Singleton, Andrew
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Singleton, Andrew
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Results 1-3 of 3 (Search time: 0.003 seconds).
| Issue Date | Title | Author(s) | Type | Access | |
|---|---|---|---|---|---|
| 1 | 2008 | Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3 | Okubadejo, Njideka; Britton, Angela; Crews, Cynthia; Akinyemi, Rufus; Hardy, John ; Singleton, Andrew ; Brás, José | article | openAccess |
| 2 | 2013 | NOTCH3 variants and risk of ischemic stroke | Ross, Owen A.; Soto-Ortolaza, Alexandra I.; Heckman, Michael G.; Verbeeck, Christophe; Serie, Daniel J.; Rayaprolu, Sruti; Rich, Stephen S.; Nalls, Michael A. ; Singleton, Andrew ; Guerreiro, Rita ; Kinsella, Emma; Wszolek, Zbigniew K.; Brott, Thomas G.; Brown, Robert D.; Worrall, Bradford B.; Meschia, James F. | article | openAccess |
| 3 | 11-Jun-2008 | TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis | Guerreiro, Rita ; Schymick, Jennifer C.; Crews, Cynthia; Singleton, Andrew ; Hardy, John ; Traynor, Bryan J. | article | openAccess |