Riliang Zheng

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 episodes

Danhua Zhao, Daojun Hong, Wei Zhang et al. · Journal of Human Genetics · 2011 · 48 citations

Life Sciences, Genetics, Molecular Genetics +16

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. · Advances in Therapy · 2024 · 17 citations · Full text

Life Sciences, Neurology, Neuroscience +15

Clincial and pathological study of distal motor neuropathy with N88S mutation in BSCL2

Bin Chen, Riliang Zheng, Xinghua Luan et al. · Neuropathology · 2009 · 14 citations

Medicine, Genetics, Neurology +17

Tubular aggregates in paralysis periodica paramyotonica with T704M mutation of <i>SCN4A</i>

Xinghua Luan, Bin Chen, Yang Liu et al. · Neuropathology · 2008 · 12 citations

Medicine, Molecular Genetics, Neurology +10

Childhood Chronic Inflammatory Demyelinating Polyneuropathy With Nonuniform Pathologic Features

Xinghua Luan, Riliang Zheng, Bin Chen et al. · Pediatric Neurology · 2010 · 11 citations

Medicine, Neurology, Pediatrics +14