Evaluation of the neurofilament light chain as a biomarker in children with spinal muscular atrophy treated with nusinersen
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health
Reference31 articles.
1. Neurofilament as a potential biomarker for spinal muscular atrophy;Darras;Ann Clin Transl Neurol,2019
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3. Spinal muscular atrophy: clinical classification and disease heterogeneity;Russman;J Child Neurol,2007
4. Nusinersen versus sham control in later-onset spinal muscular atrophy;Mercuri;N Engl J Med,2018
5. Nusinersen versus sham control in infantile-onset spinal muscular atrophy;Finkel;N Engl J Med,2017
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2. Serum myostatin as a candidate disease severity and progression biomarker of spinal muscular atrophy;Brain Communications;2024
3. Study on the efficacy, safety, and biomarkers of nusinersen in type II and III spinal muscular atrophy in children;Frontiers in Pediatrics;2023-12-04
4. Validation of remote collection and quantification of blood Neurofilament light in neurological diseases;2023-12-04
5. Cerebrospinal Fluid Proteomic Changes after Nusinersen in Patients with Spinal Muscular Atrophy;Journal of Clinical Medicine;2023-10-23
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