Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Multiple System Atrophy and C9orf72[original query] |
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| C9orf72 repeat expansions are a rare genetic cause of parkinsonism. Brain : a journal of neurology 2013 Feb 136 (Pt 2): 385-91. Lesage Suzanne, Le Ber Isabelle, Condroyer Christel, Broussolle Emmanuel, Gabelle Audrey, Thobois Stéphane, Pasquier Florence, Mondon Karl, Dion Patrick A, Rochefort Daniel, Rouleau Guy A, Dürr Alexandra, Brice Alexis, |
| C9ORF72 repeat expansion is not a significant cause of late onset cerebellar ataxia syndrome. Journal of the neurological sciences 2014 Dec 347 (1-2): 322-4. Hsiao Cheng-Tsung, Tsai Pei-Chien, Liao Yi-Chu, Lee Yi-Chung, Soong Bing-W |
| C9ORF72 repeat expansions in Chinese patients with Parkinson's disease and multiple system atrophy. Journal of neural transmission (Vienna, Austria : 1996) 2016 Jul . Chen Xueping, Chen Yongping, Wei Qianqian, Ou Ruwei, Cao Bei, Zhao Bi, Shang Hui-Fa |
| Coexisting Lewy body disease and clinical parkinsonism in frontotemporal lobar degeneration. Neurology 2019 4 92 (21): e2472-e2482. Forrest Shelley L, Crockford Daniel R, Sizemova Anastasia, McCann Heather, Shepherd Claire E, McGeachie Andrew B, Affleck Andrew J, Carew-Jones Francine, Bartley Lauren, Kwok John B, Kim Woojin Scott, Jary Eve, Tan Rachel H, McGinley Ciara V, Piguet Olivier, Hodges John R, Kril Jillian J, Halliday Glenda |
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- Page last updated:Dec 04, 2023
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