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Number of items: 168.

A

Abou-Sleiman, PM; Healy, DG; Ahmadi, K; Goldstein, DB; Wood, NW; (2003) Population genetic approaches to Parkinsons disease. In: AMERICAN JOURNAL OF HUMAN GENETICS. (pp. 541 - 541). UNIV CHICAGO PRESS

Abou-Sleiman, PM; Healy, DG; Quinn, N; Lees, AJ; Wood, NW; (2003) The role of pathogenic DJ-1 mutations in Parkinson's disease. ANN NEUROL , 54 (3) 283 - 286. 10.1002/ana.10675.

Abramov, A.Y.; Canevari, L.; Duchen, M.R.; (2003) Changes in intracellular calcium and glutathione in astrocytes as the primary mechanism of amyloid neurotoxicity. Nature Chemical Biology , 23 (12) pp. 5088-5095. Green open access
file

Abramov, AY; Canevari, L; Duchen, MR; (2003) Amyloid beta peptide causes [Ca2+](c) fluctuations and decreases [GSH] in rat astrocytes. In: BIOPHYSICAL JOURNAL. (pp. 389A - 389A). BIOPHYSICAL SOCIETY

Abramov, AY; Canevari, L; Duchen, MR; (2003) Changes in intracellular calcium and glutathione in astrocytes as the primary mechanism of amyloid neurotoxicity. J NEUROSCI , 23 (12) 5088 - 5095.

Abramov, AY; Duchen, MR; (2003) Actions of ionomycin, 4-BrA23187 and a novel electrogenic Ca2+ ionophore on mitochondria in intact cells. CELL CALCIUM , 33 (2) 101 - 112.

Ahmad-Annuar, A; Shah, P; Hafezparast, M; Hummerich, H; Witherden, AS; Morrison, KE; Shaw, PJ; ... Fisher, EMC; + view all (2003) No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders. AMYOTROPH LATERAL SC , 4 (3) 150 - 157.

Alves, JD; Ames, PRJ; Donohue, S; Stanyer, L; Nourooz-Zadeh, J; Ravirajan, C; Isenberg, DA; (2003) Antibodies to high-density lipoprotein and beta(2)-glycoprotein I are inversely correlated with paraoxonase activity in systematic lupus erythematosus (vol 46, pg 2686, 2002). ARTHRITIS RHEUM , 48 (1) 284 - 284. 10.1002/art.539.

Andorfer, C; Kress, Y; Espinoza, M; de Silva, R; Tucker, KL; Barde, YA; Duff, K; (2003) Hyperphosphorylation and aggregation of tau in mice expressing normal human tau isoforms. J NEUROCHEM , 86 (3) 582 - 590. 10.1046/j.1471-4159.2003.01879.x.

B

Baptista, MJ; O'Farrell, C; Daya, S; Ahmad, R; Miller, DW; Hardy, J; Farrer, MJ; (2003) Co-ordinate transcriptional regulation of dopamine synthesis genes by alpha-synuclein in human neuroblastoma cell lines. JOURNAL OF NEUROCHEMISTRY , 85 (4) pp. 957-968. 10.1046/j.1471-4159.2003.01742.x.

Baptista, MJ; O'Farrell, C; Hardy, J; Cookson, MR; (2003) Microarray analysis reveals induction of heat shock proteins mRNAs by the torsion dystonia protein, TorsinA. NEUROSCIENCE LETTERS , 343 (1) pp. 5-8. 10.1016/S0304-3940(03)00302-1.

Baumann, M; Mamais, A; McBlane, F; Xiao, H; Boyes, J; (2003) Regulation of V(D)J recombination by nucleosome positioning at recombination signal sequences. EMBO J , 22 (19) 5197 - 5207.

Borestrom, C; Zetterberg, H; Liff, K; Rymo, L; (2003) Functional interaction of nuclear factor Y and Sp1 is required for activation of the Epstein-Barr virus C promoter. JOURNAL OF VIROLOGY , 77 (2) pp. 821-829. 10.1128/JVI.77.2.821-829.2003.

