Multiple system atrophy (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Multiple system atrophy" in English language version.

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82nih.gov

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businessinsider.com

"Kerry Simon, Las Vegas 'Iron Chef' winner, dies at 60". Business Insider. Archived from the original on 14 November 2018. Retrieved 14 November 2018.

doi.org

Peng C, Gathagan RJ, Covell DJ, Medellin C, Stieber A, Robinson JL, et al. (May 2018). "Cellular milieu imparts distinct pathological α-synuclein strains in α-synucleinopathies". Nature. 557 (7706): 558–563. Bibcode:2018Natur.557..558P. doi:10.1038/s41586-018-0104-4. PMC 5970994. PMID 29743672.{{cite journal}}: CS1 maint: overridden setting (link)
Fanciulli A, Wenning GK (January 2015). "Multiple-system atrophy". The New England Journal of Medicine. 372 (3): 249–263. doi:10.1056/NEJMra1311488. PMID 25587949.
Swan L, Dupont J (May 1999). "Multiple system atrophy". Physical Therapy. 79 (5): 488–494. doi:10.1093/ptj/79.5.488. PMID 10331752.
^{[unreliable medical source?]}Sikorska B, Papierz W, Preusser M, Liberski PP, Budka H (February 2007). "Synucleinopathy with features of both multiple system atrophy and dementia with Lewy bodies". Neuropathology and Applied Neurobiology. 33 (1): 126–129. doi:10.1111/j.1365-2990.2006.00817.x. PMID 17239015. S2CID 40186391.
Aoki N, Boyer PJ, Lund C, Lin WL, Koga S, Ross OA, et al. (July 2015). "Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein". Acta Neuropathologica. 130 (1): 93–105. doi:10.1007/s00401-015-1442-z. PMC 6764097. PMID 25962793.{{cite journal}}: CS1 maint: overridden setting (link)
Bensimon G, Ludolph A, Agid Y, Vidailhet M, Payan C, Leigh PN (January 2009). "Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study". Brain. 132 (Pt 1): 156–171. doi:10.1093/brain/awn291. PMC 2638696. PMID 19029129.
Oertel WH, Wächter T, Quinn NP, Ulm G, Brandstädter D (April 2003). "Reduced genital sensitivity in female patients with multiple system atrophy of parkinsonian type". Movement Disorders. 18 (4): 430–432. doi:10.1002/mds.10384. PMID 12671951. S2CID 28102026.
Stępnicki (20 August 2018). "Current Concepts and Treatments of Schizophrenia". Molecules. 23 (8): 2087. doi:10.3390/molecules23082087. ISSN 1420-3049. PMC 6222385. PMID 30127324.
Ogawa T, Fujii S, Kuya K, Kitao SI, Shinohara Y, Ishibashi M, et al. (September 2018). "Role of Neuroimaging on Differentiation of Parkinson's Disease and Its Related Diseases". Yonago Acta Medica (Review). 61 (3): 145–155. doi:10.33160/yam.2018.09.001. PMC 6158357. PMID 30275744. Parkinsonian syndromes are a group of movement disorders characterized by classical motor symptoms such as tremors, bradykinesia, and rigidity. They are most frequently due to primary neurodegenerative disease, resulting in the loss of dopaminergic nerve terminals along the nigrostriatal pathway, similar to idiopathic PD, MSA, PSP, CBD, and DLB.
Hodos W (2009). "Evolution of Cerebellum". Encyclopedia of Neuroscience. Springer. pp. 1240–1243. doi:10.1007/978-3-540-29678-2_3124. ISBN 978-3-540-23735-8.
Richard C, Amarenco G, Palma JA, Kaufmann H, Drapier S, Gamé X, et al. (2019). "Early bladder dysfunction in multiple system atrophy: who seek shall find". Clin Auton Res. 29 (6): 625–6. doi:10.1007/s10286-019-00648-2. PMID 1705345.
Sakakibara R, Panicker J, Finazzi-Agro E, Iacovelli V, Bruschini H, Subcomittee PD, et al. (2016). "A guideline for the management of bladder dysfunction in Parkinson's disease and other gait disorders". Neurourol Urodyn. 35 (5): 551–63. doi:10.1002/nau.22764. PMID 25810035.
Gilman S, Koeppe RA, Chervin RD, Consens FB, Little R, An H, et al. (July 2003). "REM sleep behavior disorder is related to striatal monoaminergic deficit in MSA". Neurology. 61 (1): 29–34. doi:10.1212/01.wnl.0000073745.68744.94. PMID 12847152. S2CID 9538306.{{cite journal}}: CS1 maint: overridden setting (link)
Brown RG, Lacomblez L, Landwehrmeyer BG, Bak T, Uttner I, Dubois B, et al. (August 2010). "Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy". Brain. 133 (Pt 8): 2382–2393. doi:10.1093/brain/awq158. PMID 20576697.{{cite journal}}: CS1 maint: overridden setting (link)
Sasaki H, Emi M, Iijima H, Ito N, Sato H, Yabe I, et al. (June 2011). "Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy". Molecular Brain. 4: 24. doi:10.1186/1756-6606-4-24. PMC 3141657. PMID 21658278. Copy number loss of SHC2 strongly indicates a causal link to MSA.{{cite journal}}: CS1 maint: overridden setting (link)
Ferguson MC, Garland EM, Hedges L, Womack-Nunley B, Hamid R, Phillips JA, et al. (February 2014). "SHC2 gene copy number in multiple system atrophy (MSA)". Clinical Autonomic Research. 24 (1): 25–30. doi:10.1007/s10286-013-0216-8. PMC 3946192. PMID 24170347.{{cite journal}}: CS1 maint: overridden setting (link)
