Xiaotun M. Ren
Ueruemqi, 830091, China
Last Updated: 09/26/2026
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Found 37 publications
Electroencephalographic and neuroimaging prognosticators in pediatric FIRES with claustrum lesions: A 21-case retrospective study.
Journal: Seizure
Published: June 21, 2026
Pragmatic Phenotype-Electrophysiology-Genomics Integration in Pediatric Congenital Myasthenic Syndromes: Insights From 36 Patients in a Single-Center Study in China.
Journal: CNS neuroscience & therapeutics
Published: June 21, 2026
Genetic screening of EIF2B genes reveals mutation spectrum and predicted prevalence of vanishing white matter disease in Chinese population.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: January 27, 2026
Live-Cell-Based Assay Outperforms Fixed Assay in MOGAD Diagnosis: A Retrospective Validation Against the 2023 International Criteria.
Journal: Diagnostics (Basel, Switzerland)
Published: November 07, 2025
Soluble TREM2 Is Elevated in Pediatric Patients with Anti-NMDAR Encephalitis.
Journal: Journal of clinical medicine
Published: October 19, 2025
The symmetrical claustrum sign in pediatric febrile infection-related epilepsy syndrome: Diagnostic value and clinical implications.
Journal: Epilepsia
Published: August 23, 2025
Pathogenic mechanisms and clinical insights into B3GALNT2-related alpha-dystroglycanopathies.
Journal: Journal of neuromuscular diseases
Published: July 16, 2025
Clinical, imaging, and recurrence analysis of myelin oligodendrocyte glycoprotein antibody-associated disease with initial presentation as meningoencephalitis in children: a single-center retrospective study.
Journal: Pediatric radiology
Published: February 05, 2025
Effectiveness and safety of perampanel for pediatric patients with epilepsy: A real-world study from China.
Journal: Pediatric investigation
Published: April 26, 2024
Phenotypic spectrum of iron-sulfur cluster assembly gene IBA57 mutations: c.286 T > C identified as a hotspot mutation in Chinese patients with a stable natural history.
Journal: Journal of human genetics
Published: March 10, 2024
Neurophenotype and genetic analysis of children with Aicardi-Goutières syndrome in China.
Journal: Pediatric investigation
Published: November 29, 2023
Encephalitis is an Important Phenotype of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Diseases: A Single-Center Cohort Study.
Journal: Pediatric neurology
Published: May 15, 2023
Last Updated: 09/26/2026