Brancati, F; Valente, EM; Davies, NP; Sarkozy, A; Sweeney, MG; LoMonaco, M; Pizzuti, A; ... Dallapiccola, B; + view all (2003) Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A. J NEUROL NEUROSUR PS , 74 (9) 1339 - 1341.

Broomand, A; Mannikko, R; Larsson, HP; Elinder, F; (2003) Molecular movement of the voltage sensor in a K channel. JOURNAL OF GENERAL PHYSIOLOGY , 122 (6) pp. 741-748. 10.1085/jgp.200308927.

C

Cairns, NJ; Perry, RH; Jaros, E; Burn, D; McKeith, IG; Lowe, JS; Holton, J; ... Lantos, PL; + view all (2003) Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions. NEUROSCI LETT , 341 (3) 177 - 180. 10.1016/S0304-3940(03)00100-9.

Cheung, KK; Ryten, M; Burnstock, G; (2003) Abundant and dynamic expression of G protein-coupled P2Y receptors in mammalian development. Developmental Dynamics , 228 (2) pp. 254-266. 10.1002/dvdy.10378.

Cheung, KK; Ryten, M; Burnstock, G; (2003) Abundant and dynamic expression of G protein-coupled P2Y receptors in mammalian development. DEVELOPMENTAL DYNAMICS , 228 (2) pp. 254-266. 10.1002/dvdy.10378.

Church, AJ; Dale, RC; Cardoso, F; Candler, PM; Chapman, MD; Allen, ML; Klein, NJ; ... Giovannoni, G; + view all (2003) CSF and serum immune parameters in Sydenham's chorea: evidence of an autoimmune syndrome? J NEUROIMMUNOL , 136 (1-2) 149 - 153. 10.1016/S0165-5728(03)00012-2.

Church, AJ; Dale, RC; Lees, AJ; Giovannoni, G; Robertson, MM; (2003) Tourette's syndrome: a cross sectional study to examine the PANDAS hypothesis. J NEUROL NEUROSUR PS , 74 (5) 602 - 607.

Colosimo, C; Hughes, AJ; Kilford, L; Lees, AJ; (2003) Lewy body cortical involvement may not always predict dementia in Parkinson's disease. J NEUROL NEUROSUR PS , 74 (7) 852 - 856.

Colosimo, C; Osaki, Y; Vanacore, N; Lees, AJ; (2003) Lack of association between progressive supranuclear palsy and arterial hypertension: a clinicopathological study. Mov Disord , 18 (6) pp. 694-697. 10.1002/mds.10392.

Cordivari, C; Vincent, A; Misra, VP; Catania, S; Murray, NMF; Bhatia, KP; Lees, AJ; (2003) Failure to identify change in the cervical dystonia muscle pattern is the main cause of reduced response to BTXA. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 408 - 409). BRITISH MED JOURNAL PUBL GROUP

D

Dabrowski, M; Aerts, S; Van Hummelen, P; Craessaerts, K; De Moor, B; Annaert, W; Moreau, Y; (2003) Gene profiling of hippocampal neuronal culture. JOURNAL OF NEUROCHEMISTRY , 85 (5) pp. 1279-1288. 10.1046/j.1471-4159.2003.01753.x.

Davies, NA; Cochrane, G; Hanna, M; (2003) Muscle disorders. In: Greenwood, RJ and Barnes, MP and McMillan, TM and Ward, CD, (eds.) Handbook of neurological rehabilitation. (pp. 705-725). Psychology Press: Hove.

Davies, NP; Hanna, MG; (2003) The skeletal muscle channelopathies: distinct entities and overlapping syndromes. CURR OPIN NEUROL , 16 (5) 559 - 568. 10.1097/01.wco.0000093098.34793.09.

De Strooper, B; (2003) Aph-1, Pen-2, and nicastrin with presenilin generate an active gamma-secretase complex. NEURON , 38 (1) pp. 9-12. 10.1016/S0896-6273(03)00205-8.

De Strooper, B; Woodgett, J; (2003) Alzheimer's disease - Mental plaque removal. NATURE , 423 (6938) pp. 392-393. 10.1038/423392a.

