Ατροφία πολλαπλών συστημάτων (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ατροφία πολλαπλών συστημάτων" in Greek language version.

refsWebsite

Global rank Greek rank

56nih.gov

4^th place

35doi.org

2^nd place

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3harvard.edu

18^th place

57^th place

3archive.org

6^th place

5^th place

3worldcat.org

5^th place

8^th place

2medscape.com

719^th place

579^th place

2mayoclinic.org

1,610^th place

485^th place

1umich.edu

459^th place

313^th place

1web.archive.org

1^st place

1vanderbilt.edu

3,332^nd place

9,164^th place

1technologynetworks.com

low place

archive.org

«Multiple system atrophy». Phys Ther 79 (5): 488–94. May 1999. doi:10.1093/ptj/79.5.488. PMID 10331752. https://archive.org/details/sim_physical-therapy_1999-05_79_5/page/488.
«NACP/alpha-synuclein immunoreactivity in fibrillary components of neuronal and oligodendroglial cytoplasmic inclusions in the pontine nuclei in multiple system atrophy». Acta Neuropathol. 96 (5): 439–44. November 1998. doi:10.1007/s004010050917. PMID 9829806. https://archive.org/details/sim_acta-neuropathologica_1998-11_96_5/page/439.
The Consensus Committee of the American Autonomic Society and the American Academy of Neurology (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. https://archive.org/details/sim_neurology_1996-05_46_5/page/n337.

doi.org

dx.doi.org

«Cellular milieu imparts distinct pathological α-synuclein strains in α-synucleinopathies». Nature 557 (7706): 558–563. May 2018. doi:10.1038/s41586-018-0104-4. PMID 29743672. Bibcode: 2018Natur.557..558P.
«Multiple-system atrophy». N. Engl. J. Med. 372 (3): 249–63. January 2015. doi:10.1056/NEJMra1311488. PMID 25587949.
«Multiple system atrophy». Phys Ther 79 (5): 488–94. May 1999. doi:10.1093/ptj/79.5.488. PMID 10331752. https://archive.org/details/sim_physical-therapy_1999-05_79_5/page/488.
«Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein». Acta Neuropathol. 130 (1): 93–105. July 2015. doi:10.1007/s00401-015-1442-z. PMID 25962793.
«Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study». Brain 132 (Pt 1): 156–71. January 2009. doi:10.1093/brain/awn291. PMID 19029129.
«Reduced genital sensitivity in female patients with multiple system atrophy of parkinsonian type». Mov. Disord. 18 (4): 430–2. April 2003. doi:10.1002/mds.10384. PMID 12671951.
«REM sleep behavior disorder is related to striatal monoaminergic deficit in MSA». Neurology 61 (1): 29–34. July 2003. doi:10.1212/01.wnl.0000073745.68744.94. PMID 12847152.
«Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy». Brain 133 (Pt 8): 2382–93. August 2010. doi:10.1093/brain/awq158. PMID 20576697.
«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». Mol Brain 4: 24. 2011. doi:10.1186/1756-6606-4-24. PMID 21658278. «Copy number loss of SHC2 strongly indicates a causal link to MSA.».
«SHC2 gene copy number in multiple system atrophy (MSA)». Clin. Auton. Res. 24 (1): 25–30. February 2014. doi:10.1007/s10286-013-0216-8. PMID 24170347.
Sullivan, Roisin; Yau, Wai Yan; Chelban, Viorica; Rossi, Salvatore; O'Connor, E.; Wood, Nicholas W.; Cortese, Andrea; Houlden, Henry (2020-04-24). «RFC1 Intronic Repeat Expansions Absent in Pathologically Confirmed Multiple Systems Atrophy». Movement Disorders 35 (7): 1277–1279. doi:10.1002/mds.28074. ISSN 1531-8257. PMID 32333430.
Cortese, Andrea; Simone, Roberto; Sullivan, Roisin; Vandrovcova, Jana; Tariq, Huma; Yau, Wai Yan; Humphrey, Jack; Jaunmuktane, Zane και άλλοι. (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. ISSN 1546-1718. PMID 30926972.
«Multiple system atrophy». Lancet Neurol 3 (2): 93–103. February 2004. doi:10.1016/S1474-4422(03)00662-8. PMID 14747001.

