Chujun Wu
Beijing, 100070, China
Last Updated: 09/26/2026
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Found 9 publications
A strategy of microglia replacement alleviates microgliopathy in a CSF1R I794T hotspot mutation mouse model of CSF1R-related disorder.
Journal: Cell reports. Medicine
Published: February 26, 2025
Evaluation of Soluble Colony Stimulating Factor 1 Receptor (CSF1R) in Peripheral Blood as a Diagnostic Marker of CSF1R-Related Disorder (CSF1R-RD) in a Murine Model and CSF1R-RD Patients.
Journal: Annals of neurology
Published: September 20, 2024
The genetic and phenotypic spectra of adult genetic leukoencephalopathies in a cohort of 309 patients.
Journal: Brain : a journal of neurology
Published: June 14, 2022
Serum Neurofilament Light Chain Levels May Be a Marker of Lower Motor Neuron Damage in Amyotrophic Lateral Sclerosis.
Journal: Frontiers in neurology
Published: December 16, 2021
Metachromatic Leukodystrophy: Too Frequent (Mis)Diagnosis?-Reply.
Journal: JAMA neurology
Published: August 15, 2018
Two rare variants of the ANXA11 gene identified in Chinese patients with amyotrophic lateral sclerosis.
Journal: Neurobiology of aging
Published: February 13, 2018
Serial Magnetic Resonance Imaging Changes in a Patient With Late-Onset Cobalamin C Disease With a Misdiagnosis of Metachromatic Leukodystrophy.
Journal: JAMA neurology
Published: January 18, 2018
A Novel Missense Mutation of the DDHD1 Gene Associated with Juvenile Amyotrophic Lateral Sclerosis.
Journal: Frontiers in aging neuroscience
Published: September 08, 2016
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Last Updated: 09/26/2026