Doder, M; Rabiner, EA; Turjanski, N; Lees, AJ; Brooks, DJ; (2003) Tremor in Parkinson's disease and serotonergic dysfunction - An (11)C-WAY 100635 PET study. NEUROLOGY , 60 (4) pp. 601-605.

de Silva, R; Hope, A; Pittman, A; Weale, ME; Morris, HR; Wood, NW; Lees, AJ; (2003) Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy. NEUROLOGY , 61 (3) 407 - 409.

de Silva, R; Lashley, T; Gibb, G; Hanger, D; Hope, A; Reid, A; Bandopadhyay, R; ... Lees, A; + view all (2003) Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies. NEUROPATH APPL NEURO , 29 (3) 288 - 302.

de Silva, R.; Lashley, T.; Gibb, G.; Hanger, D.; Hope, A.; Reid, A.; Bandopadhyay, R.; ... Lees, A.; + view all (2003) Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies. Neuropathology and Applied Neurobiology , 29 (3) pp. 288-302. 10.1046/j.1365-2990.2003.00463.x.

E

Edwards, M; Wood, N; Bhatia, K; (2003) Unusual phenotypes in DYT1 dystonia: A report of five cases and a review of the literature. MOVEMENT DISORD , 18 (6) 706 - 711. 10.1002/mds.10411.

Edwards, M; Wood, N; Bhatia, K; (2003) Unusual phenotypes in DYT1 dystonia: A report of five cases and a review of the literature. Movement Disorders , 18 (6) pp. 706-711. 10.1002/mds.10411.

Edwards, M.J.; Huang, Y.-Z.; Wood, N.W.; Rothwell, J.C.; Bhatia, K.P.; (2003) Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation. Brain , 126 (9) pp. 2074-2080. 10.1093/brain/awg209.

Edwards, MJ; Huang, YZ; Wood, NW; Rothwell, JC; Bhatia, KP; (2003) Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation. BRAIN , 126 2074 - 2080. 10.1093/brain/awg209.

Eerola, J; Hernandez, D; Launes, J; Hellstrom, O; Hague, S; Gulick, C; Johnson, J; ... Singleton, AB; + view all (2003) Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD. NEUROLOGY , 61 (7) pp. 1000-1002.

Egorov, AV; Angelova, PR; Heinemann, U; Muller, W; (2003) Ca2+-independent muscarinic excitation of rat medial entorhinal cortex layer V neurons. EUROPEAN JOURNAL OF NEUROSCIENCE , 18 (12) pp. 3343-3351. 10.1046/j.1460-9568.2003.03050.x.

El-Agnaf, OMA; Salem, SA; Paleologou, KE; Cooper, LJ; Fullwood, NJ; Gibson, MJ; Curran, MD; ... Allsop, D; + view all (2003) alpha-synuclein implicated in Parkinson's disease is present in extracellular biological fluids, including human plasma. FASEB JOURNAL , 17 (11) 1945-+. 10.1096/fj.03-0098fje.

Emre, M; Lees, AJ; (2003) Parkinsonism and dementia: Synucleinopathies, tauopathies and beyond - Introduction. MOVEMENT DISORDERS , 18 S1-S1. 10.1002/mds.10556.

F

Frank, RA; Galasko, D; Hampel, H; Hardy, J; de Leon, MJ; Mehta, PD; Rogers, J; ... National Institute on Aging Biological Markers Working Group, ; + view all (2003) Biological markers for therapeutic trials in Alzheimer's disease. Proceedings of the biological markers working group; NIA initiative on neuroimaging in Alzheimer's disease. Neurobiol Aging , 24 (4) pp. 521-536.

G

GEWINNER, C; Mueller, CW; Soler-Lopez, M; Groner, B; (2003) Signal transducers and activators of transcription (STATs): Activation and Biology. [Book]. X-ray cristal structure of Stat proteins and structure activity relationship. (1st ed.). Springer

Gasser, T; Wood, NW; (2003) Molecular Genetic Diagnosis of Neurological Diseases. In: Neurological Disorders: Course and Treatment: Second Edition. (pp. 1525-1538).

