UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Browse by UCL Departments and Centres

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Author | Type
Jump to: A | B | C | D | E | F | G | H | J | K | L | M | N | O | P | Q | R | S | T | V | W | Z
Number of items: 103.


Alarcon, F; Duenas, G; Cevallos, N; Lees, AJ; (2000) Movement disorders in 30 patients with tuberculous meningitis. MOVEMENT DISORD , 15 (3) 561 - 569.

Annaert, W; Cupers, P; Saftig, P; De Strooper, B; (2000) Presenilin function in APP processing. Ann N Y Acad Sci , 920 pp. 158-164.

Annaert, W; De Strooper, B; (2000) Neuronal models to study amyloid precursor protein expression and processing in vitro. Biochim Biophys Acta , 1502 (1) pp. 53-62.


Baekelandt, V; Claeys, A; Cherepanov, P; De Clercq, E; De Strooper, B; Nuttin, B; Debyser, Z; (2000) DNA-Dependent protein kinase is not required for efficient lentivirus integration. J Virol , 74 (23) pp. 11278-11285.

Baekelandt, V; De Strooper, B; Nuttin, B; Debyser, Z; (2000) Gene therapeutic strategies for neurodegenerative diseases. Curr Opin Mol Ther , 2 (5) pp. 540-554.

Baker, M; Graff-Radford, D; Wavrant DeVrièze, F; Graff-Radford, N; Petersen, RC; Kokmen, E; Boeve, B; (2000) No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease. Neurosci Lett , 285 (2) pp. 147-149.

Bandmann, O; Vaughan, JR; Holmans, P; Marsden, CD; Wood, NW; (2000) Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease. MOVEMENT DISORD , 15 (1) 30 - 35.

Benamer, HTS; Patterson, J; Grosset, DG; Booij, J; de Bruin, K; van Royen, E; Speelman, JD; (2000) Accurate differentiation of parkinsonism and essential tremor using visual assessment of [I-123]-FP-CIT SPECT imaging: The [I-123]-FP-CIT study group. MOVEMENT DISORD , 15 (3) 503 - 510.

Benamer, TS; Patterson, J; Grosset, DG; Booij, J; de Bruin, K; van Royen, E; Speelman, JD; (2000) Accurate differentiation of parkinsonism and essential tremor using visual assessment of [123I]-FP-CIT SPECT imaging: the [123I]-FP-CIT study group. Mov Disord , 15 (3) pp. 503-510.


Carmichael, J; Conron, M; Beynon, H; Crow, J; Warner, TT; (2000) Churg-Strauss syndrome presenting with visual loss. RHEUMATOLOGY , 39 (12) 1433 - 1434.

Chawda, SJ; Munchau, A; Johnson, D; Bhatia, K; Quinn, NP; Stevens, J; Lees, AJ; (2000) Pattern of premature degenerative changes of the cervical spine in patients with spasmodic torticollis and the impact on the outcome of selective peripheral denervation. J NEUROL NEUROSUR PS , 68 (4) 465 - 471.

Cottrell, DA; Blakely, EL; Johnson, MA; Chinnery, PF; Hanna, M; Turnbull, DM; (2000) Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorder. J NEUROPATH EXP NEUR , 59 (7) 621 - 627.


Davies, NP; Eunson, LH; Gregory, RP; Mills, KR; Morrison, PJ; Hanna, MG; (2000) Clinical, electrophysiological, and molecular genetic studies in a new family with paramyotonia congenita. J NEUROL NEUROSUR PS , 68 (4) 504 - 507.

De Strooper, B; (2000) Alzheimer's disease. Closing in on gamma-secretase. Nature , 405 (6787) pp. 627-629. 10.1038/35015193.

De Strooper, B; Annaert, W; (2000) Proteolytic processing and cell biological functions of the amyloid precursor protein. J Cell Sci , 113 ( pp. 1857-1870.

Doder, M; Rabiner, EA; Turjanski, N; Lees, AJ; Brooks, DJ; (2000) Imaging serotonin HT1A binding in non-depressed and depressed Parkinson's disease patients with C-11-WAY100635 PET. NEUROLOGY , 54 (7) A112 - A112.

de Silva, HA; Khan, NL; Wood, NW; (2000) The genetics of Parkinson's disease. CURR OPIN GENET DEV , 10 (3) 292 - 298.


