Hua Wang

39 Huaxiang Road
Shenyang, 110004, China

Last Updated: 09/26/2026

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Found 18 publications

Nusinersen effectiveness and safety in children with type II/III 5q-spinal muscular atrophy: Second interim analysis from a Chinese disease registry.

Nusinersen effectiveness and safety in children with type II/III 5q-spinal muscular atrophy: Second interim analysis from a Chinese disease registry.

Journal: Chinese medical journal

Published: August 30, 2025

Leukemia Inhibitory Factor Attenuates Hypoxic-Ischemic White Matter Injury via NLRP3 Inflammasome Activity Suppressing Through the Nrf2/HO-1 Pathway.

Leukemia Inhibitory Factor Attenuates Hypoxic-Ischemic White Matter Injury via NLRP3 Inflammasome Activity Suppressing Through the Nrf2/HO-1 Pathway.

Journal: Frontiers in bioscience (Landmark edition)

Published: December 27, 2024

The improvement in diagnostic yield of developmental and epileptic encephalopathy by the multi-omics sequential testing method.

The improvement in diagnostic yield of developmental and epileptic encephalopathy by the multi-omics sequential testing method.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: April 23, 2024

Emerging ferroptosis inhibitors as a novel therapeutic strategy for the treatment of neonatal hypoxic-ischemic encephalopathy.

Emerging ferroptosis inhibitors as a novel therapeutic strategy for the treatment of neonatal hypoxic-ischemic encephalopathy.

Journal: European journal of medicinal chemistry

Published: August 01, 2023

Novel KCNC2 variant associated with developmental and epileptic encephalopathy.

Novel KCNC2 variant associated with developmental and epileptic encephalopathy.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: December 05, 2022

Novel Heterozygous Missense Variant in GRIA4 Gene Associated With Neurodevelopmental Disorder With or Without Seizures and Gait Abnormalities.

Novel Heterozygous Missense Variant in GRIA4 Gene Associated With Neurodevelopmental Disorder With or Without Seizures and Gait Abnormalities.

Journal: Frontiers in genetics

Published: January 21, 2022

Leigh Syndrome: A Study of 209 Patients at the Beijing Children's Hospital.

Leigh Syndrome: A Study of 209 Patients at the Beijing Children's Hospital.

Journal: Annals of neurology

Published: September 10, 2021

Comparative study of neonatal brain injury fetuses using machine learning methods for perinatal data.

Comparative study of neonatal brain injury fetuses using machine learning methods for perinatal data.

Journal: Computer methods and programs in biomedicine

Published: May 04, 2021

Positive antithyroid antibody predicts severity of neuromyelitis optica spectrum disorder in children.

Positive antithyroid antibody predicts severity of neuromyelitis optica spectrum disorder in children.

Journal: Multiple sclerosis and related disorders

Published: April 19, 2021

Clinical features of SARS-CoV-2-associated encephalitis and meningitis amid COVID-19 pandemic.

Clinical features of SARS-CoV-2-associated encephalitis and meningitis amid COVID-19 pandemic.

Journal: World journal of clinical cases

Published: November 05, 2020

Usher syndrome type 2A complicated with glycogen storage disease type 3 due to paternal uniparental isodisomy of chromosome 1 in a sporadic patient.

Usher syndrome type 2A complicated with glycogen storage disease type 3 due to paternal uniparental isodisomy of chromosome 1 in a sporadic patient.

Journal: Molecular genetics & genomic medicine

Published: June 01, 2020

Crosstalk between the Ketogenic Diet and Epilepsy: From the Perspective of Gut Microbiota.

Crosstalk between the Ketogenic Diet and Epilepsy: From the Perspective of Gut Microbiota.

Journal: Mediators of inflammation

Published: April 11, 2019

Showing 1-12 of 18

Last Updated: 09/26/2026