Bin Chen

Tubular aggregates in paralysis periodica paramyotonica with T704M mutation of SCN4A

Wei Zhang, Yun Yuan, X. Luan, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL

H. Lv, Wei Zhang, Zhaoxia Wang, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

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

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

Oculopharyngeal Muscular Dystrophy: Phenotypic and Genotypic Studies in a Chinese Population

Yun Yuan, P. Lin, Chuanzhu Yan, 2014, NeuroMolecular Medicine.

Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Childhood chronic inflammatory demyelinating polyneuropathy with nonuniform pathologic features.

Yun Yuan, X. Luan, Bin Chen, 2010, Pediatric neurology.

Phenotypic patterns of MELAS/LS overlap syndrome associated with m.13513G>A mutation, and neuropathological findings in one autopsy case

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2010, Neuropathology : official journal of the Japanese Society of Neuropathology.

A new pseudoexon activation due to ultrarare branch point formation in Duchenne muscular dystrophy

Wei Zhang, Zhaoxia Wang, Zhiying Xie, 2023, Neuromuscular Disorders.