Ying Zheng
Fuan, China
Last Updated: 09/26/2026
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Found 8 publications
De Novo Facioscapulohumeral Muscular Dystrophy: A Severe Subtype Driven by D4Z4 Repeat Contractions.
De Novo Facioscapulohumeral Muscular Dystrophy: A Severe Subtype Driven by D4Z4 Repeat Contractions.
Journal: Neurology. Genetics
Published: November 10, 2025
Association of Diaphragm Involvement Assessed by Ultrasound With Disease Severity in Facioscapulohumeral Muscular Dystrophy.
Journal: Journal of cachexia, sarcopenia and muscle
Published: September 11, 2024
Age at onset mediates genetic impact on disease severity in facioscapulohumeral muscular dystrophy.
Journal: Brain : a journal of neurology
Published: April 25, 2024
Comprehensive Proteomic Analysis of Dysferlinopathy Unveiling Molecular Mechanisms and Biomarkers Linked to Pathological Progression.
Journal: CNS neuroscience & therapeutics
Published: April 11, 2024
An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1.
Journal: Brain : a journal of neurology
Published: April 04, 2023
Follicle-stimulating hormone is negatively associated with nonalcoholic fatty liver disease in a Chinese elderly population: a retrospective observational study.
Journal: BMC endocrine disorders
Published: December 20, 2022
Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy.
Journal: Neurology
Published: November 29, 2022
Showing 1-8 of 8
Last Updated: 09/26/2026