Xiushan Ge
Beijing, 100020, China
Last Updated: 09/26/2026
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Found 8 publications
Molecular Genetic Diagnosis of Spinal Muscular Atrophy: Clinical Utility, Challenges, and Lessons Learned from Illustrative Cases in a Single Center.
Journal: Genes
Published: July 01, 2026
Corrigendum: Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1-3.
Journal: Frontiers in neurology
Published: October 16, 2024
Clinical characteristics and genetics functional analysis of two children with Spinal muscular atrophy
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 30, 2024
Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1-3.
Journal: Frontiers in neurology
Published: February 15, 2024
Juvenile Generalized Myasthenia Gravis With AChR and MuSK Antibody Double Positivity: A Case Report With a Review of the Literature.
Journal: Frontiers in pediatrics
Published: October 02, 2021
Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model.
Journal: Human molecular genetics
Published: September 22, 2021
Factors associated with delayed diagnosis of spinal muscular atrophy in China and changes in diagnostic delay.
Journal: Neuromuscular disorders : NMD
Published: August 12, 2020
The natural history of infant spinal muscular atrophy in China: a study of 237 patients.
Journal: Journal of child neurology
Published: September 29, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026