Sullivan R, Yau WY, Chelban V, Rossi S, O'Connor E, Wood NW, et al. (July 2020). "RFC1 Intronic Repeat Expansions Absent in Pathologically Confirmed Multiple Systems Atrophy". Movement Disorders. 35 (7): 1277–1279. doi:10.1002/mds.28074. PMID 32333430. S2CID 216129457.{{cite journal}}: CS1 maint: overridden setting (link)
Cortese A, Simone R, Sullivan R, Vandrovcova J, Tariq H, Yau WY, et al. (April 2019). "Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia". Nature Genetics. 51 (4): 649–658. doi:10.1038/s41588-019-0372-4. PMC 6709527. PMID 30926972.{{cite journal}}: CS1 maint: overridden setting (link)
Wenning GK, Colosimo C, Geser F, Poewe W (February 2004). "Multiple system atrophy". The Lancet. Neurology. 3 (2): 93–103. doi:10.1016/S1474-4422(03)00662-8. PMID 14747001. S2CID 10162139.
Wenning GK, Colosimo C, Geser F, Poewe W (March 2004). "Erratum". Lancet Neurol. 3 (3): 137. doi:10.1016/S1474-4422(04)00695-7. S2CID 208782339.
Jellinger KA, Lantos PL (June 2010). "Papp-Lantos inclusions and the pathogenesis of multiple system atrophy: an update". Acta Neuropathologica. 119 (6): 657–667. doi:10.1007/s00401-010-0672-3. PMID 20309568. S2CID 19759468.
Arima K, Uéda K, Sunohara N, Arakawa K, Hirai S, Nakamura M, et al. (November 1998). "NACP/alpha-synuclein immunoreactivity in fibrillary components of neuronal and oligodendroglial cytoplasmic inclusions in the pontine nuclei in multiple system atrophy". Acta Neuropathologica. 96 (5): 439–444. doi:10.1007/s004010050917. PMID 9829806. S2CID 10804119.{{cite journal}}: CS1 maint: overridden setting (link)
Al-Chalabi A, Dürr A, Wood NW, Parkinson MH, Camuzat A, Hulot JS, et al. (September 2009). "Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy". PLOS ONE. 4 (9): e7114. Bibcode:2009PLoSO...4.7114A. doi:10.1371/journal.pone.0007114. PMC 2743996. PMID 19771175.{{cite journal}}: CS1 maint: overridden setting (link)
Stefanova N, Wenning GK (February 2016). "Review: Multiple system atrophy: emerging targets for interventional therapies". Neuropathology and Applied Neurobiology. 42 (1): 20–32. doi:10.1111/nan.12304. PMC 4788141. PMID 26785838.
De Nuccio F, Kashyrina M, Serinelli F, Laferrière F, Lofrumento DD, De Giorgi F, et al. (February 2023). "Oligodendrocytes Prune Axons Containing α-Synuclein Aggregates In Vivo: Lewy Neurites as Precursors of Glial Cytoplasmic Inclusions in Multiple System Atrophy?". Biomolecules. 13 (2): 269. doi:10.3390/biom13020269. PMC 9953613. PMID 36830639.
Piao YS, Hayashi S, Hasegawa M, Wakabayashi K, Yamada M, Yoshimoto M, et al. (March 2001). "Co-localization of alpha-synuclein and phosphorylated tau in neuronal and glial cytoplasmic inclusions in a patient with multiple system atrophy of long duration". Acta Neuropathologica. 101 (3): 285–293. doi:10.1007/s004010000292. PMID 11307630. S2CID 25650403.{{cite journal}}: CS1 maint: overridden setting (link)
Gilman S, Low PA, Quinn N, Albanese A, Ben-Shlomo Y, Fowler CJ, et al. (February 1999). "Consensus statement on the diagnosis of multiple system atrophy". Journal of the Neurological Sciences. 163 (1): 94–98. doi:10.1016/s0022-510x(98)00304-9. hdl:2027.42/41757. PMID 10223419. S2CID 13307970.{{cite journal}}: CS1 maint: overridden setting (link)
Gilman S, Wenning GK, Low PA, Brooks DJ, Mathias CJ, Trojanowski JQ, et al. (August 2008). "Second consensus statement on the diagnosis of multiple system atrophy". Neurology. 71 (9): 670–676. doi:10.1212/01.wnl.0000324625.00404.15. PMC 2676993. PMID 18725592.{{cite journal}}: CS1 maint: overridden setting (link)
Wenning GK, Stankovic I, Vignatelli L, Fanciulli A, Calandra-Buonaura G, Seppi K, et al. (2022). "The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy". Movement Disorders. 37 (6): 1131–48. doi:10.1002/mds.29005. hdl:11585/899814. PMC 9321158. PMID 35445419.
Koga S, Aoki N, Uitti RJ, van Gerpen JA, Cheshire WP, Josephs KA, et al. (August 2015). "When DLB, PD, and PSP masquerade as MSA: an autopsy study of 134 patients". Neurology. 85 (5): 404–412. doi:10.1212/WNL.0000000000001807. PMC 4534078. PMID 26138942.{{cite journal}}: CS1 maint: overridden setting (link)
Landers M, Adams M, Acosta K, Fox A. (2009). "Challenge-oriented gait and balance training in sporadic olivopontocerebellar atrophy: a case study". J Neurol Phys Ther. 33 (3): 160–168. doi:10.1097/npt.0b013e3181b511f4. PMID 19809395. S2CID 24642594.
Berciano J, Boesch S, Pérez-Ramos JM, Wenning GK (2006). "Olivopontocerebellar atrophy: toward a better nosological definition". Mov. Disord. 21 (10): 1607–13. doi:10.1002/mds.21052. PMID 16874757. S2CID 38376147.
Papp MI, Kahn JE, Lantos PL (December 1989). "Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)". Journal of the Neurological Sciences. 94 (1–3): 79–100. doi:10.1016/0022-510X(89)90219-0. PMID 2559165. S2CID 1199951.