«Erratum». Lancet Neurol 3 (3): 137. March 2004. doi:10.1016/S1474-4422(04)00695-7.
«Papp-Lantos inclusions and the pathogenesis of multiple system atrophy: an update.». Acta Neuropathol. 119 (6): 657-67. June 2010. doi:10.1007/s00401-010-0672-3. PMID 20309568.
«NACP/alpha-synuclein immunoreactivity in fibrillary components of neuronal and oligodendroglial cytoplasmic inclusions in the pontine nuclei in multiple system atrophy». Acta Neuropathol. 96 (5): 439–44. November 1998. doi:10.1007/s004010050917. PMID 9829806. https://archive.org/details/sim_acta-neuropathologica_1998-11_96_5/page/439.
«Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy». PLOS ONE 4 (9): e7114. September 2009. doi:10.1371/journal.pone.0007114. PMID 19771175. Bibcode: 2009PLoSO...4.7114A.
«Review: Multiple system atrophy: emerging targets for interventional therapies». Neuropathology and Applied Neurobiology 42 (1): 20–32. February 2016. doi:10.1111/nan.12304. PMID 26785838.
«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 Neuropathol. 101 (3): 285–93. March 2001. doi:10.1007/s004010000292. PMID 11307630.
«Consensus statement on the diagnosis of multiple system atrophy». J. Neurol. Sci. 163 (1): 94–8. February 1999. doi:10.1016/s0022-510x(98)00304-9. PMID 10223419. https://deepblue.lib.umich.edu/bitstream/2027.42/41757/1/10286_2006_Article_BF02309628.pdf.
«Second consensus statement on the diagnosis of multiple system atrophy». Neurology 71 (9): 670–6. August 2008. doi:10.1212/01.wnl.0000324625.00404.15. PMID 18725592.
«When DLB, PD, and PSP masquerade as MSA: an autopsy study of 134 patients». Neurology 85 (5): 404–12. August 2015. doi:10.1212/WNL.0000000000001807. PMID 26138942.
«Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)». J. Neurol. Sci. 94 (1–3): 79–100. December 1989. doi:10.1016/0022-510X(89)90219-0. PMID 2559165.
Waxman, EA; Giasson, BI (July 2009). «Molecular mechanisms of alpha-synuclein neurodegeneration.». Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1792 (7): 616–24. doi:10.1016/j.bbadis.2008.09.013. PMID 18955133.
Ozawa, T; Paviour, D; Quinn, NP; Josephs, KA; Sangha, H; Kilford, L; Healy, DG; Wood, NW και άλλοι. (December 2004). «The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations.». Brain : A Journal of Neurology 127 (Pt 12): 2657–71. doi:10.1093/brain/awh303. PMID 15509623.
Brettschneider, J; Suh, E; Robinson, JL; Fang, L; Lee, EB; Irwin, DJ; Grossman, M; Van Deerlin, VM και άλλοι. (1 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. PMID 30203094.
Dhillon, Jess-Karan S.; Trejo-Lopez, Jorge A.; Riffe, Cara; McFarland, Nikolaus R.; Hiser, Wesley M.; Giasson, Benoit I.; Yachnis, Anthony T. (July 2019). «Dissecting α-synuclein inclusion pathology diversity in multiple system atrophy: implications for the prion-like transmission hypothesis». Laboratory Investigation 99 (7): 982–992. doi:10.1038/s41374-019-0198-9. PMID 30737468.
Shahnawaz, Mohammad; Mukherjee, Abhisek; Pritzkow, Sandra; Mendez, Nicolas; Rabadia, Prakruti; Liu, Xiangan; Hu, Bo; Schmeichel, Ann και άλλοι. (5 February 2020). «Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy». Nature 578 (7794): 273–277. doi:10.1038/s41586-020-1984-7. PMID 32025029. Bibcode: 2020Natur.578..273S.
«The Synucleinopathies: Twenty Years On». J Parkinsons Dis 7 (s1): S53–S71. 2017. doi:10.3233/JPD-179005. PMID 28282814.
The Consensus Committee of the American Autonomic Society and the American Academy of Neurology (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. https://archive.org/details/sim_neurology_1996-05_46_5/page/n337.
name="Ahmed-2012">«The neuropathology, pathophysiology and genetics of multiple system atrophy». Neuropathol. Appl. Neurobiol. 38 (1): 4–24. February 2012. doi:10.1111/j.1365-2990.2011.01234.x. PMID 22074330.
«A neurological syndrome associated with orthostatic hypotension: a clinical-pathologic study». Arch. Neurol. 2 (5): 511–27. 1960. doi:10.1001/archneur.1960.03840110025004. PMID 14446364.
«Farewell to the "Shy-Drager syndrome"». Ann. Intern. Med. 125 (1): 74–5. July 1996. doi:10.7326/0003-4819-125-1-199607010-00012. PMID 8644992.
Calandra-Buonaura, Giovanna; Doria, Andrea; Lopane, Giovanna; Guaraldi, Pietro; Capellari, Sabina; Martinelli, Paolo; Cortelli, Pietro; Contin, Manuela (2015). «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. ISSN 0340-5354. PMID 26566913.
«Multiple system atrophy: pathophysiology, treatment and nursing care». Nurs Stand 22 (22): 50–6; quiz 58. 2008. doi:10.7748/ns2008.02.22.22.50.c6359. PMID 18333558.
Papapetropoulos, Spiridon (March 2007). «Causes of death in multiple system atrophy». J Neurol Neurosurg Psychiatry 78 (78,3): 327–329. doi:10.1136/jnnp.2006.103929. PMID 17308296.

