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Amyotrophic lateral sclerosis and motor neuron syndromes in Asia

Authors
Shahrizaila, N.Sobue, G.Kuwabara, S.Kim, Seung HyunBirks, CarolFan, D. S.Bae, J. S.Hu, C. J.Gourie-Devi, M.Noto, Y.Shibuya, K.Goh, K. J.Kaji, R.Tsai, C. P.Cui, L.Talman, P.Henderson, R. D.Vucic, S.Kiernan, M. C.
Issue Date
Aug-2016
Publisher
BMJ Publishing Group
Citation
Journal of Neurology, Neurosurgery and Psychiatry, v.87, no.8, pp 821 - 830
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
Journal of Neurology, Neurosurgery and Psychiatry
Volume
87
Number
8
Start Page
821
End Page
830
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/154180
DOI
10.1136/jnnp-2015-312751
ISSN
0022-3050
1468-330X
Abstract
While the past 2 decades have witnessed an increasing understanding of amyotrophic lateral sclerosis (ALS) arising from East Asia, particularly Japan, South Korea, Taiwan and China, knowledge of ALS throughout the whole of Asia remains limited. Asia represents >50% of the world population, making it host to the largest patient cohort of ALS. Furthermore, Asia represents a diverse population in terms of ethnic, social and cultural backgrounds. In this review, an overview is presented that covers what is currently known of ALS in Asia from basic epidemiology and genetic influences, through to disease characteristics including atypical phenotypes which manifest a predilection for Asians. With the recent establishment of the Pan-Asian Consortium for Treatment and Research in ALS to facilitate collaborations between clinicians and researchers across the region, it is anticipated that Asia and the Pacific will contribute to unravelling the uncertainties in ALS.
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서울 의과대학 (DEPARTMENT OF NEUROLOGY)
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