Waxman EA, Giasson BI (July 2009). "Molecular mechanisms of alpha-synuclein neurodegeneration". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1792 (7): 616–624. doi:10.1016/j.bbadis.2008.09.013. PMC 2756732. PMID 18955133.
Ozawa T, Paviour D, Quinn NP, Josephs KA, Sangha H, Kilford L, et al. (December 2004). "The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations". Brain. 127 (Pt 12): 2657–2671. doi:10.1093/brain/awh303. PMID 15509623.{{cite journal}}: CS1 maint: overridden setting (link)
Brettschneider J, Suh E, Robinson JL, Fang L, Lee EB, Irwin DJ, et al. (November 2018). "Converging Patterns of α-Synuclein Pathology in Multiple System Atrophy". Journal of Neuropathology and Experimental Neurology. 77 (11): 1005–1016. doi:10.1093/jnen/nly080. PMC 6181179. PMID 30203094.{{cite journal}}: CS1 maint: overridden setting (link)
Hass EW, Sorrentino ZA, Lloyd GM, McFarland NR, Prokop S, Giasson BI (May 2021). "Robust α-synuclein pathology in select brainstem neuronal populations is a potential instigator of multiple system atrophy". Acta Neuropathologica Communications. 9 (1): 80. doi:10.1186/s40478-021-01173-y. PMC 8091528. PMID 33941284.
Hass EW, Sorrentino ZA, Xia Y, Lloyd GM, Trojanowski JQ, Prokop S, et al. (August 2021). "Disease-, region- and cell type specific diversity of α-synuclein carboxy terminal truncations in synucleinopathies". Acta Neuropathologica Communications. 9 (1): 146. doi:10.1186/s40478-021-01242-2. PMC 8403399. PMID 34454615.
Dhillon JS, Trejo-Lopez JA, Riffe C, McFarland NR, Hiser WM, Giasson BI, et al. (July 2019). "Dissecting α-synuclein inclusion pathology diversity in multiple system atrophy: implications for the prion-like transmission hypothesis". Laboratory Investigation; A Journal of Technical Methods and Pathology. 99 (7): 982–992. doi:10.1038/s41374-019-0198-9. PMC 7209695. PMID 30737468.
Shahnawaz M, Mukherjee A, Pritzkow S, Mendez N, Rabadia P, Liu X, et al. (February 2020). "Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy". Nature. 578 (7794): 273–277. Bibcode:2020Natur.578..273S. doi:10.1038/s41586-020-1984-7. PMC 7066875. PMID 32025029.{{cite journal}}: CS1 maint: overridden setting (link)
Goedert M, Jakes R, Spillantini MG (2017). "The Synucleinopathies: Twenty Years On". Journal of Parkinson's Disease (Review). 7 (s1): S51 – S69. doi:10.3233/JPD-179005. PMC 5345650. PMID 28282814.
The Consensus Committee of the American Autonomic Society and the American Academy of Neurology (May 1996). "Consensus statement on the definition of orthostatic hypotension, pure autonomic failure, and multiple system atrophy". Neurology. 46 (5): 1470. doi:10.1212/wnl.46.5.1470. PMID 8628505. S2CID 219212717.
Ahmed Z, Asi YT, Sailer A, Lees AJ, Houlden H, Revesz T, et al. (February 2012). "The neuropathology, pathophysiology and genetics of multiple system atrophy". Neuropathology and Applied Neurobiology. 38 (1): 4–24. doi:10.1111/j.1365-2990.2011.01234.x. PMID 22074330. S2CID 22901422.
Shy GM, Drager GA (May 1960). "A neurological syndrome associated with orthostatic hypotension: a clinical-pathologic study". Archives of Neurology. 2 (5): 511–527. doi:10.1001/archneur.1960.03840110025004. PMID 14446364.
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Calandra-Buonaura G, Doria A, Lopane G, Guaraldi P, Capellari S, Martinelli P, et al. (February 2016). "Pharmacodynamics of a low subacute levodopa dose helps distinguish between multiple system atrophy with predominant Parkinsonism and Parkinson's disease". Journal of Neurology. 263 (2): 250–256. doi:10.1007/s00415-015-7961-7. PMID 26566913. S2CID 189866517.{{cite journal}}: CS1 maint: overridden setting (link)
Hardy J (2008). "Multiple system atrophy: pathophysiology, treatment and nursing care". Nursing Standard. 22 (22): 50–6, quiz 58. doi:10.7748/ns2008.02.22.22.50.c6359. PMID 18333558.
Palma JA, Kaufmann H (February 2020). "Management of Orthostatic Hypotension". Continuum. 26 (1): 154–177. doi:10.1212/CON.0000000000000816. PMC 7339914. PMID 31996627.
Palma JA, Redel-Traub G, Porciuncula A, Samaniego-Toro D, Millar Vernetti P, Lui YW, et al. (June 2020). "The impact of supine hypertension on target organ damage and survival in patients with synucleinopathies and neurogenic orthostatic hypotension". Parkinsonism & Related Disorders. 75 (75): 97–104. doi:10.1016/j.parkreldis.2020.04.011. PMC 7415666. PMID 32516630.
Papapetropoulos S, Tuchman A, Laufer D, Papatsoris AG, Papapetropoulos N, Mash DC (March 2007). "Causes of death in multiple system atrophy". Journal of Neurology, Neurosurgery, and Psychiatry. 78 (3): 327–329. doi:10.1136/jnnp.2006.103929. PMC 2117630. PMID 17308296.
Lee PH, Lee JE, Kim HS, Song SK, Lee HS, Nam HS, et al. (July 2012). "A randomized trial of mesenchymal stem cells in multiple system atrophy". Annals of Neurology. 72 (1): 32–40. doi:10.1002/ana.23612. PMID 22829267. S2CID 5201446.{{cite journal}}: CS1 maint: overridden setting (link)

