Xiuwei Zhuo

Beijing, China

Last Updated: 09/26/2026

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Found 13 publications

Clinical and Neuroimaging Features of Basal Ganglia Encephalitis in Children.

Clinical and Neuroimaging Features of Basal Ganglia Encephalitis in Children.

Journal: Pediatric neurology
Published: April 07, 2026

Phenotypic and genotypic characteristics of children STXBP1-related disorders.

Phenotypic and genotypic characteristics of children STXBP1-related disorders.

Journal: Seizure
Published: January 22, 2026

Copy number variation analysis of cerebrospinal fluid metagenomic next-generation sequencing data in assisting the diagnosis of pediatric brain tumors.

Copy number variation analysis of cerebrospinal fluid metagenomic next-generation sequencing data in assisting the diagnosis of pediatric brain tumors.

Journal: Pediatric investigation
Published: December 20, 2025

Mycoplasma Pneumoniae-Associated Arterial Ischemic Stroke in Pediatric Patients: Clinical Manifestations and Neuroimaging Findings.

Mycoplasma Pneumoniae-Associated Arterial Ischemic Stroke in Pediatric Patients: Clinical Manifestations and Neuroimaging Findings.

Journal: Pediatric neurology
Published: January 18, 2025

Phenotypic and genotypic characteristics of children with PCDH19 clustering epilepsy in China.

Phenotypic and genotypic characteristics of children with PCDH19 clustering epilepsy in China.

Journal: Seizure
Published: April 07, 2024

Genotype and Phenotype Characteristics of 58 Cases of Mitochondrial Epilepsy with Nuclear DNA Mutations in Children.

Genotype and Phenotype Characteristics of 58 Cases of Mitochondrial Epilepsy with Nuclear DNA Mutations in Children.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: March 20, 2024

Clinical characteristics and prognosis of paediatric respiratory syncytial virus-related encephalopathy.

Clinical characteristics and prognosis of paediatric respiratory syncytial virus-related encephalopathy.

Journal: Italian journal of pediatrics
Published: March 04, 2024

Encephalitis is an Important Phenotype of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Diseases: A Single-Center Cohort Study.

Encephalitis is an Important Phenotype of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Diseases: A Single-Center Cohort Study.

Journal: Pediatric neurology
Published: May 15, 2023

De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndrome.

De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndrome.

Journal: Gene
Published: October 04, 2022

Mycophenolate mofetil: An alternative disease-modifying agent for MOG-IgG-associated disorders in childhood: A single-center bidirectional cohort study.

Mycophenolate mofetil: An alternative disease-modifying agent for MOG-IgG-associated disorders in childhood: A single-center bidirectional cohort study.

Journal: Multiple sclerosis and related disorders
Published: March 24, 2022

Cerebral small vessel disease caused by PLOD3 mutation: Expanding the phenotypic spectrum of lysyl hydroxylase-3 deficiency.

Cerebral small vessel disease caused by PLOD3 mutation: Expanding the phenotypic spectrum of lysyl hydroxylase-3 deficiency.

Journal: Pediatric investigation
Published: February 15, 2022

A 5-year-old child presenting with tumor-like primary angiitis of the central nervous system.

A 5-year-old child presenting with tumor-like primary angiitis of the central nervous system.

Journal: Pediatric investigation
Published: October 19, 2021
Showing 1-12 of 13

Last Updated: 09/26/2026