Amyotrophic lateral sclerosis with a heterozygous D91A SOD1 variant and classical ALS-TDP neuropathology
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical)
Reference7 articles.
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1. SOD1 gene screening in ALS – frequency of mutations, patients’ attitudes to genetic information and transition to tofersen treatment in a multi-center program;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2024-09-13
2. Tofersen decreases neurofilament levels supporting the pathogenesis of the SOD1 p.D91A variant in amyotrophic lateral sclerosis patients;Communications Medicine;2024-07-25
3. Clinical and patient‐reported outcomes and neurofilament response during tofersen treatment in SOD1‐related ALS—A multicenter observational study over 18 months;Muscle & Nerve;2024-06-20
4. Advancements and challenges in amyotrophic lateral sclerosis;Frontiers in Neuroscience;2024-05-22
5. Advantages of routine next‐generation sequencing over standard genetic testing in the amyotrophic lateral sclerosis clinic;European Journal of Neurology;2023-05-28
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