Reviews of spinal muscular atrophy in Taiwan
Spinal muscular atrophy (SMA) is one of the rare life-threatening hereditary autosomal recessive disorders. SMA is caused by the absence of a fully functional motor neuron protein gene that produces the survival motor neuron (SMN) protein. The SMN protein is encoded by two SMN genes: SMN1, which is...
Saved in:
Main Authors: | Yung-Hsiu Lu, Wei-Sheng Lin, Dau-Ming Niu, Ting-Rong Hsu |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2024-12-01
|
Series: | Tungs’ Medical Journal |
Subjects: | |
Online Access: | https://doi.org/10.4103/ETMJ.ETMJ-D-24-00033 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Comprehensive analysis of adverse events associated with onasemnogene abeparvovec (Zolgensma) in spinal muscular atrophy patients: insights from FAERS database
by: Wenwen Zhang, et al.
Published: (2025-01-01) -
Effect of nusinersen on pulmonary function in children with spinal muscular atrophy in the plateau region: A pilot study
by: Jicai Zhu, et al.
Published: (2025-01-01) -
Maximal mouth opening in infants and toddlers with spinal muscular atrophy: a prospective controlled study
by: Jana Zang, et al.
Published: (2025-01-01) -
Rare coexistence of spinal muscular atrophy with membranous nephropathy – A clinical conundrum with management dilemma
by: Gerry G. Mathew, et al.
Published: (2024-12-01) -
Safety and Efficacy of Nusinersen Focusing on Renal and Hematological Parameters in Spinal Muscular Atrophy
by: Hüseyin Bahadır Şenol, et al.
Published: (2025-01-01)