 21 child
2025 · Hasani Hewavitharana, Randula Ranawaka, et al. · Rare
Wcn24-1148 a Novel Mutation at C.1993c>t in Exon 16 of the Daam2 Gene Causing Steroid Resistant Nephrotic Syndrome Achieving Long Term Remission Following Rituximab Therapy
2024 · Randula Ranawaka, Hasani Hewavitharana, et al. · Kidney International Reports
A clinical audit on the screening program and outcome of retinopathy of prematurity at a neonatal intensive care unit & special care baby unit at a tertiary care centre in Sri Lanka
2020 · Hasani Hewavitharana, Surantha Perera, et al. · Journal Of The Postgraduate Institute of Medicine
Works count: 8
Citation count: 5
H-index: 1
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