Quantifying disease progression in amyotrophic lateral sclerosis

Author:

Simon Neil G.123,Turner Martin R.4,Vucic Steve35,Al‐Chalabi Ammar6,Shefner Jeremy7,Lomen‐Hoerth Catherine1,Kiernan Matthew C.8

Affiliation:

1. Department of NeurologyUniversity of CaliforniaSan Francisco San Francisco CA

2. Prince of Wales Clinical School, University of New South Wales Randwick Australia

3. Neuroscience Research AustraliaBarker StRandwick Australia

4. Nuffield Department of Clinical NeurosciencesUniversity of OxfordOxford United Kingdom

5. Westmead Clinical School, University of SydneySydney Australia

6. Department of Clinical NeuroscienceKing's College LondonLondon United Kingdom

7. Upstate Medical UniversitySyracuse NY

8. Brain and Mind Research Institute, University of SydneySydney Australia

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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1. Diffusion tensor imaging biomarkers and clinical assessments in amyotrophic lateral sclerosis (ALS) patients: an exploratory study;Annals of Medicine & Surgery;2024-07-23

2. Changes in saccadic intrusions over time as an objective biomarker to follow ALS disease progression;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2024-07-08

3. Methodological Quality of Clinical Trials in Amyotrophic Lateral Sclerosis: A Systematic Review;Journal of Neuromuscular Diseases;2024-07-02

4. Theme 10 - Disease Stratification and Phenotyping of Patients;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2023-11-06

5. Describing and characterising variability in ALS disease progression;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2023-10-05

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