未登录 分享 收藏
分享 收藏
分享 收藏
分享 收藏
分享 收藏
分享 收藏
Temporal Discrimination, a Cervical Dystonia Endophenotype: Penetrance and Functional Correlates 时间歧视，宫颈肌张力障碍内表型: 外显率和功能相关性 Kimmich, Okka; Molloy, Anna; Whelan, Robert; Williams, Laura; Bradley, David; Balsters, Joshua; Molloy, Fiona; Lynch, Tim; Healy, Daniel G.; Walsh, Cathal; O'Riordan, Sean; Reilly, Richard B.; Hutchinson, Michael 分享 收藏
PARKIN DISEASE-A CLINICOPATHOLOGICAL ENTITY? Doherty, Karen M.; Silveira-Moriyama, Laura; Parkkinen, Laura; Healy, Daniel G.; Farrell, Michael; Mencacci, Niccolo E.; Ahmed, Zeshan; Brett, Francesca M.; Hardy, John; Quinn, Niall; Counihan, Timothy J.; Lynch, Timothy; Fox, Zoe V.; Revesz, Tamas; Lees, Andrew J.; Holton, Janice L. 分享 收藏
The Endophenotype and the Phenotype: Temporal Discrimination and Adult-Onset Dystonia Hutchinson, Michael; Kimmich, Okka; Molloy, Anna; Whelan, Robert; Molloy, Fiona; Lynch, Tim; Healy, Daniel G.; Walsh, Cathal; Edwards, Mark J.; Ozelius, Laurie; Reilly, Richard B.; O'Riordan, Sean 分享 收藏
分享 收藏
G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization Papkovskaia, Tatiana D.; Chau, Kai-Yin; Inesta-Vaquera, Francisco; Papkovsky, Dmitri B.; Healy, Daniel G.; Nishio, Koji; Staddon, James; Duchen, Michael R.; Hardy, John; Schapira, Anthony H. V.; Cooper, J. Mark 分享 收藏
分享 收藏
Evidence for Pre and Postsynaptic Nigrostriatal Dysfunction in the Fragile X Tremor-Ataxia Syndrome Healy, Daniel G.; Bressman, Susan; Dickson, John; Silveira-Moriyama, Laura; Schneider, Susanne A.; Sullivan, Sean S. O.; Massey, Luke; Bhatia, Kailash P.; Shaw, Karen; Bomanji, Jamshed; Wood, Nicholas W.; Lees, Andrew J. 分享 收藏
A heterozygous effect for PINK1 mutations in Parkinson's disease? Abou-Sleiman, Patrick M.; Muqit, Miratul M. K.; McDonald, Neil Q.; Yang, Yan Xiang; Gandhi, Sonia; Healy, Daniel G.; Harvey, Kirsten; Harvey, Robert J.; Deas, Emma; Hatia, Kailash; Quinn, Niall; Lees, Andrew; Latchman, David S.; Wood, Nicholas W. 分享 收藏
NR4A2 genetic variation in sporadic Parkinson's disease: A genewide approach 散发性帕金森病的NR4A2遗传变异: 全基因方法 Healy, Daniel G.; Abou-Sleiman, Patrick M.; Ahmadi, Kourosh R.; Gandhi, Sonia; Muqit, Miratul M.; Bhatia, Kailash P.; Quinn, Niall P.; Lees, Andrew J.; Holton, Janice L.; Revesz, Tamas; Wood, Nicholas W. 分享 收藏
分享 收藏
UCHL-1 is not a Parkinson's disease susceptibility gene Healy, DG; Abou-Sleiman, PM; Casas, JP; Ahmadi, KR; Lynch, T; Gandhi, S; Muqit, MMK; Foltynie, T; Barker, R; Bhatia, KP; Quinn, NP; Lees, AJ; Gibson, JM; Holton, JL; Revesz, T; Goldstein, DB; Wood, NW 分享 收藏
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease:: clinical, pathological, olfactory and functional imaging and genetic data Khan, NL; Jain, S; Lynch, JM; Pavese, N; Abou-Sleiman, P; Holton, JL; Healy, DG; Gilks, WP; Sweeney, MG; Ganguly, M; Gibbons, V; Gandhi, S; Vaughan, J; Eunson, LH; Katzenschlager, R; Gayton, J; Lennox, G; Revesz, T; Nicholl, D; Bhatia, KP; Quinn, N; Brooks, D; Lees, AJ; Davis, MB; Piccini, P; Singleton, AB; Wood, NW 分享 收藏
分享 收藏
UCHL-1 gene in multiple system atrophy:: A haplotype tagging approach Healy, DG; Abou-Sleiman, PM; Quinn, N; Ahmadi, KR; Ozawa, T; Kamm, C; Wullner, U; Oertel, WH; Burk, K; Dupont, E; Pellecchia, MT; Tolosa, E; Gasser, T; Holton, JL; Revesz, T; Goldstein, DB; Lees, AJ; Wood, NW 分享 收藏
.png){kind=icon}
未登录.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
