Paroxysmal kinesigenic dyskinesia
AT Alibhoy, S Wijemanne, R Gamage Ceylon Medical Journal 51: 36-37 2006http://doi.org/10.4038/cmj.v51i1.1377
Management of West syndrome during COVID-19 pandemic: A viewpoint from South Asian West Syndrome Research Group
JK Sahua, P Madaana, P Chandb, A Kumarc, K Linnd, ML Mynak, P Poudel, J Wanigasinghe Epilepsy Research 167 (2020) 2020https://doi.org/10.1016/j.eplepsyres.2020.106453
Effects of Intra-Subject Variation in Gait Analysis on ASD Classification Performance in Machine Learning Models
B Henderson, P Yogarajah, B Gardiner, M McGinnity, K Forster, B Nicholas, D Wimpory, J Wanigasinghe IEEE Xplore 2020https://doi.org/10.1109/ISSC49989.2020.9180201
Protocol for the Sri Lankan Cerebral Palsy Register pilot study
TM Heiyanthuduwage, SP Sumanasena, G Kitnasamy, HS Sheedy, G Khandaker, R Fernando, S Wijesekara, J Jagoda, P Ratnayake, J Wanigasinghe, S Mclntyre, S Goldsmith, E Waight, N Badawi, M Muhit, N Muttiah BMJ Open 10:e039353 2020http://dx.doi.org/10.1136/bmjopen-2020-039353
Diagnosis and treatment of infantile spasms
J Wanigasinghe Sri Lanka Journal of Child Health 39: 141-145 2010http://doi.org/10.4038/sljch.v39i4.2480
The spectrum of deletions and duplications in the dystrophin (DMD) gene in a cohort of patients with Duchenne muscular dystrophy in Sri Lanka
N Thakur, G Abeysekera, J Wanigasinghe, VHW Dissanayake Neurology India 67: 714-716 2019https://doi.org/10.4103/0028-3886.263235
Age, sex and ethnic differentials in the prevalence and control of epilepsy among Sri Lankan children: a population-based study
J Wanigasinghe, C Arambepola, R Murugupillai, T Chang British Medical Journal Paediatrics Open 2019https://doi.org/10.1136/bmjpo-2018-000430
Benign familial neonatal convulsions: a case report
N Pratheep, J Wanigasinghe Sri Lanka Journal of Child Health 47: 364-365 2018http://doi.org/10.4038/sljch.v47i4.8603
Dopa-responsive dystonia and its diagnostic challenges: a case report
LK Weerasooriya, J Wanigasinghe Sri Lanka Journal of Child Health 47: 268-270 2018http://doi.org/10.4038/sljch.v47i3.8551
Gillespie syndrome in a South Asian child: a case report with confirmation of a heterozygous mutation of the ITPR1 gene and review of the clinical and molecular features
D De Silva, KA Williamson, KC Dayasiri, N Suraweera, V Quinters, H Abeysekara, J Wanigasinghe, D De Silva, H De Silva BMC Pediatrics 18: e308 2018https://doi.org/10.1186/s12887-018-1286-5
