Long Chen
Fuzhou, China
Last Updated: 09/26/2026
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Found 12 publications
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
CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: September 26, 2023
Correction of human nonsense mutation via adenine base editing for Duchenne muscular dystrophy treatment in mouse.
Journal: Molecular therapy. Nucleic acids
Published: July 27, 2023
An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1.
Journal: Brain : a journal of neurology
Published: April 04, 2023
Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy.
Journal: Neurology
Published: November 29, 2022
Expanding the phenotype and genotype spectra of PLIN4-associated myopathy with rimmed ubiquitin-positive autophagic vacuolation.
Journal: Acta neuropathologica
Published: February 22, 2022
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
Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population.
Journal: Brain : a journal of neurology
Published: January 06, 2022
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy.
Journal: Annals of neurology
Published: November 29, 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
Showing 1-12 of 12
Last Updated: 09/26/2026