handle.net

hdl.handle.net

Gilman S, Low PA, Quinn N, Albanese A, Ben-Shlomo Y, Fowler CJ, et al. (February 1999). "Consensus statement on the diagnosis of multiple system atrophy". Journal of the Neurological Sciences. 163 (1): 94–98. doi:10.1016/s0022-510x(98)00304-9. hdl:2027.42/41757. PMID 10223419. S2CID 13307970.{{cite journal}}: CS1 maint: overridden setting (link)
Wenning GK, Stankovic I, Vignatelli L, Fanciulli A, Calandra-Buonaura G, Seppi K, et al. (2022). "The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy". Movement Disorders. 37 (6): 1131–48. doi:10.1002/mds.29005. hdl:11585/899814. PMC 9321158. PMID 35445419.

harvard.edu

ui.adsabs.harvard.edu

Peng C, Gathagan RJ, Covell DJ, Medellin C, Stieber A, Robinson JL, et al. (May 2018). "Cellular milieu imparts distinct pathological α-synuclein strains in α-synucleinopathies". Nature. 557 (7706): 558–563. Bibcode:2018Natur.557..558P. doi:10.1038/s41586-018-0104-4. PMC 5970994. PMID 29743672.{{cite journal}}: CS1 maint: overridden setting (link)
Al-Chalabi A, Dürr A, Wood NW, Parkinson MH, Camuzat A, Hulot JS, et al. (September 2009). "Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy". PLOS ONE. 4 (9): e7114. Bibcode:2009PLoSO...4.7114A. doi:10.1371/journal.pone.0007114. PMC 2743996. PMID 19771175.{{cite journal}}: CS1 maint: overridden setting (link)
Shahnawaz M, Mukherjee A, Pritzkow S, Mendez N, Rabadia P, Liu X, et al. (February 2020). "Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy". Nature. 578 (7794): 273–277. Bibcode:2020Natur.578..273S. doi:10.1038/s41586-020-1984-7. PMC 7066875. PMID 32025029.{{cite journal}}: CS1 maint: overridden setting (link)

house.gov

Cummings E (30 September 2000). "Standing up for justice". Baltimore AFRO-American. Archived from the original on 4 May 2008. Retrieved 10 December 2018.

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Turner A. "Olympic Legend Andrianov Dies at 58". International Gymnast Magazine Online. Retrieved 10 December 2018.

lecturio.com

"Hypotension". The Lecturio Medical Concept Library. Retrieved 27 July 2021.
"Constipation". The Lecturio Medical Concept Library. Retrieved 27 July 2021.

legacy.com

"Ronald Green Obituary". The Miami Herald. 26 July 2012.

mayoclinic.org

Multiple system atrophy (MSA) mayoclinic.org, accessed 20 May 2018

medlineplus.gov

"Multiple system atrophy – cerebellar subtype: MedlinePlus Medical Encyclopedia". medlineplus.gov. Retrieved 24 May 2019.

medscape.com

emedicine.medscape.com

"Multiple System Atrophy Clinical Presentation". Retrieved 7 January 2018.
Bloomfield SM, Hanna PA, Noor ER, Dalvi AI (24 September 2018). Benbadis SR (ed.). "multiple system atrophy overview". Medscape. WebMD LLC.

