Xinghua H. Luan
600 Yishan Road
Shanghai, 200233, China
Shanghai, 200233, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 41 publications
Novel proteomics and neuropathology of NOTCH2NLC-related neuronal intranuclear inclusion disease.
Journal: Frontiers in aging neuroscience
Published: March 10, 2026
Coexisting myelin oligodendrocyte glycoprotein antibody-associated disease and spinal dural arteriovenous fistula: A diagnostic and neuroimmunological challenge.
Journal: Journal of neuroimmunology
Published: February 06, 2026
Neuronal intranuclear inclusion disease presenting with recurrent dizziness and headache: a case report with 5-year follow-up.
Journal: Frontiers in genetics
Published: October 05, 2025
Microglia replacement halts the progression of microgliopathy in mice and humans.
Journal: Science (New York, N.Y.)
Published: July 10, 2025
Case Report: A pharmacist-led precision therapy framework for managing invasive fungal infection in CSF1R-Related leukoencephalopathy post Allo-HSCT.
Journal: Frontiers in pharmacology
Published: July 01, 2025
Efgartigimod Combined With Steroid Treatment for HAM/TSP: A Case Report.
Journal: Annals of clinical and translational neurology
Published: April 26, 2025
A Charcot-Marie-Tooth Disease Type 1J Case With Diffuse Thickening of Peripheral Nerves.
Journal: Neurology
Published: January 21, 2025
A Multicenter Study of Hereditary Transthyretin Amyloidosis in China.
Journal: Annals of neurology
Published: September 19, 2024
The Effect of Repetitive Transcranial Magnetic Stimulation of the Dorsolateral Prefrontal Cortex on the Amyotrophic Lateral Sclerosis Patients With Cognitive Impairment: A Double-Blinded, Randomized, and Sham Control Trial.
Journal: CNS neuroscience & therapeutics
Published: September 06, 2024
High-risk screening for late-onset Pompe disease in China: An expanded multicenter study.
Journal: Journal of inherited metabolic disease
Published: June 12, 2024
Novel variants and genotype-phenotype correlation in a multicentre cohort of GNE myopathy in China.
Journal: Journal of medical genetics
Published: May 30, 2024
Heterozygous KCNJ10 Variants Affecting Kir4.1 Channel Cause Paroxysmal Kinesigenic Dyskinesia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 16, 2024
Last Updated: 09/26/2026