Liu Gonglu, Ph.D.

Position:Vice Chair of Medical Genetics

DepartmentNeurology

Medical School:Zhejiang University School of Medicine, China

Academic Rank:Associate Chief Physician


Appointment

Clinical / Research Interests

Diagnosis and treatment of neuromuscular diseases, including various types of muscular dystrophy, metabolic myopathy, inflammatory myopathy, peripheral neuropathy, and myasthenia gravis et al.

Professional Highlights

Professional Appointments

Secretary, Basic and Clinical Neurology Group, Chinese Society of Neuroscience 

Member, Myopathy Group, Chinese Society of Neurology, Zhejiang Medical Association


Education Experience

Research Summary

Hereditary myopathy including LGMD2B and distal myopathy.

Publications

Liu G, Ni W, Wang H, Li H, Zhang Y, Wang N, Wu Z, Clinical features of familial amyloid polyneuropathy carrying transthyretin mutations in four Chinese kindreds, J Peripher Nerv Syst, 2017, 22(1):19-26. 

Liu ZJ, Lin HX, Liu GL, Tao QQ, Ni W, Xiao BG, Wu ZY, The investigation of genetic and clinical features in Chinese patients with juvenile amyotrophic lateral sclerosis, Clin Genet, 2017, 92(3):267-273.

Li LX, Liu GL, Liu ZJ, Lu C, Wu ZY, Identification and functional characterization of two missense mutations in NDRG1 associated with Charcot-Marie-Tooth disease type 4D, Hum Mutat, 2017, 38(11):1569-1578.

Liu GL, Wang KY, Guo H, Zhao SJ, Shen Y, Zhao YB, Inositol-requiring protein 1α signaling pathway is activated in the temporal cortex of patients with mesial temporal lobe epilepsy, Neurological Science, 2013,34(3):357-364.

Gonglu Liu, Kaiyan Wang, Chuanzhen Lv, Jun Zhao, Xingdang Liu, Chuantao Zuo, Functional imaging and pathology in brain of interictal cats kindled by pentylenetetrazol, Neurology Asia, 2013,18(1):9-15.


Current Program

Study on the molecular mechanism of endoplasmic reticulum stress-related degradation  pathway in the pathogenesis of limb girdle muscular dystrophy 2B. Funding Source: Natural Science Foundation of Zhejiang.

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