nih.gov

pubmed.ncbi.nlm.nih.gov

Peng C, Gathagan RJ, Covell DJ, Medellin C, Stieber A, Robinson JL, et al. (May 2018). "Cellular milieu imparts distinct pathological α-synuclein strains in α-synucleinopathies". Nature. 557 (7706): 558–563. Bibcode:2018Natur.557..558P. doi:10.1038/s41586-018-0104-4. PMC 5970994. PMID 29743672.{{cite journal}}: CS1 maint: overridden setting (link)
Fanciulli A, Wenning GK (January 2015). "Multiple-system atrophy". The New England Journal of Medicine. 372 (3): 249–263. doi:10.1056/NEJMra1311488. PMID 25587949.
Swan L, Dupont J (May 1999). "Multiple system atrophy". Physical Therapy. 79 (5): 488–494. doi:10.1093/ptj/79.5.488. PMID 10331752.
Burn DJ, Jaros E (December 2001). "Multiple system atrophy: cellular and molecular pathology". Molecular Pathology. 54 (6): 419–426. PMC 1187133. PMID 11724918.
^{[unreliable medical source?]}Sikorska B, Papierz W, Preusser M, Liberski PP, Budka H (February 2007). "Synucleinopathy with features of both multiple system atrophy and dementia with Lewy bodies". Neuropathology and Applied Neurobiology. 33 (1): 126–129. doi:10.1111/j.1365-2990.2006.00817.x. PMID 17239015. S2CID 40186391.
Aoki N, Boyer PJ, Lund C, Lin WL, Koga S, Ross OA, et al. (July 2015). "Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein". Acta Neuropathologica. 130 (1): 93–105. doi:10.1007/s00401-015-1442-z. PMC 6764097. PMID 25962793.{{cite journal}}: CS1 maint: overridden setting (link)
Bensimon G, Ludolph A, Agid Y, Vidailhet M, Payan C, Leigh PN (January 2009). "Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study". Brain. 132 (Pt 1): 156–171. doi:10.1093/brain/awn291. PMC 2638696. PMID 19029129.
Oertel WH, Wächter T, Quinn NP, Ulm G, Brandstädter D (April 2003). "Reduced genital sensitivity in female patients with multiple system atrophy of parkinsonian type". Movement Disorders. 18 (4): 430–432. doi:10.1002/mds.10384. PMID 12671951. S2CID 28102026.
Stępnicki (20 August 2018). "Current Concepts and Treatments of Schizophrenia". Molecules. 23 (8): 2087. doi:10.3390/molecules23082087. ISSN 1420-3049. PMC 6222385. PMID 30127324.
Ogawa T, Fujii S, Kuya K, Kitao SI, Shinohara Y, Ishibashi M, et al. (September 2018). "Role of Neuroimaging on Differentiation of Parkinson's Disease and Its Related Diseases". Yonago Acta Medica (Review). 61 (3): 145–155. doi:10.33160/yam.2018.09.001. PMC 6158357. PMID 30275744. Parkinsonian syndromes are a group of movement disorders characterized by classical motor symptoms such as tremors, bradykinesia, and rigidity. They are most frequently due to primary neurodegenerative disease, resulting in the loss of dopaminergic nerve terminals along the nigrostriatal pathway, similar to idiopathic PD, MSA, PSP, CBD, and DLB.
Richard C, Amarenco G, Palma JA, Kaufmann H, Drapier S, Gamé X, et al. (2019). "Early bladder dysfunction in multiple system atrophy: who seek shall find". Clin Auton Res. 29 (6): 625–6. doi:10.1007/s10286-019-00648-2. PMID 1705345.
Sakakibara R, Panicker J, Finazzi-Agro E, Iacovelli V, Bruschini H, Subcomittee PD, et al. (2016). "A guideline for the management of bladder dysfunction in Parkinson's disease and other gait disorders". Neurourol Urodyn. 35 (5): 551–63. doi:10.1002/nau.22764. PMID 25810035.
Gilman S, Koeppe RA, Chervin RD, Consens FB, Little R, An H, et al. (July 2003). "REM sleep behavior disorder is related to striatal monoaminergic deficit in MSA". Neurology. 61 (1): 29–34. doi:10.1212/01.wnl.0000073745.68744.94. PMID 12847152. S2CID 9538306.{{cite journal}}: CS1 maint: overridden setting (link)
Brown RG, Lacomblez L, Landwehrmeyer BG, Bak T, Uttner I, Dubois B, et al. (August 2010). "Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy". Brain. 133 (Pt 8): 2382–2393. doi:10.1093/brain/awq158. PMID 20576697.{{cite journal}}: CS1 maint: overridden setting (link)
Sasaki H, Emi M, Iijima H, Ito N, Sato H, Yabe I, et al. (June 2011). "Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy". Molecular Brain. 4: 24. doi:10.1186/1756-6606-4-24. PMC 3141657. PMID 21658278. Copy number loss of SHC2 strongly indicates a causal link to MSA.{{cite journal}}: CS1 maint: overridden setting (link)
Ferguson MC, Garland EM, Hedges L, Womack-Nunley B, Hamid R, Phillips JA, et al. (February 2014). "SHC2 gene copy number in multiple system atrophy (MSA)". Clinical Autonomic Research. 24 (1): 25–30. doi:10.1007/s10286-013-0216-8. PMC 3946192. PMID 24170347.{{cite journal}}: CS1 maint: overridden setting (link)
Sullivan R, Yau WY, Chelban V, Rossi S, O'Connor E, Wood NW, et al. (July 2020). "RFC1 Intronic Repeat Expansions Absent in Pathologically Confirmed Multiple Systems Atrophy". Movement Disorders. 35 (7): 1277–1279. doi:10.1002/mds.28074. PMID 32333430. S2CID 216129457.{{cite journal}}: CS1 maint: overridden setting (link)
