Shige Wang
Shanghai, 200233, China
Last Updated: 09/26/2026
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Found 9 publications
An Electroencephalography Profile of Paroxysmal Kinesigenic Dyskinesia.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: September 03, 2023
Adult-onset neuronal intranuclear inclusion disease related retinal degeneration: a Chinese case series.
Journal: Frontiers in medicine
Published: March 17, 2023
Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia.
Journal: Journal of neurology
Published: November 23, 2021
Expanding the clinical spectrum of adult-onset neuronal intranuclear inclusion disease.
Journal: Acta neurologica Belgica
Published: December 01, 2020
Variants in LAMC3 Causes Occipital Cortical Malformation.
Journal: Frontiers in genetics
Published: October 13, 2020
c.1263+1G>A Is a Latent Hotspot for CYP27A1 Mutations in Chinese Patients With Cerebrotendinous Xanthomatosis.
Journal: Frontiers in genetics
Published: February 04, 2020
Novel mutation of the PRRT2 gene in two cases of paroxysmal kinesigenic dyskinesia: Two case reports.
Journal: Biomedical reports
Published: October 14, 2019
Excessive Startle with Novel GLRA1 Mutations in 4 Chinese Patients and a Literature Review of GLRA1-Related Hyperekplexia.
Journal: Journal of clinical neurology (Seoul, Korea)
Published: July 19, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026