Zhixian Ye
Fuzhou, 350005, China
Last Updated: 09/26/2026
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Found 11 publications
Corrigendum to "Biomarker profile of a Chinese ALS cohort: A comprehensive clinical-biomarkers-imaging analysis".
Journal: Neurobiology of disease
Published: August 31, 2025
Association of spinal cord structure with cognition in hereditary spastic paraplegia type 5.
Journal: Frontiers in neurology
Published: June 25, 2025
Biomarker profile of a Chinese ALS cohort: A comprehensive clinical-biomarkers-imaging analysis.
Journal: Neurobiology of disease
Published: May 16, 2025
Apolipoprotein E epsilon4 allele is associated with better performance language and visual memory in spinocerebellar ataxia type 3.
Journal: European journal of neurology
Published: July 10, 2024
Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study.
Journal: The Lancet regional health. Western Pacific
Published: January 13, 2022
Correction to: Potential markers for sample size estimations in hereditary spastic paraplegia type 5.
Journal: Orphanet journal of rare diseases
Published: October 28, 2021
Reprogramming of adult human peripheral blood mononuclear cells into hiPSCs from two patients with facioscapulohumeral muscular dystrophy type 1.
Journal: Stem cell research
Published: August 05, 2021
Potential markers for sample size estimations in hereditary spastic paraplegia type 5.
Journal: Orphanet journal of rare diseases
Published: May 26, 2021
Clinical and genetic features of somatic mosaicism in facioscapulohumeral dystrophy.
Journal: Journal of medical genetics
Published: October 17, 2019
Clinical and genetic characterization of limb girdle muscular dystrophy R7 telethonin-related patients from three unrelated Chinese families.
Journal: Neuromuscular disorders : NMD
Published: August 02, 2019
Showing 1-11 of 11
Last Updated: 09/26/2026