Cortese A, Simone R, Sullivan R, Vandrovcova J, Tariq H, Yau WY, et al. (April 2019). "Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia". Nature Genetics. 51 (4): 649–658. doi:10.1038/s41588-019-0372-4. PMC 6709527. PMID 30926972.{{cite journal}}: CS1 maint: overridden setting (link)
Wenning GK, Colosimo C, Geser F, Poewe W (February 2004). "Multiple system atrophy". The Lancet. Neurology. 3 (2): 93–103. doi:10.1016/S1474-4422(03)00662-8. PMID 14747001. S2CID 10162139.
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Jellinger KA, Lantos PL (June 2010). "Papp-Lantos inclusions and the pathogenesis of multiple system atrophy: an update". Acta Neuropathologica. 119 (6): 657–667. doi:10.1007/s00401-010-0672-3. PMID 20309568. S2CID 19759468.
Arima K, Uéda K, Sunohara N, Arakawa K, Hirai S, Nakamura M, et al. (November 1998). "NACP/alpha-synuclein immunoreactivity in fibrillary components of neuronal and oligodendroglial cytoplasmic inclusions in the pontine nuclei in multiple system atrophy". Acta Neuropathologica. 96 (5): 439–444. doi:10.1007/s004010050917. PMID 9829806. S2CID 10804119.{{cite journal}}: CS1 maint: overridden setting (link)
Al-Chalabi A, Dürr A, Wood NW, Parkinson MH, Camuzat A, Hulot JS, et al. (September 2009). "Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy". PLOS ONE. 4 (9): e7114. Bibcode:2009PLoSO...4.7114A. doi:10.1371/journal.pone.0007114. PMC 2743996. PMID 19771175.{{cite journal}}: CS1 maint: overridden setting (link)
Stefanova N, Wenning GK (February 2016). "Review: Multiple system atrophy: emerging targets for interventional therapies". Neuropathology and Applied Neurobiology. 42 (1): 20–32. doi:10.1111/nan.12304. PMC 4788141. PMID 26785838.
De Nuccio F, Kashyrina M, Serinelli F, Laferrière F, Lofrumento DD, De Giorgi F, et al. (February 2023). "Oligodendrocytes Prune Axons Containing α-Synuclein Aggregates In Vivo: Lewy Neurites as Precursors of Glial Cytoplasmic Inclusions in Multiple System Atrophy?". Biomolecules. 13 (2): 269. doi:10.3390/biom13020269. PMC 9953613. PMID 36830639.
Piao YS, Hayashi S, Hasegawa M, Wakabayashi K, Yamada M, Yoshimoto M, et al. (March 2001). "Co-localization of alpha-synuclein and phosphorylated tau in neuronal and glial cytoplasmic inclusions in a patient with multiple system atrophy of long duration". Acta Neuropathologica. 101 (3): 285–293. doi:10.1007/s004010000292. PMID 11307630. S2CID 25650403.{{cite journal}}: CS1 maint: overridden setting (link)
Gilman S, Low PA, Quinn N, Albanese A, Ben-Shlomo Y, Fowler CJ, et al. (February 1999). "Consensus statement on the diagnosis of multiple system atrophy". Journal of the Neurological Sciences. 163 (1): 94–98. doi:10.1016/s0022-510x(98)00304-9. hdl:2027.42/41757. PMID 10223419. S2CID 13307970.{{cite journal}}: CS1 maint: overridden setting (link)
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Wenning GK, Stankovic I, Vignatelli L, Fanciulli A, Calandra-Buonaura G, Seppi K, et al. (2022). "The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy". Movement Disorders. 37 (6): 1131–48. doi:10.1002/mds.29005. hdl:11585/899814. PMC 9321158. PMID 35445419.
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Berciano J, Boesch S, Pérez-Ramos JM, Wenning GK (2006). "Olivopontocerebellar atrophy: toward a better nosological definition". Mov. Disord. 21 (10): 1607–13. doi:10.1002/mds.21052. PMID 16874757. S2CID 38376147.
Papp MI, Kahn JE, Lantos PL (December 1989). "Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)". Journal of the Neurological Sciences. 94 (1–3): 79–100. doi:10.1016/0022-510X(89)90219-0. PMID 2559165. S2CID 1199951.
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Hass EW, Sorrentino ZA, Xia Y, Lloyd GM, Trojanowski JQ, Prokop S, et al. (August 2021). "Disease-, region- and cell type specific diversity of α-synuclein carboxy terminal truncations in synucleinopathies". Acta Neuropathologica Communications. 9 (1): 146. doi:10.1186/s40478-021-01242-2. PMC 8403399. PMID 34454615.
Dhillon JS, Trejo-Lopez JA, Riffe C, McFarland NR, Hiser WM, Giasson BI, et al. (July 2019). "Dissecting α-synuclein inclusion pathology diversity in multiple system atrophy: implications for the prion-like transmission hypothesis". Laboratory Investigation; A Journal of Technical Methods and Pathology. 99 (7): 982–992. doi:10.1038/s41374-019-0198-9. PMC 7209695. PMID 30737468.
Shahnawaz M, Mukherjee A, Pritzkow S, Mendez N, Rabadia P, Liu X, et al. (February 2020). "Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy". Nature. 578 (7794): 273–277. Bibcode:2020Natur.578..273S. doi:10.1038/s41586-020-1984-7. PMC 7066875. PMID 32025029.{{cite journal}}: CS1 maint: overridden setting (link)
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ncbi.nlm.nih.gov

