Xiuxia Wang

Shijiazhuang, 050000, China

Last Updated: 09/26/2026

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Found 13 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

Randomized, Double-Blind, Placebo-Controlled Trial on the Efficacy, Safety and Tolerability of Modified-Release Methylphenidate (MPH-MR) in Chinese Children and Adolescents with Attention-Deficit/Hyperactivity Disorder (ADHD).

Randomized, Double-Blind, Placebo-Controlled Trial on the Efficacy, Safety and Tolerability of Modified-Release Methylphenidate (MPH-MR) in Chinese Children and Adolescents with Attention-Deficit/Hyperactivity Disorder (ADHD).

Journal: CNS drugs

Published: November 03, 2024

Efficacy of Clonidine Adhesive Patch for Patients With Tourette Syndrome: A Randomized, Double-blind, Placebo-Controlled, Multicenter Clinical Trial.

Efficacy of Clonidine Adhesive Patch for Patients With Tourette Syndrome: A Randomized, Double-blind, Placebo-Controlled, Multicenter Clinical Trial.

Journal: Clinical neuropharmacology

Published: September 11, 2024

Administration practices of and adherence to nusinersen in children with spinal muscular atrophy: a multicenter disease registry study in China.

Administration practices of and adherence to nusinersen in children with spinal muscular atrophy: a multicenter disease registry study in China.

Journal: BMC pediatrics

Published: March 29, 2024

Nusinersen effectiveness and safety in pediatric patients with 5q-spinal muscular atrophy: a multi-center disease registry in China.

Nusinersen effectiveness and safety in pediatric patients with 5q-spinal muscular atrophy: a multi-center disease registry in China.

Journal: Journal of neurology

Published: February 21, 2024

Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay.

Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay.

Journal: Molecular psychiatry

Published: January 13, 2024

Clinical and functional study of two de novo variations of CDKL5 gene.

Clinical and functional study of two de novo variations of CDKL5 gene.

Journal: Neurogenetics

Published: March 30, 2023

ATP6V0C gene variants were identified in individuals with epilepsy, with or without developmental delay.

ATP6V0C gene variants were identified in individuals with epilepsy, with or without developmental delay.

Journal: Journal of human genetics

Published: November 07, 2022

A homozygous variant of WDR45B results in global developmental delay: Additional case and literature review.

A homozygous variant of WDR45B results in global developmental delay: Additional case and literature review.

Journal: Molecular genetics & genomic medicine

Published: February 22, 2022

Ketogenic Diet in Infants with Early-Onset Epileptic Encephalopathy and SCN2A Mutation.

Ketogenic Diet in Infants with Early-Onset Epileptic Encephalopathy and SCN2A Mutation.

Journal: Yonsei medical journal

Published: August 12, 2020

Analysis of SCN4A gene variation in a Chinese pedigree affected with skeletal muscle sodium channelopathies

Analysis of SCN4A gene variation in a Chinese pedigree affected with skeletal muscle sodium channelopathies

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

Published: August 11, 2019

Neuroprotective effect of astaxanthin on newborn rats exposed to prenatal maternal seizures.

Neuroprotective effect of astaxanthin on newborn rats exposed to prenatal maternal seizures.

Journal: Brain research bulletin

Published: April 21, 2018

Showing 1-12 of 13

Last Updated: 09/26/2026