Spinal Muscular Atrophy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics(clinical),Clinical Neurology
Reference55 articles.
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3. Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72,400 specimens;Eur J Hum Genet,2012
4. Zwei frühinfantile hereditäre fälle von progressiver muskelatrophie unter dem bilde der dystrophie, aber anf neurotischer grundlage;Archiv für Psychiatrie und Nervenkrankheiten,1891
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1. A Five-Year Review of Newborn Screening for Spinal Muscular Atrophy in the State of Utah: Lessons Learned;International Journal of Neonatal Screening;2024-07-22
2. Metabolic syndrome is common in adults with 5q‐spinal muscular atrophy and impacts quality of life and fatigue;Muscle & Nerve;2024-06-14
3. The dynamic of changes of pNFH levels in the CSF compared with the motor scales’ scores during three years of nusinersen treatment in children with spinal muscular atrophy types 2 and 3;Balneo and PRM Research Journal;2024-03-31
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5. Spinal Muscular Atrophy With Severe Hyperlordosis: A Case Report;Cureus;2024-02-09
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