Xiao-jun Huang
Shanghai, China
Last Updated: 09/26/2026
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Found 21 publications
The Pathogenesis of Paroxysmal Kinesigenic Dyskinesia: Current Concepts.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 09, 2022
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample Study.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 21, 2021
Case Report: Neuronal Intranuclear Inclusion Disease With Oromandibular Dystonia Onset.
Journal: Frontiers in neurology
Published: October 17, 2020
Altered structural and functional connectivity in CSF1R-related leukoencephalopathy.
Journal: Brain imaging and behavior
Published: July 25, 2020
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 21, 2019
Novel mutations in the SPAST gene cause hereditary spastic paraplegia.
Journal: Parkinsonism & related disorders
Published: June 08, 2019
Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathy.
Journal: Translational neurodegeneration
Published: January 20, 2019
Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review.
Journal: Neuromuscular disorders : NMD
Published: July 11, 2018
The study of exercise tests in paroxysmal kinesigenic dyskinesia.
Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Published: May 29, 2018
Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature review.
Journal: Seizure
Published: November 02, 2017
Depression, anxiety, and quality of life in paroxysmal kinesigenic dyskinesia patients.
Journal: Chinese medical journal
Published: August 25, 2017
Last Updated: 09/26/2026