Jingwen Xu
20, Yuhuangding East Road
Yantai, 264000, China
Yantai, 264000, China
Last Updated: 09/26/2026
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Found 17 publications
Adult-onset Sandhoff disease presenting with a motor neuron disease phenotype: clinical and mechanistic insights from patient-derived models.
Journal: Acta neuropathologica communications
Published: October 20, 2025
Clinical and Pathological Features of Vasculitic Neuropathy: A Single-Center Study in China.
Journal: European journal of neurology
Published: September 05, 2025
iPSC-derived microglia: Decoding roles and therapeutic opportunities in neurodegenerative diseases.
Journal: Brain research bulletin
Published: July 22, 2025
CLRN1 Variants in Müller Cells Cause Mitochondrial Dysfunction in USH3A Retinal Organoids.
Journal: CNS neuroscience & therapeutics
Published: October 08, 2024
A Multicenter Study of Hereditary Transthyretin Amyloidosis in China.
Journal: Annals of neurology
Published: September 19, 2024
Skeletal muscle involvement in systemic amyloidosis is often overlooked.
Journal: Neuropathology and applied neurobiology
Published: January 31, 2024
A comparative study on riboflavin responsive multiple acyl-CoA dehydrogenation deficiency due to variants in FLAD1 and ETFDH gene.
Journal: Journal of human genetics
Published: August 12, 2023
Generation of an induced pluripotent stem cell (iPSC) line (INNDSUi002-A) from a patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
Journal: Stem cell research
Published: December 22, 2022
Generation of a human induced pluripotent stem cell line (INNDSUi003-A) derived from patient with Becker muscular dystrophy (BMD).
Journal: Stem cell research
Published: February 24, 2022
Clinical, pathological and genetic features and follow-up of 110 patients with late-onset MADD: a single-center retrospective study.
Journal: Human molecular genetics
Published: July 28, 2021
Last Updated: 09/26/2026