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Sasaki H, Emi M, Iijima H, Ito N, Sato H, Yabe I, et al. (June 2011). "Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy". Molecular Brain. 4: 24. doi:10.1186/1756-6606-4-24. PMC 3141657. PMID 21658278. Copy number loss of SHC2 strongly indicates a causal link to MSA.{{cite journal}}: CS1 maint: overridden setting (link)
Ferguson MC, Garland EM, Hedges L, Womack-Nunley B, Hamid R, Phillips JA, et al. (February 2014). "SHC2 gene copy number in multiple system atrophy (MSA)". Clinical Autonomic Research. 24 (1): 25–30. doi:10.1007/s10286-013-0216-8. PMC 3946192. PMID 24170347.{{cite journal}}: CS1 maint: overridden setting (link)
Cortese A, Simone R, Sullivan R, Vandrovcova J, Tariq H, Yau WY, et al. (April 2019). "Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia". Nature Genetics. 51 (4): 649–658. doi:10.1038/s41588-019-0372-4. PMC 6709527. PMID 30926972.{{cite journal}}: CS1 maint: overridden setting (link)
Al-Chalabi A, Dürr A, Wood NW, Parkinson MH, Camuzat A, Hulot JS, et al. (September 2009). "Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy". PLOS ONE. 4 (9): e7114. Bibcode:2009PLoSO...4.7114A. doi:10.1371/journal.pone.0007114. PMC 2743996. PMID 19771175.{{cite journal}}: CS1 maint: overridden setting (link)
Stefanova N, Wenning GK (February 2016). "Review: Multiple system atrophy: emerging targets for interventional therapies". Neuropathology and Applied Neurobiology. 42 (1): 20–32. doi:10.1111/nan.12304. PMC 4788141. PMID 26785838.
De Nuccio F, Kashyrina M, Serinelli F, Laferrière F, Lofrumento DD, De Giorgi F, et al. (February 2023). "Oligodendrocytes Prune Axons Containing α-Synuclein Aggregates In Vivo: Lewy Neurites as Precursors of Glial Cytoplasmic Inclusions in Multiple System Atrophy?". Biomolecules. 13 (2): 269. doi:10.3390/biom13020269. PMC 9953613. PMID 36830639.
Gilman S, Wenning GK, Low PA, Brooks DJ, Mathias CJ, Trojanowski JQ, et al. (August 2008). "Second consensus statement on the diagnosis of multiple system atrophy". Neurology. 71 (9): 670–676. doi:10.1212/01.wnl.0000324625.00404.15. PMC 2676993. PMID 18725592.{{cite journal}}: CS1 maint: overridden setting (link)
Wenning GK, Stankovic I, Vignatelli L, Fanciulli A, Calandra-Buonaura G, Seppi K, et al. (2022). "The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy". Movement Disorders. 37 (6): 1131–48. doi:10.1002/mds.29005. hdl:11585/899814. PMC 9321158. PMID 35445419.
Koga S, Aoki N, Uitti RJ, van Gerpen JA, Cheshire WP, Josephs KA, et al. (August 2015). "When DLB, PD, and PSP masquerade as MSA: an autopsy study of 134 patients". Neurology. 85 (5): 404–412. doi:10.1212/WNL.0000000000001807. PMC 4534078. PMID 26138942.{{cite journal}}: CS1 maint: overridden setting (link)
"Olivopontocerebellar atrophy - PubMed Health". Archived from the original on 17 November 2012. Retrieved 7 September 2017.
Waxman EA, Giasson BI (July 2009). "Molecular mechanisms of alpha-synuclein neurodegeneration". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1792 (7): 616–624. doi:10.1016/j.bbadis.2008.09.013. PMC 2756732. PMID 18955133.
Burn DJ, Jaros E (December 2001). "Multiple system atrophy: cellular and molecular pathology". Molecular Pathology. 54 (6): 419–426. PMC 1187133. PMID 11724918.
Brettschneider J, Suh E, Robinson JL, Fang L, Lee EB, Irwin DJ, et al. (November 2018). "Converging Patterns of α-Synuclein Pathology in Multiple System Atrophy". Journal of Neuropathology and Experimental Neurology. 77 (11): 1005–1016. doi:10.1093/jnen/nly080. PMC 6181179. PMID 30203094.{{cite journal}}: CS1 maint: overridden setting (link)
Hass EW, Sorrentino ZA, Lloyd GM, McFarland NR, Prokop S, Giasson BI (May 2021). "Robust α-synuclein pathology in select brainstem neuronal populations is a potential instigator of multiple system atrophy". Acta Neuropathologica Communications. 9 (1): 80. doi:10.1186/s40478-021-01173-y. PMC 8091528. PMID 33941284.
Hass EW, Sorrentino ZA, Xia Y, Lloyd GM, Trojanowski JQ, Prokop S, et al. (August 2021). "Disease-, region- and cell type specific diversity of α-synuclein carboxy terminal truncations in synucleinopathies". Acta Neuropathologica Communications. 9 (1): 146. doi:10.1186/s40478-021-01242-2. PMC 8403399. PMID 34454615.
Dhillon JS, Trejo-Lopez JA, Riffe C, McFarland NR, Hiser WM, Giasson BI, et al. (July 2019). "Dissecting α-synuclein inclusion pathology diversity in multiple system atrophy: implications for the prion-like transmission hypothesis". Laboratory Investigation; A Journal of Technical Methods and Pathology. 99 (7): 982–992. doi:10.1038/s41374-019-0198-9. PMC 7209695. PMID 30737468.
Shahnawaz M, Mukherjee A, Pritzkow S, Mendez N, Rabadia P, Liu X, et al. (February 2020). "Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy". Nature. 578 (7794): 273–277. Bibcode:2020Natur.578..273S. doi:10.1038/s41586-020-1984-7. PMC 7066875. PMID 32025029.{{cite journal}}: CS1 maint: overridden setting (link)
Goedert M, Jakes R, Spillantini MG (2017). "The Synucleinopathies: Twenty Years On". Journal of Parkinson's Disease (Review). 7 (s1): S51 – S69. doi:10.3233/JPD-179005. PMC 5345650. PMID 28282814.
MeSH Result
Palma JA, Kaufmann H (February 2020). "Management of Orthostatic Hypotension". Continuum. 26 (1): 154–177. doi:10.1212/CON.0000000000000816. PMC 7339914. PMID 31996627.
Palma JA, Redel-Traub G, Porciuncula A, Samaniego-Toro D, Millar Vernetti P, Lui YW, et al. (June 2020). "The impact of supine hypertension on target organ damage and survival in patients with synucleinopathies and neurogenic orthostatic hypotension". Parkinsonism & Related Disorders. 75 (75): 97–104. doi:10.1016/j.parkreldis.2020.04.011. PMC 7415666. PMID 32516630.
Papapetropoulos S, Tuchman A, Laufer D, Papatsoris AG, Papapetropoulos N, Mash DC (March 2007). "Causes of death in multiple system atrophy". Journal of Neurology, Neurosurgery, and Psychiatry. 78 (3): 327–329. doi:10.1136/jnnp.2006.103929. PMC 2117630. PMID 17308296.

