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Comparative Effectiveness Research: A Roadmap for Physical Activity and Lifestyle Jakicic, John M.; Sox, Harold; Blair, Steven N.; Bensink, Mark; Johnson, William G.; King, Abby C.; Lee, I-min; Nahum-Shani, Inbal; Sallis, James F.; Sallis, Robert E.; Craft, Lynette; Whitehead, James R.; Ainsworth, Barbara E. 分享 收藏
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Automated Assessment of Bradykinesia and Dyskinesia in Parkinson's Disease Griffiths, Robert I.; Kotschet, Katya; Arfon, Sian; Xu, Zheng Ming; Johnson, William; Drago, John; Evans, Andrew; Kempster, Peter; Raghav, Sanjay; Horne, Malcolm K. 分享 收藏
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Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis Wisniewski, KE; Zhong, N; Kaczmarski, W; Kaczmarski, A; Kida, E; Brown, WT; Schwarz, KO; Lazzarini, AM; Rubin, AJ; Stenroos, ES; Johnson, WG; Wisniewski, TM 分享 收藏
The α-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease:: A study of 230 European cases Vaughan, J; Durr, A; Tassin, J; Bereznai, B; Gasser, T; Bonifati, V; De Michele, G; Fabrizio, E; Volpe, G; Bandmann, O; Johnson, WG; Golbe, LI; Breteler, M; Meco, G; Agid, Y; Brice, A; Marsden, CD; Wood, NW 分享 收藏
Low frequency of α-synuclein mutations in familial Parkinson's disease Farrer, M; Wavrant-De Vrieze, F; Crook, R; Boles, L; Perez-Tur, J; Hardy, J; Johnson, WG; Steele, J; Maraganore, D; Gwinn, K; Lynch, T 分享 收藏
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Studies of penetrance and anticipation in five autosomal-dominant restless legs syndrome pedigrees Lazzarini, A; Walters, AS; Hickey, K; Coccagna, G; Lugaresi, E; Ehrenberg, BL; Picchietti, DL; Brin, MF; Stenroos, ES; Verrico, T; Johnson, WG 分享 收藏
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