Zeshu Ning

No.86 Ziyuan Road
Changsha, 410007, China

Last Updated: 09/26/2026

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Found 16 publications

A novel de novo QRICH1 variant causing Ververi-Brady syndrome with infantile epileptic spasms syndrome: clinical and genetic analysis.

A novel de novo QRICH1 variant causing Ververi-Brady syndrome with infantile epileptic spasms syndrome: clinical and genetic analysis.

Journal: Frontiers in neuroscience

Published: April 06, 2026

Dynamic temporal partitioning enhanced transformer for pediatric viral load forecasting.

Dynamic temporal partitioning enhanced transformer for pediatric viral load forecasting.

Journal: Frontiers in public health

Published: March 13, 2026

Severe viral rash progression prediction and surveillance early warning based on local-global attention and temporal convolutional network.

Severe viral rash progression prediction and surveillance early warning based on local-global attention and temporal convolutional network.

Journal: Frontiers in public health

Published: January 26, 2026

Retrospective analysis of diagnosis and treatment in 9 cases of childhood-onset methylmalonic acidemia in China.

Retrospective analysis of diagnosis and treatment in 9 cases of childhood-onset methylmalonic acidemia in China.

Journal: Frontiers in neurology

Published: June 07, 2025

Genetic analysis of a child with Leukoencephalopathy with ataxia caused by a homozygous variant of CLCN2 gene and a literature review

Genetic analysis of a child with Leukoencephalopathy with ataxia caused by a homozygous variant of CLCN2 gene and a literature review

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

Published: January 08, 2025

Breath-holding spells comorbidity with epileptic seizures in children: VEEG and clinical outcomes.

Breath-holding spells comorbidity with epileptic seizures in children: VEEG and clinical outcomes.

Journal: Medicine

Published: September 03, 2024

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

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

Journal: Neurological research

Published: April 11, 2024

Clinical and genetic analyses of APMR4 syndrome caused by novel biallelic LSS variants.

Clinical and genetic analyses of APMR4 syndrome caused by novel biallelic LSS variants.

Journal: Frontiers in neuroscience

Published: September 25, 2023

Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study.

Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study.

Journal: Frontiers in immunology

Published: January 09, 2023

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

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

Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study.

Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study.

Journal: Italian journal of pediatrics

Published: September 07, 2022

Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation.

Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation.

Journal: Frontiers in pediatrics

Published: October 25, 2021

Showing 1-12 of 16

Last Updated: 09/26/2026