Gerschlager, W; Katzenschlager, R; Schrag, A; Lees, AJ; Brown, P; Quinn, N; Bhatia, KP; (2003) Quality of life in patients with orthostatic tremor. J NEUROL , 250 (2) 212 - 215. 10.1007/s00415-003-0980-9.

Gibson, GE; Kingsbury, AE; Xu, H; Lindsay, JG; Daniel, S; Foster, OJF; Lees, AJ; (2003) Deficits in a tricarboxylic acid cycle enzyme in brains from patients with Parkinson's disease. Neurochem Int , 43 (2) pp. 129-135.

Goldstein, D.B.; Ahmadi, K.R.; Weale, M.E.; Wood, N.W.; (2003) Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. Trends in Genetics , 19 (11) pp. 615-622. 10.1016/j.tig.2003.09.006.

Goldstein, DB; Ahmadi, KR; Weale, ME; Wood, NW; (2003) Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. TRENDS GENET , 19 (11) 615 - 622. 10.1016/j.tig.2003.09.006.

Grover, A; England, E; Baker, M; Sahara, N; Adamson, J; Granger, B; Houlden, H; ... Hutton, M; + view all (2003) A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathy. EXP NEUROL , 184 (1) 131 - 140. 10.1016/S0014-4886(03)00393-5.

Groves, MJ; Schanzer, A; Simpson, AJ; An, SF; Kuo, LT; Scaravilli, F; (2003) Profile of adult rat sensory neuron loss, apoptosis and replacement after sciatic nerve crush. J NEUROCYTOL , 32 (2) 113 - 122.

H

Hadjivassiliou, M; Grunewald, R; Sharrack, B; Sanders, D; Lobo, A; Williamson, C; Woodroofe, N; ... Davies-Jones, A; + view all (2003) Gluten ataxia in perspective: epidemiology, genetic susceptibility and clinical characteristics. BRAIN , 126 685 - 691. 10.1093/brain/awg050.

Hague, S; Rogaeva, E; Hernandez, D; Gulick, C; Singleton, A; Hanson, M; Johnson, J; ... Singleton, A; + view all (2003) Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation. ANNALS OF NEUROLOGY , 54 (2) pp. 271-274. 10.1002/ana.10663.

Hardy, J; (2003) Alzheimer's disease: Genetic evidence points to a single pathogenesis. ANNALS OF NEUROLOGY , 54 (2) pp. 143-144. 10.1002/ana.10624.

Hardy, J; (2003) Impact of genetic analysis on Parkinson's disease research. In: MOVEMENT DISORDERS. (pp. S96 - S98). WILEY-LISS

Hardy, J; (2003) The relationship between Lewy body disease, Parkinson's disease, and Alzheimer's disease. Annals of the New York Academy of Sciences , 991 pp. 167-170.

Hardy, J; (2003) The relationship between amyloid and tau. JOURNAL OF MOLECULAR NEUROSCIENCE , 20 (2) pp. 203-206. 10.1385/JMN:20:2:203.

Hardy, J; Cookson, MR; Singleton, A; (2003) Genes and parkinsonism. LANCET NEUROLOGY , 2 (4) pp. 221-228. 10.1016/S1474-4422(03)00350-8.

Hardy, J; Singleton, A; Gwinn-Hardy, K; (2003) Ethnic differences and disease phenotypes. Science , 300 (5620) pp. 739-740. 10.1126/science.300.5620.739.

Hargreaves, IP; Heales, SJR; Briddon, A; Lee, PJ; Hanna, MG; Land, JM; (2003) Primary pyruvate dehydrogenase E3 binding protein deficiency with mild hyperlactataemia and hyperalaninaemia. J INHERIT METAB DIS , 26 (5) 505 - 506.

Harold, D; Peirce, T; Moskvina, V; Myers, A; Jones, S; Hollingworth, P; Moore, P; ... Jones, L; + view all (2003) Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease. HUMAN GENETICS , 113 (3) pp. 258-267. 10.1007/s00439-003-0960-2.

