Autosomal dominant cerebellar ataxia type III: No evidence for a large pathological CAG repeat expansion in the SCA 11 gene. by Worth, P, Dunne, E, Nemeth, A, Wood, N

Mediated electron transfer from lithium investigated voltammetrically in tetrahydrofuran: why are some mediators more effective reducing reagents than others? by Wood, N, Paddon, C, Bhatti, F, Donohoe, T, Compton, R

Childhood correlates of adult positive mental well-being in three British longitudinal studies by Wood, N, Hardy, R, Bann, D, Gale, C, Stafford, M

A luohan from Yixian in the Heritage Museum: Some Parallels in Material Usage with the Longquanwu and Liuliqu kilns near Beijing by Wood, N, Doherty, C, Menshikova, M, Eng, C, Smithies, R

Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look-alike? by Warren, J, Mummery, C, Al-Din, A, Brown, P, Wood, N

New insights for the calcium flux used in ancient Longquan and Yue kiln based on the Sr isotopic compositions by Ma, H, Wood, N, Doherty, C, Zheng, J, Zhou, G, Duan, H

Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug-responsive splice variants of SCN1A. by Heinzen, E, Yoon, W, Tate, S, Sen, A, Wood, N, Sisodiya, S, Goldstein, D

Motor cortical physiology in patients and asymptomatic carriers of parkin gene mutations. by Schneider, SA, Talelli, P, Cheeran, B, Khan, N, Wood, N, Rothwell, J, Bhatia, K

Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats. by Ansorge, O, Giunti, P, Michalik, A, Van Broeckhoven, C, Harding, B, Wood, N, Scaravilli, F

Peripheral Serotonin 1B receptor transcription predicts the effect of acute Tryptophan depletion on risky decision-making by Faulkner, P, Mancinelli, F, Lockwood, P, Matarin, M, Dolan, R, Wood, N, Dayan, P, Roiser, J

Changsha ware glaze color: Composition, nanostructure, and copper and iron speciation by Yuan, M, Hou, J, Zhang, X, Wood, N, Molera, J, Castillo‐Michel, H, Cotte, M, Pradell, T

Neuronal intranuclear inclusions in SCA2: A genetic, morphological and immunohistochemical study of two cases by Pang, J, Giunti, P, Chamberlain, S, An, S, Vitaliani, R, Scaravilli, T, Martinian, L, Wood, N, Scaravilli, F, Ansorge, O

Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and Parkin-linked Parkinson's disease. by Hu, M, Scherfler, C, Khan, N, Hajnal, J, Lees, A, Quinn, N, Wood, N, Brooks, D

Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases. by Pang, J, Giunti, P, Chamberlain, S, An, S, Vitaliani, R, Scaravilli, T, Martinian, L, Wood, N, Scaravilli, F, Ansorge, O

Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease. by Lee, M, Nelson, I, Houlden, H, Sweeney, MG, Hilton-Jones, D, Blake, J, Wood, N, Reilly, M

Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin. by Tate, S, Depondt, C, Sisodiya, S, Cavalleri, G, Schorge, S, Soranzo, N, Thom, M, Sen, A, Shorvon, S, Sander, J, Wood, N, Goldstein, D

Alternative ion channel splicing in mesial temporal lobe epilepsy and Alzheimer's disease. by Heinzen, E, Yoon, W, Weale, M, Sen, A, Wood, N, Burke, JR, Welsh-Bohmer, K, Hulette, C, Sisodiya, S, Goldstein, D

Emergence of synaptic and cognitive impairment in a mature-onset APP mouse model of Alzheimer’s disease by Sri, S, Pegasiou, C, Cave, C, Hough, K, Wood, N, Gomez-Nicola, D, Deinhardt, K, Bannerman, D, Perry, V, Vargas-Caballero, M

Enhancing current guidance for psoriatic arthritis and its comorbidities: recommendations from an expert consensus panel by Coates, LC, Bukhari, M, Chan, A, Choy, E, Galloway, J, Gullick, N, Kent, A, Savage, L, Siebert, S, Tillett, W, Wood, N, Conaghan, PG

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease by Neumann, J, Bras, J, Deas, E, O'Sullivan, S, Parkkinen, L, Lachmann, R, Li, A, Holton, J, Guerreiro, R, Paudel, R, Segarane, B, Singleton, A, Lees, A, Hardy, J, Houlden, H, Revesz, T, Wood, N