Lingchao Meng

5PUBLICATIONS
13CO-AUTHORS
Medical biochemistry - amino acids and metabolitesNeurology and neuromuscular diseasesGene mappingAerospace engineering not elsewhere classifiedMedical biotechnology diagnostics (incl. biosensors)
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Publications (5)

|Jun 28, 2025
Neuromuscular pathology and mitochondrial dysfunction in sorbitol dehydrogenase gene-related distal hereditary motor neuropathies.

Zhenyu Li, Xujun Chu, Yize Li

|Jun 11, 2025
Chronic inflammatory demyelinating polyneuropathy in end-stage renal disease patients: a case series study.

Yize Li, Yakun Wu, Zhenyu Li

|Feb 20, 2025
A Multicenter Study of Hereditary Transthyretin Amyloidosis in China.

Xujun Chu, Juan Kang, Jingwen Xu

|Sep 13, 2024
Clinical and biochemical characterization of asymptomatic carriers and symptomatic patients with hereditary transthyretin amyloidosis caused by TTR V30L mutation.

Hao Jiao, Mengdie Wang, Kang Du

|Sep 04, 2024
Novel mutation of SMPX-related scapuloperoneal myopathy and myofibrillar myopathy.

Zhenyu Li, Xujun Chu, Yize Li

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Frequent Collaborators

1 joint publications

Yu Liu

1 joint publications

Xujun Chu

1 joint publications

Haishan Jiang

1 joint publications

Zhi-Ying Wu