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European Journal of Rheumatology|August 6, 2026
Nemaline Myopathy in Systemic Lupus ErythematosusRan Cui, Xing-Hua Luan, Sheng-Ming Dai
Clinical & Experimental Ophthalmology|October 29, 2008
Retinal arterial abnormalities correlate with brain white matter lesions in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathyYang Liu, Yuan Wu, Sheng Xie, et al.
Frontiers in Neurology|March 8, 2021
Case Report: Neuronal Intranuclear Inclusion Disease With Oromandibular Dystonia OnsetWei-Ping Deng, Zhao Yang, Xiao-Jun Huang, et al.
Zhonghua Yi Xue Za Zhi|January 23, 2009
[Mitochondrial DNA mutation analysis in 97 Chinese patients with mitochondrial cephalomyopathy]Zhao-xia Wang, Xing-hua Luan, Ying Zhang, et al.
Zhonghua Yi Xue Za Zhi|March 3, 2010
[Two novel mutations of GJB1 gene associated with typical X-linked Charcot-Marie-Tooth disease]Xiao-hui Qiao, Yue-xing Li, Xing-zhi Chang, et al.
Frontiers in Medicine|March 31, 2023
Case report: Muscular tuberculosis with lower-extremity muscular masses as the initial presentation: Clinicopathological analysis of two cases and review of the literatureXiao-Wei Zhu, Xing-Hua Luan, Kai-Li Jiang, et al.
Neuroscience Letters|December 3, 2015
Novel ATM mutations with ataxia-telangiectasiaXiao-Li Liu, Tian Wang, Xiao-Jun Huang, et al.
Annals of Clinical and Translational Neurology|June 19, 2019
Lysosomal degradation of GMPPB is associated with limb-girdle muscular dystrophy type 2TWo-Tu Tian, Hai-Yan Zhou, Fei-Xia Zhan, et al.
Frontiers in Aging Neuroscience|December 27, 2021
Altered Local Brain Amplitude of Fluctuations in Patients With Myotonic Dystrophy Type 1Pei Huang, Xing-Hua Luan, Zhou Xie, et al.
Annals of Clinical and Translational Neurology|February 6, 2020
New phenotype of DCTN1-related spectrum: early-onset dHMN plus congenital foot deformityWo-Tu Tian, Li-Hua Liu, Hai-Yan Zhou, et al.
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