Xingao Wang
Beijing, China
Last Updated: 09/26/2026
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Found 27 publications
Genotypic features of Spinocerebellar Ataxia in Northern China: A Comparative Analysis with Southern China.
Journal: Cerebellum (London, England)
Published: April 28, 2026
Retinal thinning and dorsal visual stream degeneration in neuronal intranuclear inclusion disease: Multimodal MRI/OCT evidence with network and mediation analyses.
Journal: Neurobiology of disease
Published: March 10, 2026
MRI abnormal patterns of lumbar paraspinal muscles in patients with amyotrophic lateral sclerosis and lumbosacral radiculopathy: a comparative study.
Journal: Frontiers in neurology
Published: November 21, 2025
Evolutionary implications of NOTCH2NLC mutations: brain structural changes in neuronal intranuclear inclusion disease revealed by comprehensive morphometry.
Journal: Brain communications
Published: August 27, 2025
Peripheral neuropathy in neuronal intranuclear inclusion disease: a clinical and electrophysiological cross-sectional study.
Journal: Journal of neurology
Published: October 14, 2024
Stroke-like episodes in patients with adult-onset neuronal intranuclear inclusion disease and patients with late-onset MELAS: A comparative study.
Journal: Annals of clinical and translational neurology
Published: July 15, 2024
Clinical spectrum, treatment and outcomes of the m.10197G>A mutation in MT-ND3: a case report, systematic review and meta-analysis.
Journal: Orphanet journal of rare diseases
Published: June 19, 2024
Low HALP (Hemoglobin, Albumin, Lymphocyte, and Platelet) Score Increases the Risk of Post-Stroke Cognitive Impairment: A Multicenter Cohort Study.
Journal: Clinical interventions in aging
Published: July 28, 2023
Dystonia, spastic tetraplegia, and ataxia due to a novel mutation in the dynamin domain of OPA1.
Journal: Annals of clinical and translational neurology
Published: July 21, 2023
Reply to: "Inappropriate interpretation of non-pathogenic HTRA1 variant as pathogenic".
Journal: Annals of clinical and translational neurology
Published: May 14, 2023
Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: August 28, 2022
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
Last Updated: 09/26/2026