harvard.edu

adsabs.harvard.edu

«Cellular milieu imparts distinct pathological α-synuclein strains in α-synucleinopathies». Nature 557 (7706): 558–563. May 2018. doi:10.1038/s41586-018-0104-4. PMID 29743672. Bibcode: 2018Natur.557..558P.
«Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy». PLOS ONE 4 (9): e7114. September 2009. doi:10.1371/journal.pone.0007114. PMID 19771175. Bibcode: 2009PLoSO...4.7114A.
Shahnawaz, Mohammad; Mukherjee, Abhisek; Pritzkow, Sandra; Mendez, Nicolas; Rabadia, Prakruti; Liu, Xiangan; Hu, Bo; Schmeichel, Ann και άλλοι. (5 February 2020). «Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy». Nature 578 (7794): 273–277. doi:10.1038/s41586-020-1984-7. PMID 32025029. Bibcode: 2020Natur.578..273S.

mayoclinic.org

name=MayoMSA>Multiple system atrophy (MSA) mayoclinic.org, accessed 20 May 2018
Multiple system atrophy (MSA) mayoclinic.org, accessed 20 May 2018

medscape.com

emedicine.medscape.com

«Multiple System Atrophy Clinical Presentation». Ανακτήθηκε στις 7 Ιανουαρίου 2018.
multiple system atrophy overview. 2018-09-24. http://emedicine.medscape.com/article/1154074-overview#a2.

nih.gov

ncbi.nlm.nih.gov

«Cellular milieu imparts distinct pathological α-synuclein strains in α-synucleinopathies». Nature 557 (7706): 558–563. May 2018. doi:10.1038/s41586-018-0104-4. PMID 29743672. Bibcode: 2018Natur.557..558P.
«Multiple-system atrophy». N. Engl. J. Med. 372 (3): 249–63. January 2015. doi:10.1056/NEJMra1311488. PMID 25587949.
«Multiple system atrophy». Phys Ther 79 (5): 488–94. May 1999. doi:10.1093/ptj/79.5.488. PMID 10331752. https://archive.org/details/sim_physical-therapy_1999-05_79_5/page/488.
«Multiple system atrophy: cellular and molecular pathology». Mol. Pathol. 54 (6): 419–26. December 2001. PMID 11724918.
«Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein». Acta Neuropathol. 130 (1): 93–105. July 2015. doi:10.1007/s00401-015-1442-z. PMID 25962793.
«Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study». Brain 132 (Pt 1): 156–71. January 2009. doi:10.1093/brain/awn291. PMID 19029129.
«Reduced genital sensitivity in female patients with multiple system atrophy of parkinsonian type». Mov. Disord. 18 (4): 430–2. April 2003. doi:10.1002/mds.10384. PMID 12671951.
«REM sleep behavior disorder is related to striatal monoaminergic deficit in MSA». Neurology 61 (1): 29–34. July 2003. doi:10.1212/01.wnl.0000073745.68744.94. PMID 12847152.
«Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy». Brain 133 (Pt 8): 2382–93. August 2010. doi:10.1093/brain/awq158. PMID 20576697.
«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». Mol Brain 4: 24. 2011. doi:10.1186/1756-6606-4-24. PMID 21658278. «Copy number loss of SHC2 strongly indicates a causal link to MSA.».
«SHC2 gene copy number in multiple system atrophy (MSA)». Clin. Auton. Res. 24 (1): 25–30. February 2014. doi:10.1007/s10286-013-0216-8. PMID 24170347.
Sullivan, Roisin; Yau, Wai Yan; Chelban, Viorica; Rossi, Salvatore; O'Connor, E.; Wood, Nicholas W.; Cortese, Andrea; Houlden, Henry (2020-04-24). «RFC1 Intronic Repeat Expansions Absent in Pathologically Confirmed Multiple Systems Atrophy». Movement Disorders 35 (7): 1277–1279. doi:10.1002/mds.28074. ISSN 1531-8257. PMID 32333430.
Cortese, Andrea; Simone, Roberto; Sullivan, Roisin; Vandrovcova, Jana; Tariq, Huma; Yau, Wai Yan; Humphrey, Jack; Jaunmuktane, Zane και άλλοι. (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. ISSN 1546-1718. PMID 30926972.
«Multiple system atrophy». Lancet Neurol 3 (2): 93–103. February 2004. doi:10.1016/S1474-4422(03)00662-8. PMID 14747001.

