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Clinical Neuropathology|February 11, 2019
Clinical findings and autophagic pathology in neutral lipid storage disease with myopathyDaojun Hong, Junjun Zheng, Ling Xin, et al.
Journal of Clinical Neurology (Seoul, Korea)|January 5, 2024
Episodic Neurological Dysfunction in X-Linked Charcot-Marie-Tooth Disease: Expansion of the Phenotypic and Genetic SpectrumFeixia Zhan, Wotu Tian, Yuwen Cao, et al.
Metabolic Brain Disease|October 28, 2021
Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndromeFeixia Zhan, Xiaoli Liu, Ruilong Ni, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 12, 2010
NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASILZhaoxia Wang, Yun Yuan, Wei Zhang, et al.
Frontiers in Medicine|January 30, 2024
Adult-onset neuronal intranuclear inclusion disease related retinal degeneration: a Chinese case seriesChaoyi Feng, Qian Chen, Xinghua Luan, et al.
Frontiers in Genetics|August 6, 2021
Variants in <i>LAMC3</i> Causes Occipital Cortical MalformationXiaohang Qian, Xiaoying Liu, Zeyu Zhu, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|July 22, 2021
Development of EQ-6, a Novel Analogue of Ethoxyquin to Prevent Chemotherapy-Induced Peripheral NeuropathyAysel Cetinkaya-Fisgin, Jing Zhu, Xinghua Luan, et al.
Journal of Clinical Laboratory Analysis|November 16, 2023
Cryptic exon activation caused by a novel deep-intronic splice-altering variant in Becker muscular dystrophyZhiying Xie, Yunlong Lu, Chang Liu, et al.
The Journal of Investigative Dermatology|January 21, 2014
Localization of serine racemase and its role in the skinRan Inoue, Yoko Yoshihisa, Yosuke Tojo, et al.
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