Hernandez, D; Hanson, M; Singleton, A; Gwinn-Hardy, K; Freeman, J; Ravina, B; Doheny, D; ... Singleton, A; + view all (2003) Mutation at the SCA17 locus is not a common cause of parkinsonism. PARKINSONISM & RELATED DISORDERS , 9 (6) pp. 317-320. 10.1016/S1353-8020(03)00027-0.

Herreman, A; Van Gassen, G; Bentahir, M; Nyabi, O; Craessaerts, K; Mueller, U; Annaert, W; (2003) γ-Secretase activity requires the presenilin-dependent trafficking of nicastrin through the Golgi apparatus but not its complex glycosylation. Journal of Cell Science , 116 (6) pp. 1127-1136. 10.1242/jcs.00292.

Herreman, A; Van Gassen, G; Bentahir, M; Nyabi, O; Craessaerts, K; Mueller, U; Annaert, W; (2003) gamma-Secretase activity requires the presenilin-dependent trafficking of nicastrin through the Golgi apparatus but not its complex glycosylation. JOURNAL OF CELL SCIENCE , 116 (6) pp. 1127-1136. 10.1242/jcs.00292.

Hogg, M; Grujic, ZM; Baker, M; Demirci, S; Guillozet, AL; Sweet, AP; Herzog, LL; ... Bigio, EH; + view all (2003) The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy. ACTA NEUROPATHOL , 106 (4) 323 - 336. 10.1007/s00401-003-0734-x.

Holton, JL; Beesley, C; Winchester, B; Al-Memar, A; (2003) Vacuolar myopathy in twin girls. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY , 29 (5) p. 525.

Hope, AD; de Silva, R; Fischer, DF; Hol, EM; van Leeuwen, FW; Lees, AJ; (2003) Alzheimer's associated variant ubiquitin causes inhibition of the 26S proteasome and chaperone expression. J NEUROCHEM , 86 (2) 394 - 404. 10.1046/j.1471-4159.2003.01844.x.

Houlden, H; Lincoln, S; Farrer, M; Cleland, PG; Hardy, J; Orrell, RW; (2003) Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic. NEUROLOGY , 61 (10) 1423 - 1426.

Houlden, H.; Lincoln, S.; Farrer, M.; Cleland, P.G.; Hardy, J.; Orrell, R.W.; (2003) Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic. Neurology , 61 (10) pp. 1423-1426.

I

Iseki, E; Togo, T; Suzuki, K; Katsuse, O; Marui, W; de Silva, R; Lees, A; ... Kosaka, K; + view all (2003) Dementia with Lewy bodies from the perspective of tauopathy. ACTA NEUROPATHOL , 105 (3) 265 - 270. 10.1007/s00401-002-0644-3.

J

Janssen, JC; Beck, JA; Campbell, TA; Dickinson, A; Fox, NC; Harvey, RJ; Houlden, H; ... Collinge, J; + view all (2003) Early onset familial Alzheimer's disease - Mutation frequency in 31 families. NEUROLOGY , 60 (2) 235 - 239.

Johansson, A; Hampel, H; Faltraco, F; Buerger, K; Minthon, L; Bogdanovic, N; Sjogren, M; ... Blennow, K; + view all (2003) Increased frequency of a new polymorphism in the cycle 2 (cdc2) gene in patients with Alzheimer's disease frontotemporal dementia. NEUROSCIENCE LETTERS , 340 (1) pp. 69-73. 10.1016/S0304-3940(03)00051-X.

Josephs, K.A.; Holton, J.L.; Rossor, M.N.; Braendgaard, H.; Ozawa, T.; Fox, N.C.; Petersen, R.C.; ... Revesz, T.; + view all (2003) Neurofilament inclusion body disease: a new proteinopathy? Brain , 126 (10) pp. 2291-2303. 10.1093/brain/awg231.

