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Clinical Neuropathology|October 6, 2012
A novel heterozygous deletion-insertion mutation in the desmin gene causes complete atrioventricular block and mild myopathyLingling Cao, Daojun Hong, Min Zhu, et al.Clinical Neuropathology|February 11, 2019
Adult-onset SMALED2 due to a novel <i>BICD2</i> mutation presenting with asymmetrical lower limb involvementChenyi Wan, Yuyao Wang, Qian Zhou, et al.Neural Regeneration Research|September 11, 2014
MAPT as a predisposing gene for sporadic amyotrophic lateral sclerosis in the Chinese Han populationPu Fang, Wenyuan Xu, Chengsi Wu, et al.Annals of Clinical and Translational Neurology|March 5, 2024
Homozygous variant in COQ7 causes autosomal recessive hereditary spastic paraplegiaYusen Qiu, Ying Xiong, Lulu Wang, et al.BMC Neurology|July 1, 2022
Anti-dipeptidyl-peptidase-like protein 6 encephalitis with pure cerebellar ataxia: a case reportJing Lin, Min Zhu, Xiaocheng Mao, et al.Huan Jing Ke Xue= Huanjing Kexue|July 2, 2011
[Evaluation and ecological control of the eutrophic state of Gudong reservoir]Xi-Lu CaoBMC Neurology|September 26, 2021
3,4-diaminopyridine treatment for Lambert-Eaton myasthenic syndrome in adults: a meta-analysis of randomized controlled trialsNa Zhang, Daojun Hong, Taohui Ouyang, et al.Journal of Human Genetics|February 14, 2014
Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases, and a literature review in mainland Chinese patientsMin Zhu, Xuan Zhu, Xueliang Qi, et al.Acta Neuropathologica Communications|June 1, 2022
The polyG diseases: a new disease entityTongling Liufu, Yilei Zheng, Jiaxi Yu, et al.CNS Neuroscience & Therapeutics|June 20, 2025
The Relationship Between Glymphatic Function, White Matter Hyperintensity and Cognition: A Structural Equation Model MRI StudyLin Wu, Kaixiao Chen, Zhi Zhang, et al.Pageof 92