«Erratum». Lancet Neurol 3 (3): 137. March 2004. doi:10.1016/S1474-4422(04)00695-7.
«Papp-Lantos inclusions and the pathogenesis of multiple system atrophy: an update.». Acta Neuropathol. 119 (6): 657-67. June 2010. doi:10.1007/s00401-010-0672-3. PMID 20309568.
«NACP/alpha-synuclein immunoreactivity in fibrillary components of neuronal and oligodendroglial cytoplasmic inclusions in the pontine nuclei in multiple system atrophy». Acta Neuropathol. 96 (5): 439–44. November 1998. doi:10.1007/s004010050917. PMID 9829806. https://archive.org/details/sim_acta-neuropathologica_1998-11_96_5/page/439.
«Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy». PLOS ONE 4 (9): e7114. September 2009. doi:10.1371/journal.pone.0007114. PMID 19771175. Bibcode: 2009PLoSO...4.7114A.
«Review: Multiple system atrophy: emerging targets for interventional therapies». Neuropathology and Applied Neurobiology 42 (1): 20–32. February 2016. doi:10.1111/nan.12304. PMID 26785838.
«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 Neuropathol. 101 (3): 285–93. March 2001. doi:10.1007/s004010000292. PMID 11307630.
«Consensus statement on the diagnosis of multiple system atrophy». J. Neurol. Sci. 163 (1): 94–8. February 1999. doi:10.1016/s0022-510x(98)00304-9. PMID 10223419. https://deepblue.lib.umich.edu/bitstream/2027.42/41757/1/10286_2006_Article_BF02309628.pdf.
«Second consensus statement on the diagnosis of multiple system atrophy». Neurology 71 (9): 670–6. August 2008. doi:10.1212/01.wnl.0000324625.00404.15. PMID 18725592.
«When DLB, PD, and PSP masquerade as MSA: an autopsy study of 134 patients». Neurology 85 (5): 404–12. August 2015. doi:10.1212/WNL.0000000000001807. PMID 26138942.
«Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome)». J. Neurol. Sci. 94 (1–3): 79–100. December 1989. doi:10.1016/0022-510X(89)90219-0. PMID 2559165.
Waxman, EA; Giasson, BI (July 2009). «Molecular mechanisms of alpha-synuclein neurodegeneration.». Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1792 (7): 616–24. doi:10.1016/j.bbadis.2008.09.013. PMID 18955133.
Burn, DJ; Jaros, E (December 2001). «Multiple system atrophy: cellular and molecular pathology.». Molecular Pathology : MP 54 (6): 419–26. PMID 11724918.
Ozawa, T; Paviour, D; Quinn, NP; Josephs, KA; Sangha, H; Kilford, L; Healy, DG; Wood, NW και άλλοι. (December 2004). «The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations.». Brain : A Journal of Neurology 127 (Pt 12): 2657–71. doi:10.1093/brain/awh303. PMID 15509623.
Brettschneider, J; Suh, E; Robinson, JL; Fang, L; Lee, EB; Irwin, DJ; Grossman, M; Van Deerlin, VM και άλλοι. (1 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. PMID 30203094.
Dhillon, Jess-Karan S.; Trejo-Lopez, Jorge A.; Riffe, Cara; McFarland, Nikolaus R.; Hiser, Wesley M.; Giasson, Benoit I.; Yachnis, Anthony T. (July 2019). «Dissecting α-synuclein inclusion pathology diversity in multiple system atrophy: implications for the prion-like transmission hypothesis». Laboratory Investigation 99 (7): 982–992. doi:10.1038/s41374-019-0198-9. PMID 30737468.
Shahnawaz, Mohammad; Mukherjee, Abhisek; Pritzkow, Sandra; Mendez, Nicolas; Rabadia, Prakruti; Liu, Xiangan; Hu, Bo; Schmeichel, Ann και άλλοι. (5 February 2020). «Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy». Nature 578 (7794): 273–277. doi:10.1038/s41586-020-1984-7. PMID 32025029. Bibcode: 2020Natur.578..273S.
«The Synucleinopathies: Twenty Years On». J Parkinsons Dis 7 (s1): S53–S71. 2017. doi:10.3233/JPD-179005. PMID 28282814.
The Consensus Committee of the American Autonomic Society and the American Academy of Neurology (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. https://archive.org/details/sim_neurology_1996-05_46_5/page/n337.
name="Ahmed-2012">«The neuropathology, pathophysiology and genetics of multiple system atrophy». Neuropathol. Appl. Neurobiol. 38 (1): 4–24. February 2012. doi:10.1111/j.1365-2990.2011.01234.x. PMID 22074330.
«A neurological syndrome associated with orthostatic hypotension: a clinical-pathologic study». Arch. Neurol. 2 (5): 511–27. 1960. doi:10.1001/archneur.1960.03840110025004. PMID 14446364.
«Farewell to the "Shy-Drager syndrome"». Ann. Intern. Med. 125 (1): 74–5. July 1996. doi:10.7326/0003-4819-125-1-199607010-00012. PMID 8644992.
Calandra-Buonaura, Giovanna; Doria, Andrea; Lopane, Giovanna; Guaraldi, Pietro; Capellari, Sabina; Martinelli, Paolo; Cortelli, Pietro; Contin, Manuela (2015). «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. ISSN 0340-5354. PMID 26566913.
«Multiple system atrophy: pathophysiology, treatment and nursing care». Nurs Stand 22 (22): 50–6; quiz 58. 2008. doi:10.7748/ns2008.02.22.22.50.c6359. PMID 18333558.
Papapetropoulos, Spiridon (March 2007). «Causes of death in multiple system atrophy». J Neurol Neurosurg Psychiatry 78 (78,3): 327–329. doi:10.1136/jnnp.2006.103929. PMID 17308296.

