Multiple System Atrophy Without Dysautonomia

The MDS-MSA criteria expand the diagnostic scope by identifying a motor-only subgroup with a distinct and potentially slower disease course. These findings underscore the importance of including motor-only patients in natural history and interventional studies. Limitations include retrospective data collection and potential variability in symptom documentation.

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Publication Details

Journal
Neurology
Published
2025-11-13
DOI
https://doi.org/10.1212/wnl.0000000000214316
Citations
1
Primary Topic
Hereditary Neurological Disorders
Type
article
Field-Weighted Citation Impact
0.91

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article

Multiple System Atrophy Without Dysautonomia

Anthony E. Lang, Ida Jensen, Laura Molina‐Porcel, John Cornelis Van Swieten et al.
1 citations
Neurology
Hereditary Neurological Disorders
0.91
article

Multiple System Atrophy Without Dysautonomia

Anthony E. Lang, Ida Jensen, Laura Molina‐Porcel, John Cornelis Van Swieten, Elise G.P. Dopper, Alexander Bernhardt, Gábor G. Kovács, Annemieke J.M. Rozemüller, Christer Nilsson, Sarah Bebermeier, Joseph Seemiller, Franziska Hopfner, Claire Troakes, Johannes Levin, S Berger, Alexander Pantelyat, Johanne Heine, Nathaniel Bendahan, Sabrina Katzdobler, Edward B. Lee, Elisabet Englund, Günter U. Höglinger, Jochen Herms, Jesse Cohen, Mojtaba Nemati, Viktoria Ruf, Yaroslau Compta, David J. Irwin, Albert Vamanu, S Downes
article en
1 citations

Abstract

The MDS-MSA criteria expand the diagnostic scope by identifying a motor-only subgroup with a distinct and potentially slower disease course. These findings underscore the importance of including motor-only patients in natural history and interventional studies. Limitations include retrospective data collection and potential variability in symptom documentation.

NeurologyVol. 105(11)
Leibniz University Hannover (DE), Pennsylvania State University (US), University Health Network (CA), Johns Hopkins University (US), King's College London (GB), Lund University (SE), Toronto Western Hospital (CA), Johns Hopkins Medicine (US), German Center for Neurodegenerative Diseases (DE), Erasmus MC (NL), LMU Klinikum (DE), University of Florida (US), Medizinische Hochschule Hannover (DE), Jacksonville University (US), Amsterdam Neuroscience (NL), Occupational Cancer Research Centre (CA), Institute for Neurodegenerative Disorders (US), Munich Cluster for Systems Neurology (DE), Hospital Clínic de Barcelona (ES), L3S Research Center (DE), Institute on Aging (US), Ontario Brain Institute (CA), University of Pennsylvania (US), Ludwig-Maximilians-Universität München (DE), Penn State Milton S. Hershey Medical Center (US), Erasmus University Rotterdam (NL)
Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, Biogen, Teva Pharmaceutical Industries, University of Pennsylvania, Fondation Brain Canada, Demensförbundet, Edmond J. Safra Philanthropic Foundation, Ludwig-Maximilians-Universität München, Parkinson Canada, National Institutes of Health, Parkinsonfonden, Bayer Vital, Canadian Institutes of Health Research
Openalex Percentile: Top 20%
Hereditary Neurological Disorders
0.91
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