ninds.nih.gov

"What is multiple system atrophy?". NIH. Retrieved 25 November 2018.
"NINDS Olivopontocerebellar Atrophy Information Page". Archived from the original on 27 January 2012. Retrieved 7 February 2012.

rarediseases.info.nih.gov

"Olivopontocerebellar atrophy | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program".

practicalneurology.com

"Multiple System Atrophy-D Maybe Something Altogether–Different". Practical Neurology. Retrieved 11 January 2025.

semanticscholar.org

api.semanticscholar.org

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Gilman S, Koeppe RA, Chervin RD, Consens FB, Little R, An H, et al. (July 2003). "REM sleep behavior disorder is related to striatal monoaminergic deficit in MSA". Neurology. 61 (1): 29–34. doi:10.1212/01.wnl.0000073745.68744.94. PMID 12847152. S2CID 9538306.{{cite journal}}: CS1 maint: overridden setting (link)
Sullivan R, Yau WY, Chelban V, Rossi S, O'Connor E, Wood NW, et al. (July 2020). "RFC1 Intronic Repeat Expansions Absent in Pathologically Confirmed Multiple Systems Atrophy". Movement Disorders. 35 (7): 1277–1279. doi:10.1002/mds.28074. PMID 32333430. S2CID 216129457.{{cite journal}}: CS1 maint: overridden setting (link)
Wenning GK, Colosimo C, Geser F, Poewe W (February 2004). "Multiple system atrophy". The Lancet. Neurology. 3 (2): 93–103. doi:10.1016/S1474-4422(03)00662-8. PMID 14747001. S2CID 10162139.
Wenning GK, Colosimo C, Geser F, Poewe W (March 2004). "Erratum". Lancet Neurol. 3 (3): 137. doi:10.1016/S1474-4422(04)00695-7. S2CID 208782339.
Jellinger KA, Lantos PL (June 2010). "Papp-Lantos inclusions and the pathogenesis of multiple system atrophy: an update". Acta Neuropathologica. 119 (6): 657–667. doi:10.1007/s00401-010-0672-3. PMID 20309568. S2CID 19759468.
Arima K, Uéda K, Sunohara N, Arakawa K, Hirai S, Nakamura M, et al. (November 1998). "NACP/alpha-synuclein immunoreactivity in fibrillary components of neuronal and oligodendroglial cytoplasmic inclusions in the pontine nuclei in multiple system atrophy". Acta Neuropathologica. 96 (5): 439–444. doi:10.1007/s004010050917. PMID 9829806. S2CID 10804119.{{cite journal}}: CS1 maint: overridden setting (link)
Piao YS, Hayashi S, Hasegawa M, Wakabayashi K, Yamada M, Yoshimoto M, et al. (March 2001). "Co-localization of alpha-synuclein and phosphorylated tau in neuronal and glial cytoplasmic inclusions in a patient with multiple system atrophy of long duration". Acta Neuropathologica. 101 (3): 285–293. doi:10.1007/s004010000292. PMID 11307630. S2CID 25650403.{{cite journal}}: CS1 maint: overridden setting (link)
Gilman S, Low PA, Quinn N, Albanese A, Ben-Shlomo Y, Fowler CJ, et al. (February 1999). "Consensus statement on the diagnosis of multiple system atrophy". Journal of the Neurological Sciences. 163 (1): 94–98. doi:10.1016/s0022-510x(98)00304-9. hdl:2027.42/41757. PMID 10223419. S2CID 13307970.{{cite journal}}: CS1 maint: overridden setting (link)
Landers M, Adams M, Acosta K, Fox A. (2009). "Challenge-oriented gait and balance training in sporadic olivopontocerebellar atrophy: a case study". J Neurol Phys Ther. 33 (3): 160–168. doi:10.1097/npt.0b013e3181b511f4. PMID 19809395. S2CID 24642594.
Berciano J, Boesch S, Pérez-Ramos JM, Wenning GK (2006). "Olivopontocerebellar atrophy: toward a better nosological definition". Mov. Disord. 21 (10): 1607–13. doi:10.1002/mds.21052. PMID 16874757. S2CID 38376147.
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