Josephs, KA; Holton, JL; Rossor, MN; Braendgaard, H; Ozawa, T; Fox, NC; Petersen, RC; ... Revesz, T; + view all (2003) Neurofilament inclusion body disease. In: ANNALS OF NEUROLOGY. (pp. S51 - S51). WILEY-LISS

Josephs, KA; Holton, JL; Rossor, MN; Braendgaard, H; Ozawa, T; Fox, NC; Petersen, RC; ... Revesz, T; + view all (2003) Neurofilament inclusion body disease: a new proteinopathy? BRAIN , 126 2291 - 2303. 10.1093/brain/awg231.

Josephs, KA; Holton, JL; Rossor, MN; Braendgaard, H; Petersen, RC; Pearl, GS; Ganguly, M; ... Revesz, T; + view all (2003) Neurofilament inclusion body disease: a new proteinopathy. NEUROPATH APPL NEURO , 29 (5) 521 - 521.

K

Kahle, PJ; De Strooper, B; (2003) Attack on amyloid. EMBO Rep , 4 (8) pp. 747-751. 10.1038/sj.embor.embor905.

Katsuse, O; Iseki, E; Arai, T; Akiyama, H; Togo, T; Uchikado, H; Kato, M; ... Kosaka, K; + view all (2003) 4-repeat tauopathy sharing pathological and biochemical features of corticobasal degeneration and progressive supranuclear palsy. ACTA NEUROPATHOL , 106 (3) 251 - 260. 10.1007/s00401-003-0728-8.

Katzenschlager, R; Cardozo, A; Cobo, MRA; Tolosa, E; Lees, AJ; (2003) Unclassifiable parkinsonism in two European tertiary referral centres for movement disorders. MOVEMENT DISORD , 18 (10) 1123 - 1131. 10.1002/mds.10523.

Katzenschlager, R; Costa, D; Gerschlager, W; O'Sullivan, J; Zijlmans, J; Gacinovic, S; Pirker, W; ... Brown, P; + view all (2003) Erratum: [<sup>12</sup>I]-FP-CIT-SPECT demonstrates dopaminergic deficit in orthostatic tremor (Annals of Neurology (2003) 53 (489-496)). Annals of Neurology , 54 (2) 278-. 10.1002/ana.10704.

Katzenschlager, R; Costa, D; Gerschlager, W; O'Sullivan, J; Zijlmans, J; Gacinovic, S; Pirker, W; ... Brown, P; + view all (2003) [I-123]-FP-CIT-SPECT demonstrates dopaminergic deficit in orthostatic tremor. ANN NEUROL , 53 (4) 489 - 496. 10.1002/ana.10475.

Katzenschlager, R; Costa, D; Gerschlager, W; O'Sullivan, J; Zijlmans, J; Gacinovic, S; Pirker, W; ... Brown, P; + view all (2003) [I-12]-FP-CIT-SPECT demonstrates dopaminergic deficit in orthostatic tremor. (vol 53, pg 489, 2003). ANNALS OF NEUROLOGY , 54 (2) p. 278.

Katzenschlager, R; Sampaio, C; Costa, J; Lees, A; (2003) Anticholinergics for symptomatic management of Parkinson's disease. Cochrane Database Syst Rev (2) CD003735-. 10.1002/14651858.CD003735.

Khan, N.L.; Graham, E.; Critchley, P.; Schrag, A.E.; Wood, N.W.; Lees, A.J.; Bhatia, K.P.; (2003) Parkin disease: a phenotypic study of a large case series. Brain , 126 (6) pp. 1279-1292. 10.1093/brain/awg142.

Khan, NL; Graham, E; Critchley, P; Schrag, AE; Wood, NW; Lees, AJ; Bhatia, KP; (2003) Parkin disease: a phenotypic study of a large case series. BRAIN , 126 1279 - 1292. 10.1093/brain/awg142.

Khan, NL; Wood, NW; Bhatia, KP; (2003) Autosomal recessive, DYT2-like primary torsion dystonia - A new family. NEUROLOGY , 61 (12) 1801 - 1803.

