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Items: 1 to 20 of 118

1.

Definite familial multiple system atrophy with unknown genetics.

Itoh K, Kasai T, Tsuji Y, Saito K, Mizuta I, Harada Y, Sudoh S, Mizuno T, Nakagawa M, Fushiki S.

Neuropathology. 2014 Jun;34(3):309-13. doi: 10.1111/neup.12092. Epub 2014 Jan 7.

PMID:
24397755
2.

Genetic players in multiple system atrophy: unfolding the nature of the beast.

Stemberger S, Scholz SW, Singleton AB, Wenning GK.

Neurobiol Aging. 2011 Oct;32(10):1924.e5-14. doi: 10.1016/j.neurobiolaging.2011.04.001. Epub 2011 May 24.

3.

Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.

Al-Chalabi A, Dürr A, Wood NW, Parkinson MH, Camuzat A, Hulot JS, Morrison KE, Renton A, Sussmuth SD, Landwehrmeyer BG, Ludolph A, Agid Y, Brice A, Leigh PN, Bensimon G; NNIPPS Genetic Study Group.

PLoS One. 2009 Sep 22;4(9):e7114. doi: 10.1371/journal.pone.0007114.

4.

Analysis of COQ2 gene in multiple system atrophy.

Ogaki K, Fujioka S, Heckman MG, Rayaprolu S, Soto-Ortolaza AI, Labbé C, Walton RL, Lorenzo-Betancor O, Wang X, Asmann Y, Rademakers R, Graff-Radford N, Uitti R, Cheshire WP, Wszolek ZK, Dickson DW, Ross OA.

Mol Neurodegener. 2014 Nov 5;9:44. doi: 10.1186/1750-1326-9-44.

5.

The neuropathology, pathophysiology and genetics of multiple system atrophy.

Ahmed Z, Asi YT, Sailer A, Lees AJ, Houlden H, Revesz T, Holton JL.

Neuropathol Appl Neurobiol. 2012 Feb;38(1):4-24. doi: 10.1111/j.1365-2990.2011.01234.x. Review.

PMID:
22074330
6.

"Preclinical" MSA in definite Creutzfeldt-Jakob disease.

Rodriguez-Diehl R, Rey MJ, Gironell A, Martinez-Saez E, Ferrer I, Sánchez-Valle R, Jagüe J, Nos C, Gelpi E.

Neuropathology. 2012 Apr;32(2):158-63. doi: 10.1111/j.1440-1789.2011.01232.x. Epub 2011 Jun 21.

PMID:
21692862
7.

Quantitative PCR-based screening of alpha-synuclein multiplication in multiple system atrophy.

Lincoln SJ, Ross OA, Milkovic NM, Dickson DW, Rajput A, Robinson CA, Papapetropoulos S, Mash DC, Farrer MJ.

Parkinsonism Relat Disord. 2007 Aug;13(6):340-2. Epub 2007 Feb 8.

8.

Multiplex families with multiple system atrophy.

Hara K, Momose Y, Tokiguchi S, Shimohata M, Terajima K, Onodera O, Kakita A, Yamada M, Takahashi H, Hirasawa M, Mizuno Y, Ogata K, Goto J, Kanazawa I, Nishizawa M, Tsuji S.

Arch Neurol. 2007 Apr;64(4):545-51.

PMID:
17420317
9.

Multiple system atrophy: the application of genetics in understanding etiology.

Federoff M, Schottlaender LV, Houlden H, Singleton A.

Clin Auton Res. 2015 Feb;25(1):19-36. doi: 10.1007/s10286-014-0267-5. Epub 2015 Feb 17. Review.

PMID:
25687905
10.

Analyses of copy number and mRNA expression level of the alpha-synuclein gene in multiple system atrophy.

Jin H, Ishikawa K, Tsunemi T, Ishiguro T, Amino T, Mizusawa H.

J Med Dent Sci. 2008 Mar;55(1):145-53.

PMID:
19845160
11.

Papp-Lantos inclusions and the pathogenesis of multiple system atrophy: an update.

Jellinger KA, Lantos PL.

Acta Neuropathol. 2010 Jun;119(6):657-67. doi: 10.1007/s00401-010-0672-3. Epub 2010 Mar 23. Review.

PMID:
20309568
12.

An autopsy case of preclinical multiple system atrophy (MSA-C).

Kon T, Mori F, Tanji K, Miki Y, Wakabayashi K.

Neuropathology. 2013 Dec;33(6):667-72. doi: 10.1111/neup.12037. Epub 2013 Apr 14.

PMID:
23581648
13.

Multiple system atrophy: pathophysiology and management.

Wenning GK, Braune S.

CNS Drugs. 2001;15(11):839-52. Review.

PMID:
11700149
14.

Update on novel familial forms of Parkinson's disease and multiple system atrophy.

Fujioka S, Ogaki K, Tacik PM, Uitti RJ, Ross OA, Wszolek ZK.

Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S29-34. doi: 10.1016/S1353-8020(13)70010-5. Review.

15.

Grading of neuropathology in multiple system atrophy: proposal for a novel scale.

Jellinger KA, Seppi K, Wenning GK.

Mov Disord. 2005 Aug;20 Suppl 12:S29-36.

PMID:
16092088
16.

Multiple system atrophy: an update.

Wenning GK, Geser F, Stampfer-Kountchev M, Tison F.

Mov Disord. 2003 Sep;18 Suppl 6:S34-42.

PMID:
14502654
17.

Role of transcriptional control in multiple system atrophy.

Chen J, Mills JD, Halliday GM, Janitz M.

Neurobiol Aging. 2015 Jan;36(1):394-400. doi: 10.1016/j.neurobiolaging.2014.08.015. Epub 2014 Aug 19. Review.

PMID:
25218777
18.

Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy.

Chen YP, Zhao B, Cao B, Song W, Guo X, Wei QQ, Yang Y, Yuan LX, Shang HF.

Neurobiol Aging. 2015 Feb;36(2):1222.e7-11. doi: 10.1016/j.neurobiolaging.2014.09.010. Epub 2014 Sep 18.

PMID:
25442117
19.

Tau-positive glial cytoplasmic granules in multiple system atrophy.

Nagaishi M, Yokoo H, Nakazato Y.

Neuropathology. 2011 Jun;31(3):299-305. doi: 10.1111/j.1440-1789.2010.01159.x. Epub 2010 Nov 9.

PMID:
21062361
20.

Novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology.

Pasanen P, Myllykangas L, Siitonen M, Raunio A, Kaakkola S, Lyytinen J, Tienari PJ, Pöyhönen M, Paetau A.

Neurobiol Aging. 2014 Sep;35(9):2180.e1-5. doi: 10.1016/j.neurobiolaging.2014.03.024. Epub 2014 Mar 26.

PMID:
24746362
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