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Dr Dinesha Maduri Vidanapathirana
Dr Dinesha Maduri Vidanapathirana
Senior Lecturer in Chemical Pathology/Consultant Chemical Pathologist,Faculty of Medical Sciences
Verified email at sjp.ac.lk
Title
Cited by
Cited by
Year
Phenotypic spectrum and genetic heterogeneity of cystic fibrosis in Sri Lanka
NLR Indika, DM Vidanapathirana, HW Dilanthi, GAM Kularatnam, ...
BMC Medical Genetics 20, 1-7, 2019
152019
Many pitfalls in diagnosis of acute intermittent porphyria: a case report
NLR Indika, T Kesavan, HW Dilanthi, K Jayasena, N Chandrasiri, ...
BMC Research Notes 11, 1-5, 2018
142018
Dubin–Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report
GAM Kularatnam, D Warawitage, DM Vidanapathirana, S Jayasena, ...
BMC research notes 10, 1-5, 2017
142017
Lipin-1 deficiency-associated recurrent rhabdomyolysis and exercise-induced myalgia persisting into adulthood: a case report and review of literature
NLR Indika, DM Vidanapathirana, E Jasinge, R Waduge, NLA Shyamali, ...
Case Reports in Medicine 2020, 2020
112020
A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia
DM Vidanapathirana, S Jayasena, E Jasinge, B Stiburkova
BMC pediatrics 18, 1-5, 2018
112018
Uric acid, an important screening tool to detect inborn errors of metabolism: a case series
E Jasinge, GAM Kularatnam, HW Dilanthi, DM Vidanapathirana, ...
BMC research notes 10, 1-6, 2017
102017
Association of serum uric acid and gamma-glutamyltransferase with obesity related metabolic derangements in a cohort of children with obesity in Sri Lanka
DM Vidanapathirana, EA Jasinge, D Saramanayake, P Wickramasinghe
Ceylon Med J 64, 125-32, 2019
52019
Identification of a novel MTTP splice variant c. 394-2A> C in an infant with abetalipoproteinemia
DM Vidanapathirana, E Jasinge, S Waidyanatha, AJ Hooper, JR Burnett
J Rare Dis Res Treat 4 (2), 25-27, 2019
22019
Lipoprotein Lipase Deficiency in an Infant With Chylomicronemia, Hepatomegaly, and Lipemia Retinalis
DM Vidanapathirana, T Rodrigo, S Waidyanatha, E Jasinge, AJ Hooper, ...
Global Pediatric Health 4, 2333794X17715839, 2017
22017
Corrigendum to: Urine Organic Acid Analysis: Key Diagnostic Test for Fumaric Aciduria in a Sri Lankan Child
E Jasinge, M Fernando, NLR Indika, R Trunzo, S Schröder, ...
Labmedicine 53 (3), e62, 2022
12022
A case of molybdenum cofactor deficiency
DM Vidanapathirana, S Jayasena, EA Jasinge, P Ratnayake, L Fairbanks
Sri Lanka Journal of Child Health 46 (3), 273-274, 2017
12017
Molybdenum Cofactor Deficiency (MoCD): Complementation Groups A–C
DM Vidanapathirana, E Jasinge, AL Misko
Genetic Syndromes: A Comprehensive Reference Guide, 1-6, 2023
2023
Clinical and demographic characteristics of organic acidaemias in children in a tertiary care hospital in Sri Lanka: A 4-year experience in a single centre
DM Vidanapathirana, PMS Fernando, K Jayasena, N Chandrasiri, ...
Sri Lanka Journal of Child Health 52 (3), 307-313, 2023
2023
Genotypes and phenotypes of Sri Lankan Patients with Mucopolysaccharidosis type IVA
NL Indika, R Indika, A Rolfs, C Beetz, S Schröder, C Pereira, V Volha, ...
Journal of Nepal Paediatric Society 42 (2), 80-82, 2022
2022
Case Report Lipin-1 Deficiency-Associated Recurrent Rhabdomyolysis and Exercise-Induced Myalgia Persisting into Adulthood: A Case Report and Review of Literature
NLR Indika, DM Vidanapathirana, E Jasinge, R Waduge, NLA Shyamali, ...
2020
Lipin-1 deficiency associated recurrent rhabdomyolysis and exercise-induced myalgia persisting into adulthood; A case report and a short review of literature
DM Vidanapathirana, E Jasinge, R Waduge, NLA Shyamali, PPR Perera
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