pubmedcentral.nih.gov

«Cellular milieu imparts distinct pathological α-synuclein strains in α-synucleinopathies». Nature 557 (7706): 558–563. May 2018. doi:10.1038/s41586-018-0104-4. PMID 29743672. Bibcode: 2018Natur.557..558P.
«Multiple system atrophy: cellular and molecular pathology». Mol. Pathol. 54 (6): 419–26. December 2001. PMID 11724918.
«Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein». Acta Neuropathol. 130 (1): 93–105. July 2015. doi:10.1007/s00401-015-1442-z. PMID 25962793.
«Riluzole treatment, survival and diagnostic criteria in Parkinson plus disorders: the NNIPPS study». Brain 132 (Pt 1): 156–71. January 2009. doi:10.1093/brain/awn291. PMID 19029129.
«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». Mol Brain 4: 24. 2011. doi:10.1186/1756-6606-4-24. PMID 21658278. «Copy number loss of SHC2 strongly indicates a causal link to MSA.».
«SHC2 gene copy number in multiple system atrophy (MSA)». Clin. Auton. Res. 24 (1): 25–30. February 2014. doi:10.1007/s10286-013-0216-8. PMID 24170347.
Cortese, Andrea; Simone, Roberto; Sullivan, Roisin; Vandrovcova, Jana; Tariq, Huma; Yau, Wai Yan; Humphrey, Jack; Jaunmuktane, Zane και άλλοι. (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. ISSN 1546-1718. PMID 30926972.
«Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy». PLOS ONE 4 (9): e7114. September 2009. doi:10.1371/journal.pone.0007114. PMID 19771175. Bibcode: 2009PLoSO...4.7114A.
«Review: Multiple system atrophy: emerging targets for interventional therapies». Neuropathology and Applied Neurobiology 42 (1): 20–32. February 2016. doi:10.1111/nan.12304. PMID 26785838.
«Second consensus statement on the diagnosis of multiple system atrophy». Neurology 71 (9): 670–6. August 2008. doi:10.1212/01.wnl.0000324625.00404.15. PMID 18725592.
«When DLB, PD, and PSP masquerade as MSA: an autopsy study of 134 patients». Neurology 85 (5): 404–12. August 2015. doi:10.1212/WNL.0000000000001807. PMID 26138942.
Waxman, EA; Giasson, BI (July 2009). «Molecular mechanisms of alpha-synuclein neurodegeneration.». Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1792 (7): 616–24. doi:10.1016/j.bbadis.2008.09.013. PMID 18955133.
Burn, DJ; Jaros, E (December 2001). «Multiple system atrophy: cellular and molecular pathology.». Molecular Pathology : MP 54 (6): 419–26. PMID 11724918.
