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Brain : a Journal of Neurology|April 4, 2017
A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathyPei-Chien Tsai, Bing-Wen Soong, Inès Mademan, et al.
The Journal of Headache and Pain|August 31, 2023
Status of diagnosis and preventative treatment for primary headache disorders: real-world data of unmet needs in ChinaHuanxian Liu, Ming Dong, Kaiming Liu, et al.
Headache|January 18, 2023
The prevalence and clinical features of fibromyalgia in Chinese hospital patients with primary headache: The survey of fibromyalgia comorbid with headacheZhao Dong, Kaiming Liu, Huanxian Liu, et al.
Obesity Facts|April 3, 2024
Association between Body Mass Index and Medication-Overuse Headache among Individuals with Migraine: A Cross-Sectional StudyHuanxian Liu, Hongru Zhao, Kaiming Liu, et al.
Cell Reports|July 27, 2012
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsionsHsien-Yang Lee, Yong Huang, Nadine Bruneau, et al.
Neurobiology of Aging|December 27, 2016
ATXN2 trinucleotide repeat length correlates with risk of ALSWilliam Sproviero, Aleksey Shatunov, Daniel Stahl, et al.
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