Wotu Tian
600 Yishan Road
Shanghai, 200233, China
Shanghai, 200233, China
Last Updated: 09/26/2026
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Found 28 publications
Clinical and functional analysis of KIF5A related spastic paraplegia type 10.
Journal: Parkinsonism & related disorders
Published: May 25, 2025
Efgartigimod Combined With Steroid Treatment for HAM/TSP: A Case Report.
Journal: Annals of clinical and translational neurology
Published: April 26, 2025
Heterozygous KCNJ10 Variants Affecting Kir4.1 Channel Cause Paroxysmal Kinesigenic Dyskinesia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 16, 2024
Clinical and genetic characteristics in a Chinese cohort of complex spastic paraplegia type 4.
Journal: Clinical genetics
Published: December 09, 2023
The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 18, 2023
An Electroencephalography Profile of Paroxysmal Kinesigenic Dyskinesia.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: September 03, 2023
Clinical and Genetic Spectrum in a Large Cohort of Hereditary Spastic Paraplegia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 25, 2023
A novel DCTN1 mutation causing perry syndrome leads to abnormal splicing of mRNA: genetic and functional analyses.
Journal: Acta neurologica Belgica
Published: March 29, 2023
Episodic Neurological Dysfunction in X-Linked Charcot-Marie-Tooth Disease: Expansion of the Phenotypic and Genetic Spectrum.
Journal: Journal of clinical neurology (Seoul, Korea)
Published: March 17, 2023
PLP1 gene mutations cause spastic paraplegia type 2 in three families.
Journal: Annals of clinical and translational neurology
Published: September 17, 2022
Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in HSPB1 Gene: A Case Series.
Journal: Biomolecules
Published: August 12, 2022
Last Updated: 09/26/2026