Brettschneider, J; Suh, E; Robinson, JL; Fang, L; Lee, EB; Irwin, DJ; Grossman, M; Van Deerlin, VM και άλλοι. (1 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. PMID 30203094.
Dhillon, Jess-Karan S.; Trejo-Lopez, Jorge A.; Riffe, Cara; McFarland, Nikolaus R.; Hiser, Wesley M.; Giasson, Benoit I.; Yachnis, Anthony T. (July 2019). «Dissecting α-synuclein inclusion pathology diversity in multiple system atrophy: implications for the prion-like transmission hypothesis». Laboratory Investigation 99 (7): 982–992. doi:10.1038/s41374-019-0198-9. PMID 30737468.
Shahnawaz, Mohammad; Mukherjee, Abhisek; Pritzkow, Sandra; Mendez, Nicolas; Rabadia, Prakruti; Liu, Xiangan; Hu, Bo; Schmeichel, Ann και άλλοι. (5 February 2020). «Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy». Nature 578 (7794): 273–277. doi:10.1038/s41586-020-1984-7. PMID 32025029. Bibcode: 2020Natur.578..273S.
«The Synucleinopathies: Twenty Years On». J Parkinsons Dis 7 (s1): S53–S71. 2017. doi:10.3233/JPD-179005. PMID 28282814.
Papapetropoulos, Spiridon (March 2007). «Causes of death in multiple system atrophy». J Neurol Neurosurg Psychiatry 78 (78,3): 327–329. doi:10.1136/jnnp.2006.103929. PMID 17308296.

ninds.nih.gov

«What is multiple system atrophy?». NIH. Ανακτήθηκε στις 25 Νοεμβρίου 2018.

technologynetworks.com

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umich.edu

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vanderbilt.edu

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web.archive.org

Vanderbilt Autonomic Dysfunction Cente. «Multiple System Atrophy / Shy Drager Syndrome». Αρχειοθετήθηκε από το πρωτότυπο στις 14 Μαΐου 2011. Ανακτήθηκε στις 29 Μαΐου 2010.

worldcat.org

Sullivan, Roisin; Yau, Wai Yan; Chelban, Viorica; Rossi, Salvatore; O'Connor, E.; Wood, Nicholas W.; Cortese, Andrea; Houlden, Henry (2020-04-24). «RFC1 Intronic Repeat Expansions Absent in Pathologically Confirmed Multiple Systems Atrophy». Movement Disorders 35 (7): 1277–1279. doi:10.1002/mds.28074. ISSN 1531-8257. PMID 32333430.
Cortese, Andrea; Simone, Roberto; Sullivan, Roisin; Vandrovcova, Jana; Tariq, Huma; Yau, Wai Yan; Humphrey, Jack; Jaunmuktane, Zane και άλλοι. (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. ISSN 1546-1718. PMID 30926972.
Calandra-Buonaura, Giovanna; Doria, Andrea; Lopane, Giovanna; Guaraldi, Pietro; Capellari, Sabina; Martinelli, Paolo; Cortelli, Pietro; Contin, Manuela (2015). «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. ISSN 0340-5354. PMID 26566913.