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The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration
Sarah Opie-Martin, Alfredo Iacoangeli, Simon D. Topp, Olubunmi Abel, Keith Mayl, Puja R. Mehta, Aleksey Shatunov, Isabella Fogh, Harry Bowles, Naomi Limbachiya, Thomas P. Spargo, Ahmad Al-Khleifat, Kelly L. Williams, Jennifer Jockel-Balsarotti, Taha Bali, Wade Self, Lyndal Henden, Garth A. Nicholson, Nicola Ticozzi, Diane McKenna-Yasek
*Corresponding author for this work
- King's College London
- Department of Psychology and Neuroscience
- SLaM South London and Maudsley NHS Foundation Trust
- Homerton University Hospital NHS Foundation Trust
- Macquarie University
- Washington University School of Medicine in St. Louis
- Concord Repatriation General Hospital
- IRCCS Istituto Auxologico Italiano
- Policlinico of Milan
- University of Massachusetts Medical School
- Peking University Third Hospital
- Section of Infection, Inflammation and Immunity, University of Sheffield School of Medicine and Biomedical Sciences, L Floor, Royal Hallamshire Hospital, Glossop Road, Sheffield, UK.
- University of Turin
- AOU Città della Salute e della Scienza di Torino
- Ulm University Medical Centre
- Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
- University of Ulm
- Heidelberg University
- Emory University School of Medicine
- Hospital San Rafael
- University Hospitals Leuven
- KU Leuven
- Department of Urology
- UMC University Medical Center Utrecht
- Centre de Référence pour la SLA et les Autres Maladies du Motoneurone (FILSLAN)
- Centre de Compétences Neuropathies Amyloïdes Familiales et Autres Neuropathies Périphériques Rares (NNERF)
- University of Belgrade
- Northwestern University
- University Hospital Gui de Chauliac
- Koç University
- University of Auckland
Research output: Contribution to journal › Article › peer-review
20
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(Scopus)