Dinesha Maduri Vidanapathirana

Phenotypic spectrum and genetic heterogeneity of cystic fibrosis in Sri Lanka

Neluwa-Liyanage R. Indika, Dinesha Maduri Vidanapathirana, Hewa Warawitage Dilanthi et al. · BMC Medical Genetics · 2019 · 22 citations · Full text

Life Sciences, Genetics, Pediatrics +15

Many pitfalls in diagnosis of acute intermittent porphyria: a case report

Neluwa-Liyanage R. Indika, T. M. Ananda Kesavan, Hewa Warawitage Dilanthi et al. · BMC Research Notes · 2018 · 19 citations · Full text

Medicine, Neurology, Iron Metabolism Disorders +14

Lipin-1 Deficiency-Associated Recurrent Rhabdomyolysis and Exercise-Induced Myalgia Persisting into Adulthood: A Case Report and Review of Literature

Neluwa-Liyanage R. Indika, Dinesha Maduri Vidanapathirana, Eresha Jasinge et al. · Case Reports in Medicine · 2020 · 18 citations · Full text

Life Sciences, Biochemistry, Biochemical Genetics +14

Uric acid, an important screening tool to detect inborn errors of metabolism: a case series

Eresha Jasinge, Grace Angeline Malarnangai Kularatnam, Hewa Warawitage Dilanthi et al. · BMC Research Notes · 2017 · 14 citations · Full text

Medicine, Biochemistry, Pediatrics +10

Dubin–Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report

Grace Angeline Malarnangai Kularatnam, Dilanthi Hewa Warawitage, Dinesha Maduri Vidanapathirana et al. · BMC Research Notes · 2017 · 10 citations · Full text

Life Sciences, Biochemistry, Genetics +17