Year |
Citation |
Score |
2020 |
Shivji S, Wong W, Fischer CE, Fornazzari LR, Masellis M, Keith J. Parkinsonism in C9orf72 expansion without co-existing Lewy body pathology; a case report and review of the literature. Neuropathology and Applied Neurobiology. PMID 32339329 DOI: 10.1111/Nan.12623 |
0.307 |
|
2019 |
Shellikeri S, Keith J, Black SE, Zinman L, Yunusova Y. Neuropathology of Speech Network Distinguishes Bulbar From Nonbulbar Amyotrophic Lateral Sclerosis. Journal of Neuropathology and Experimental Neurology. PMID 31951003 DOI: 10.1093/Jnen/Nlz130 |
0.317 |
|
2017 |
Hirsch-Reinshagen V, Pottier C, Nicholson AM, Baker M, Hsiung GR, Krieger C, Sengdy P, Boylan KB, Dickson DW, Mesulam M, Weintraub S, Bigio E, Zinman L, Keith J, Rogaeva E, et al. Clinical and neuropathological features of ALS/FTD with TIA1 mutations. Acta Neuropathologica Communications. 5: 96. PMID 29216908 DOI: 10.1017/Cjn.2018.48 |
0.345 |
|
2017 |
Mackenzie IR, Nicholson AM, Sarkar M, Messing J, Purice MD, Pottier C, Annu K, Baker M, Perkerson RB, Kurti A, Matchett BJ, Mittag T, Temirov J, Hsiung GR, Krieger C, ... ... Keith J, et al. TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics. Neuron. 95: 808-816.e9. PMID 28817800 DOI: 10.1016/J.Neuron.2017.07.025 |
0.309 |
|
2017 |
Keith J, Gao FQ, Noor R, Kiss A, Balasubramaniam G, Au K, Rogaeva E, Masellis M, Black SE. Collagenosis of the Deep Medullary Veins: An Underrecognized Pathologic Correlate of White Matter Hyperintensities and Periventricular Infarction? Journal of Neuropathology and Experimental Neurology. 76: 299-312. PMID 28431180 DOI: 10.1093/Jnen/Nlx009 |
0.305 |
|
2015 |
Xi Z, van Blitterswijk M, Zhang M, McGoldrick P, McLean JR, Yunusova Y, Knock E, Moreno D, Sato C, McKeever PM, Schneider R, Keith J, Petrescu N, Fraser P, Tartaglia MC, et al. Jump from Pre-mutation to Pathologic Expansion in C9orf72. American Journal of Human Genetics. 96: 962-70. PMID 26004200 DOI: 10.1016/J.Ajhg.2015.04.016 |
0.302 |
|
2008 |
Korngut L, Siu VM, Venance SL, Levin S, Ray P, Lemmers RJLF, Keith J, Campbell C. Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophy. Neuromuscular Disorders. 18: 579-582. PMID 18586493 DOI: 10.1016/J.Nmd.2008.03.011 |
0.3 |
|
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