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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1969 1
1976 1
1977 1
1978 2
1979 2
1980 4
1981 9
1982 4
1983 5
1984 5
1985 7
1986 8
1987 11
1988 11
1989 21
1990 14
1991 33
1992 46
1993 46
1994 38
1995 48
1996 62
1997 84
1998 84
1999 95
2000 128
2001 114
2002 130
2003 161
2004 128
2005 147
2006 155
2007 188
2008 170
2009 162
2010 181
2011 174
2012 206
2013 223
2014 238
2015 293
2016 294
2017 311
2018 309
2019 345
2020 387
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2022 400
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2026 1

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6,332 results

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Page 1
Multiple system atrophy.
Fanciulli A, Stankovic I, Krismer F, Seppi K, Levin J, Wenning GK. Fanciulli A, et al. Int Rev Neurobiol. 2019;149:137-192. doi: 10.1016/bs.irn.2019.10.004. Epub 2019 Nov 21. Int Rev Neurobiol. 2019. PMID: 31779811 Review.
Multiple system atrophy (MSA) is a sporadic, adult-onset, relentlessly progressive neurodegenerative disorder, clinically characterized by various combinations of autonomic failure, parkinsonism and ataxia. ...
Multiple system atrophy (MSA) is a sporadic, adult-onset, relentlessly progressive neurodegenerative disorder, clinical …
Multiple-system atrophy.
Fanciulli A, Wenning GK. Fanciulli A, et al. N Engl J Med. 2015 Jan 15;372(3):249-63. doi: 10.1056/NEJMra1311488. N Engl J Med. 2015. PMID: 25587949 Review. No abstract available.
Inflammation in multiple system atrophy.
Leńska-Mieciek M, Madetko-Alster N, Alster P, Królicki L, Fiszer U, Koziorowski D. Leńska-Mieciek M, et al. Front Immunol. 2023 Jun 22;14:1214677. doi: 10.3389/fimmu.2023.1214677. eCollection 2023. Front Immunol. 2023. PMID: 37426656 Free PMC article. Review.
Multiple System Atrophy.
Claassen DO. Claassen DO. Continuum (Minneap Minn). 2022 Oct 1;28(5):1350-1363. doi: 10.1212/CON.0000000000001154. Continuum (Minneap Minn). 2022. PMID: 36222769 Review.
PURPOSE OF REVIEW: Patients with multiple system atrophy (MSA) can present with diverse clinical manifestations, and the clinical care required is complex and requires a thoughtful approach to emerging symptoms and treatment decisions. ...
PURPOSE OF REVIEW: Patients with multiple system atrophy (MSA) can present with diverse clinical manifestations, and th …
Multiple system atrophy: an update and emerging directions of biomarkers and clinical trials.
Liu M, Wang Z, Shang H. Liu M, et al. J Neurol. 2024 May;271(5):2324-2344. doi: 10.1007/s00415-024-12269-5. Epub 2024 Mar 14. J Neurol. 2024. PMID: 38483626 Free PMC article. Review.
Multiple system atrophy is a rare, debilitating, adult-onset neurodegenerative disorder that manifests clinically as a diverse combination of parkinsonism, cerebellar ataxia, and autonomic dysfunction. ...According to the updated Movement Disorder Society dia …
Multiple system atrophy is a rare, debilitating, adult-onset neurodegenerative disorder that manifests clinically as a …
Multiple System Atrophy.
Xie T. Xie T. Continuum (Minneap Minn). 2025 Aug;31(4):1000-1022. doi: 10.1212/cont.0000000000001598. Epub 2025 Aug 1. Continuum (Minneap Minn). 2025. PMID: 40748131 Review.
The 2022 International Parkinson and Movement Disorder Society criteria enable an accurate and early diagnosis of clinically established multiple system atrophy, clinically probable multiple system atrophy, prodromal possible multiple …
The 2022 International Parkinson and Movement Disorder Society criteria enable an accurate and early diagnosis of clinically established …
Multiple system atrophy: at the crossroads of cellular, molecular and genetic mechanisms.
Stefanova N, Wenning GK. Stefanova N, et al. Nat Rev Neurosci. 2023 Jun;24(6):334-346. doi: 10.1038/s41583-023-00697-7. Epub 2023 Apr 21. Nat Rev Neurosci. 2023. PMID: 37085728 Review.
Multiple system atrophy (MSA) is a rare oligodendroglial alpha-synucleinopathy characterized by neurodegeneration in striatonigral and olivopontocerebellar regions and autonomic brain centres. ...
Multiple system atrophy (MSA) is a rare oligodendroglial alpha-synucleinopathy characterized by neurodegeneration in st …
Multiple system atrophy.
Wenning GK, Krismer F. Wenning GK, et al. Handb Clin Neurol. 2013;117:229-41. doi: 10.1016/B978-0-444-53491-0.00019-5. Handb Clin Neurol. 2013. PMID: 24095129 Review.
Multiple system atrophy (MSA) is a sporadic and fatal alpha-synuclein-linked oligodendrogliopathy manifesting with progressive autonomic failure, poorly levodopa-responsive parkinsonism, and cerebellar ataxia, in any combination. ...
Multiple system atrophy (MSA) is a sporadic and fatal alpha-synuclein-linked oligodendrogliopathy manifesting with prog …
Multiple System Atrophy: An Oligodendroglioneural Synucleinopathy1.
Jellinger KA. Jellinger KA. J Alzheimers Dis. 2018;62(3):1141-1179. doi: 10.3233/JAD-170397. J Alzheimers Dis. 2018. PMID: 28984582 Free PMC article. Review.
Multiple system atrophy (MSA) is an orphan, fatal, adult-onset neurodegenerative disorder of uncertain etiology that is clinically characterized by various combinations of parkinsonism, cerebellar, autonomic, and motor dysfunction. ...
Multiple system atrophy (MSA) is an orphan, fatal, adult-onset neurodegenerative disorder of uncertain etiology that is …
Multiple system atrophy.
Kaufmann H. Kaufmann H. Curr Opin Neurol. 1998 Aug;11(4):351-5. doi: 10.1097/00019052-199808000-00011. Curr Opin Neurol. 1998. PMID: 9725081 Review.
Although the precise definition of multiple system atrophy has been difficult, a recent consensus in diagnostic criteria for multiple system atrophy has been achieved. This should lead to progress in defining the underlying pathophysiolog …
Although the precise definition of multiple system atrophy has been difficult, a recent consensus in diagnostic criteri …
6,332 results