Hai-yan Zhou
197 Rui Jin Er Road
Shanghai, 200025, China
Shanghai, 200025, China
Last Updated: 09/26/2026
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Found 22 publications
Case report: Hereditary spastic paraplegia with a novel homozygous mutation in ZFYVE26.
Journal: Frontiers in neurology
Published: February 06, 2023
Increased functional connectivity of white-matter in myotonic dystrophy type 1.
Journal: Frontiers in neuroscience
Published: May 28, 2022
Altered Local Brain Amplitude of Fluctuations in Patients With Myotonic Dystrophy Type 1.
Journal: Frontiers in aging neuroscience
Published: October 07, 2021
Sex effects on clinical features in LRRK2 G2385R carriers and non-carriers in Parkinson's disease.
Journal: BMC neuroscience
Published: September 10, 2020
Altered structural and functional connectivity in CSF1R-related leukoencephalopathy.
Journal: Brain imaging and behavior
Published: July 25, 2020
New phenotype of DCTN1-related spectrum: early-onset dHMN plus congenital foot deformity.
Journal: Annals of clinical and translational neurology
Published: November 22, 2019
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
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
Last Updated: 09/26/2026