Guillain-Barre syndrome of acute motor axonal neuropathy (AMAN) type associated with herpes zoster: a case report
Wanninayake L, Rajapaksha D, Nair N, Gunarathne K, Ranawaka U BMC Neurology 2024;24(1):109 2024
Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go.
Dangouloff T, Vrščaj E, Servais L, Osredkar D; SMA NBS World Study Group. Neuromuscular Disorders Jun;31(6):574-582. 2021
Non familial juvenile distal spinal muscular atrophy of upper extremity
J B Peiris, K N Seneviratne, H R Wickremasinghe, S B Gunatilake, R Gamage Miscellaneous Journal of Neurology, Neurosurgery and Psychiatry 52:314-319 1989https://dx.doi.org/10.1136%2Fjnnp.52.3.314
Association of infection with flaviviruses with occurrence of Guillain-Barre syndrome (GBS)
A Goonatilaka, L Gomes, S Dayarathna, N Malavige, T Chang Journal of the Neurological Sciences 405: e206 2019https://doi.org/10.1016/j.jns.2019.10.1180
Polyneuropathy, organomegaly, endocrinopathy, monoclonal band, and skin (POEMS) changes syndrome presenting with a pseudosensory level: a case report
S Paranavitane, L Gooneratne, T Chang Journal of Medical Case Reports 13: e384 2019https://doi.org/10.1186/s13256-019-2309-z
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
Determining the association of flaviviruses, and arboviruses with GBS in south and south-east Asia
SJA Agustin, T Chang, ILL Yip, B Ng, O Ohnmar, M Saini, L Ng, W Hugh, B Jacobs, N Malavige, T Thomas, S Tanprawate, S Khan, H Nghia, S Keosodsay, S Vorachit, MM Zaw, M Bhattacharya, P Shembalkar, T Umapathi Journal of the Peripheral Nervous System 23: e379 2018
Infantile-onset myelin protein zero-related demyelinating neuropathy presenting as an upper extremity monoplegia
EM Yiu, J Wanigasinghe, MT Mackay, M Gonzales, GA Nicholson, MM Ryan Seminars in Pediatric Neurology 2017https://doi.org/10.1016/j.spen.2017.03.005
A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report
T Chang, J Cossins, D Beeson BMC Neurology 16: e195 2016https://doi.org/10.1186/s12883-016-0716-y
Association of type IV spinal muscular atrophy (SMA) with myoclonic epilepsy within a single family
DS Liyanage, LS Pathberiya, IK Gooneratne, KK Vithanage, R Gamage International Archives of Medicine 7: e42 2014
