Upload Avatar (500 x 500)
Zu-Neng Lu
lzn196480@126.com
Chinese, English
Hubei
Wuhan University
Medical School
  • 1980.09-1985.07 Bachelor of Clinical Medicine, Wuhan University
  • 1985.09-1988.07 Master of Clinical Medicine, Wuhan University
  • 1993.09-1996.07 PhD in Neurology, Peking Union Medical College Hospital
  • Published over 200 papers, including more than 30 SCI papers
  • Edited and contributed to several neurology textbooks
  • 1988.07-1997.07 Resident, Chief Resident, Attending Physician, Dept. of Neurology, Renmin Hospital, Wuhan University
  • 1997.10-2001.11 Associate Chief Physician, Associate Professor, Dept. of Neurology, Renmin Hospital, Wuhan University
  • 2001.09-2001.12 Visiting Scholar, Nancy University Medical School, France
  • 2001.12--Present Chief Physician, Dept. of Neurology, Renmin Hospital, Wuhan University
  • 2002.10--Present Professor, Dept. of Neurology, Renmin Hospital, Wuhan University
  • 2001 Hubei Province Science and Technology Progress Second Prize for 'The Application Value of Quantitative Study of Motor Units in Neuromuscular Diseases'
  • 2007 Hubei Province Science and Technology Progress Second Prize for 'The Application of Neurophysiological Techniques in Neuromuscular Diseases'
Clinical and basic research of neuropathies and muscular disorders
Clinical electromyography and evaluation in neuromuscular disorders
  • The dynamic expression of canonical Wnt/β-catenin signalling pathway in the pathologic process of experimental autoimmune neuritis, Liu Y, ..., Lu Z, 2020
  • Can the large-scale decrement in repetitive nerve stimulation be used as an exclusion criterion for amyotrophic lateral sclerosis?, Shang L, Chu H, Lu Z, 2020
  • Mapping optogenetically-driven single-vessel fMRI with concurrent neuronal calcium recordings in the rat hippocampus, Chen X, Sobczak F, Chen Y, Jiang Y, Qian C, Lu Z, Ayata C, Logothetis NK, Yu X, 2019
Neuropathies Muscular Disorders Clinical Research Electromyography Guillain-Barre Syndrome Neuromuscular Diseases Pathological Diagnosis Genetic Diagnosis Spinocerebellar Ataxia Molecular Mechanisms

Contact us

Let's talk!
* Required
* Required
* Required
* Invalid email address
By submitting this form, you agree that IoT ONE may contact you with insights and marketing messaging.
No thanks, I don't want to receive any marketing emails from IoT ONE.
Submit

Thank you for your message!
We will contact you soon.