Showing results (41-50 of 98) with videos related to

Sort By:
Pageof 10
Journal of the Neurological Sciences|September 23, 2008
The co-occurrence of serologically proven myasthenia gravis and Miller Fisher/Guillain Barré overlap syndrome: a case reportKwok Kwong Lau, Khean Jin Goh, Han Chih Hencher Lee, et al.
Epilepsy & Behavior : E&B|January 15, 2013
A web-based survey of attitudes toward epilepsy in secondary and tertiary students in Malaysia, using the Public Attitudes Toward Epilepsy (PATE) scaleKheng Seang Lim, Michael D Hills, Wan Yuen Choo, et al.
Epilepsy Research|July 27, 2013
Attitudes toward epilepsy among the primary and secondary school teachers in Malaysia, using the public attitudes toward epilepsy (PATE) scaleKheng Seang Lim, Michael D Hills, Wan Yuen Choo, et al.
Clinical Neurology and Neurosurgery|February 4, 2025
Ictal SPECT success rate using a single SPECT session protocolZheng-Yang Lee, Kheng-Seang Lim, Si-Lei Fong, et al.
The American Journal of Tropical Medicine and Hygiene|January 15, 2014
Sarcocystis nesbitti infection in human skeletal muscle: possible transmission from snakesYee Ling Lau, Phooi Yee Chang, Chong Tin Tan, et al.
Seizure|April 3, 2021
Mortality in adult epilepsy patients in Malaysia: a hospital-based studySi Bao Khor, Kheng-Seang Lim, Si-Lei Fong, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 23, 2002
Nipah encephalitis outbreak in Malaysia, clinical features in patients from SerembanHeng Thay Chong, Sree Raman Kunjapan, Tarmizi Thayaparan, et al.
Annals of Indian Academy of Neurology|August 21, 2018
Differentiating Extensor Plantar Response in Pathological and Normal PopulationShweh Fern Loo, Nicole Kelsie Justin, Ri An Lee, et al.
Epilepsy Research|February 18, 2022
Cause of mortality among people with epilepsy in Malaysia: A hospital-based studySi-Bao Khor, Kheng-Seang Lim, Si-Lei Fong, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 14, 2019
Whole exome sequencing identifies a novel SCN1A mutation in genetic (idiopathic) generalized epilepsy and juvenile myoclonic epilepsy subtypesChung-Kin Chan, Joyce Siew-Yong Low, Kheng-Seang Lim, et al.
Pageof 10