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Pediatric Neurology|July 9, 2010
Childhood chronic inflammatory demyelinating polyneuropathy with nonuniform pathologic featuresXinghua Luan, Riliang Zheng, Bin Chen, et al.Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 28, 2009
The overlap of corticobasal degeneration and Alzheimer changes: an autopsy caseWei Zhang, Riliang Zheng, Zhaoxia Wang, et al.Neuropathology : Official Journal of the Japanese Society of Neuropathology|December 17, 2008
Tubular aggregates in paralysis periodica paramyotonica with T704M mutation of SCN4AXinghua Luan, Bin Chen, Yang Liu, et al.Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 28, 2009
Clincial and pathological study of distal motor neuropathy with N88S mutation in BSCL2Bin Chen, Riliang Zheng, Xinghua Luan, et al.Molecular Genetics and Metabolism Reports|December 6, 2023
The diagnostic journey for patients with late-onset GM2 GangliosidosesMariah C Lopshire, Cynthia Tifft, John Burns, et al.Advances in Therapy|May 27, 2024
Qualitative Study of the Patient Experience with Venglustat for Gaucher Disease Type 3 in a Phase 2 Open-Label, Multicenter, Multinational Study (LEAP)Raphael Schiffmann, Eugen Mengel, Mary Wallace, et al.Journal of Human Genetics|August 19, 2011
Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodesDanhua Zhao, Daojun Hong, Wei Zhang, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 18, 2025
Venglustat in GM2 gangliosidoses and related disorders: Results of the AMETHIST randomized controlled and basket trialsCynthia J Tifft, Isabela Batsu, Roberto Giugliani, et al.Pageof 1