Kuo, L; Scaravilli, F; Groves, MJ; An, SF; (2003) Gene expression of neurotrophins and their receptors in the dorsal root ganglion after axotomy and systemic NT-3 treatment. In: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. (pp. 578 - 578). AMER ASSN NEUROPATHOLOGISTS INC

Kuoppamaki, M; Giunti, P; Quinn, N; Wood, NW; Bhatia, KP; (2003) Slowly progressive cerebellar ataxia and cervical dystonia: Clinical presentation of a new form of spinocerebellar ataxia? MOVEMENT DISORD , 18 (2) 200 - 206. 10.1002/mds.10308.

L

Lang, AE; (2003) Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look-alike? Mov Disord , 18 (3) pp. 351-352. 10.1002/mds.10367.

Lang, AE; Lees, AJ; (2003) Untitled. MOVEMENT DISORDERS , 18 (1) p. 1. 10.1002/mds.10410.

Lauwers, E; Debyser, Z; Van Dorpe, J; De Strooper, B; Nuttin, B; Baekelandt, V; (2003) Neuropathology and neurodegeneration in rodent brain induced by lentiviral vectormediated overexpression of alpha-synuclein. BRAIN PATHOLOGY , 13 (3) pp. 364-372.

Lawrence, AD; Evans, AH; Lees, AJ; (2003) Compulsive use of dopamine replacement therapy in Parkinson's disease: reward systems gone awry? LANCET NEUROL , 2 (10) 595 - 604.

Lee, M.-J.; Stephenson, D.A.; Groves, M.J.; Sweeney, M.G.; Davis, M.B.; An, S.-F.; Houlden, H.; ... Reilly, M.M.; + view all (2003) Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene. Human Molecular Genetics , 12 (15) pp. 1917-1925. 10.1093/hmg/ddg198.

Lee, MJ; Stephenson, DA; Groves, MJ; Sweeney, MG; Davis, MB; An, SF; Houlden, H; ... Reilly, MM; + view all (2003) Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene. HUM MOL GENET , 12 (15) 1917 - 1925. 10.1093/hmg/ddg198.

Lees, AJ; (2003) Parkinson's syndrome associated with neurofibrillary degeneration and tau pathologic findings. In: MOVEMENT DISORDERS. (pp. S28 - S33). WILEY-LISS

Lees, AJ; (2003) Parkinson's syndrome associated with neurofibrillary degeneration and tau pathologic findings. Mov Disord , 18 Sup S28-S33. 10.1002/mds.10560.

Lees, AJ; Grosset, DG; (2003) Dopamine transporter imaging. Movement Disorders , 18 (Suppl.) S1-S2.

Lees, AJ; Grosset, DG; (2003) Dopamine transporter imaging. Mov Disord , 18 Sup S1-S2. 10.1002/mds.10570.

Leigh, PN; Ludolph, AC; Payan, CAM; Graf, M; Lacomblez, L; Vidailhet, M; Landwehrmeyer, B; ... Grp, NNIPPSS; + view all (2003) Cross-sectional clinical description of a large prospective cohort of patients with progressive supranuclear palsy or multiple system atrophy: The NNIPPS project. In: (pp. S70-S71).

Lhatoo, SD; Perunovic, B; Love, S; Houlden, H; Campbell, MJ; (2003) Familial idiopathic brain calcification - A new and familial alpha-synucleinopathy? EUR NEUROL , 49 (4) 223 - 226. 10.1159/000070189.

Lichtenthaler, SF; Dominguez, D; Westmeyer, GG; Reiss, K; Haass, C; Saftig, P; De Strooper, B; (2003) The cell adhesion protein P-selectin glycoprotein ligand-1 is a substrate for the aspartyl protease BACE1. JOURNAL OF BIOLOGICAL CHEMISTRY , 278 (49) pp. 48713-48719. 10.1074/jbc.M303861200.

Lincoln, S; Wiley, J; Lynch, T; Langston, JW; Chen, R; Lang, A; Rogaeva, E; ... Farrer, M; + view all (2003) Parkin-proven disease - Common founders but divergent phenotypes. NEUROLOGY , 60 (10) pp. 1605-1610.

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