Wenjing Hu - Publications

A single-center retrospective analysis of autoimmune glial fibrillary acidic protein astrocytopathy with seizures in children.

Journal: Frontiers in neurology

Published: March 13, 2025

Serum globulin in children with myasthenia gravis: predicting relapse and prognosis.

Journal: Neurological research

Published: April 11, 2024

Different Cortical Activation of Facial Synkinesis Patients with Different Course of Disease: A Task fMRI Study.

Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

Published: December 12, 2023

Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patients.

Journal: Frontiers in neurology

Published: October 09, 2023

Genetic analysis of a child with early onset neurodevelopmental disorder with involuntary movement and a literature review

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: March 27, 2023

Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: March 27, 2023

Leptomeningeal enhancement of myelin oligodendrocyte glycoprotein antibody-associated encephalitis: uncovering novel markers on contrast-enhanced fluid-attenuated inversion recovery images.

Journal: Frontiers in immunology

Published: January 27, 2023

Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children.

Journal: Frontiers in neuroscience

Published: November 23, 2022

Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations.

Journal: Frontiers in neuroscience

Published: October 21, 2022

Nabais Sa-de Vries syndrome in a Chinese infant associated with a novel SPOP mutation: A clinical study and genetic report.

Journal: Molecular genetics & genomic medicine

Published: August 23, 2022

Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort Study.

Journal: Frontiers in pediatrics

Published: February 21, 2022

Enhanced Rotated Mask R-CNN for Chromosome Segmentation.

Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

Published: December 11, 2021