Elson, GCA; Lelievre, E; Guillet, C; Chevalier, S; Plun-Favreau, H; Froger, J; Suard, I; (2000) CLF associates with CLC to form a functional heteromeric ligand for the CNTF receptor complex. NAT NEUROSCI , 3 (9) 867 - 872.

Eunson, LH; Rea, R; Zuberi, SM; Youroukos, S; Panayiotopoulos, CP; Liguori, R; Avoni, P; (2000) Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability. ANN NEUROL , 48 (4) 647 - 656.


Farrer, M; Destée, T; Becquet, E; Wavrant-De Vrièze, F; Mouroux, V; Richard, F; Defebvre, L; (2000) Linkage exclusion in French families with probable Parkinson' s disease. Mov Disord , 15 (6) pp. 1075-1083.


Geddes, JF; Jansen, GH; Robinson, SFD; Gomori, E; Holton, JL; Monson, JP; Besser, GM; (2000) 'Gangliocytomas' of the pituitary - A heterogeneous group of lesions with differing histogenesis. AM J SURG PATHOL , 24 (4) 607 - 613.

Ghiso, J; Vidal, R; Rostagno, A; Miravalle, L; Holton, JL; Mead, S; Revesz, T; (2000) Amyloidogenesis in familial British dementia is associated with a genetic defect on chromosome 13. MOLECULAR BASIS OF DEMENTIA , 920 84 - 92.

Giovannoni, G; Lees, AJ; (2000) Hedonistic homeostatic dysregulation in patients with Parkinson's disease on dopamine replacement therapies - Reply. J NEUROL NEUROSUR PS , 69 (4) p. 567.

Giovannoni, G; O'Sullivan, JD; Turner, K; Manson, AJ; Lees, AJL; (2000) Hedonistic homeostatic dysregulation in patients with Parkinson's disease on dopamine replacement therapies. J NEUROL NEUROSUR PS , 68 (4) 423 - 428.

Gwinn-Hardy, K; Chen, JY; Liu, HC; Liu, TY; Boss, M; Seltzer, W; Adam, A; (2000) Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese. Neurology , 55 (6) pp. 800-805.

Gwinn-Hardy, K; Mehta, ND; Farrer, M; Maraganore, D; Muenter, M; Yen, SH; Hardy, J; (2000) Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p. Acta Neuropathol , 99 (6) pp. 663-672.

Gwinn-Hardy, KA; Crook, R; Lincoln, S; Adler, CH; Caviness, JN; Hardy, J; Farrer, M; (2000) A kindred with Parkinson's disease not showing genetic linkage to established loci. Neurology , 54 (2) pp. 504-507.


Hardy, J; (2000) Pathways to primary neurodegenerative disease. Presented at: UNSPECIFIED, United States.

Hardy, J; Singleton, A; (2000) The future of genetic analysis of neurological disorders. Neurobiol Dis , 7 (2) pp. 65-69. 10.1006/nbdi.2000.0291.

Herreman, A; Serneels, L; Annaert, W; Collen, D; Schoonjans, L; De Strooper, B; (2000) Total inactivation of gamma-secretase activity in presenilin-deficient embryonic stem cells. Nat Cell Biol , 2 (7) pp. 461-462. 10.1038/35017105.

Holton, JL; Lashley, T; Vidal, R; Rostagno, A; Guerin, CJ; Houlden, H; Plant, G; (2000) Familial British dementia: Immunohistochemical and immunoelectron microscopic study. BRAIN PATHOL , 10 (4) 713 - 714.

Holton, JL; Steel, T; Luxsuwong, M; Crockard, HA; Revesz, T; (2000) Skull base chordomas: correlation of tumour doubling time with age, mitosis and Ki67 proliferation index. NEUROPATH APPL NEURO , 26 (6) 497 - 503.

Houlden, H; Baker, M; Bhatia, K; Hutton, M; Wood, N; Corticobasal Degeneration Collabor, ; (2000) Pathologically confirmed corticobasal degeneration shares the same tau haplotype association as progressive supranuclear palsy. ANN NEUROL , 48 (3) 436 - 436.

Houlden, H; Baker, M; McGowan, E; Lewis, P; Hutton, M; Crook, R; Wood, NW; (2000) Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations. ANN NEUROL , 48 (5) 806 - 808.

Houlden, H; Parlette, E; Dominguez, K; Hoffler, KD; Chui, CK; (2000) On the application of wavelet methods to simulation aerodynamic modeling. 21st Aerodynamic Measurement Technology and Ground Testing Conference


Jarman, PR; Bhatia, KP; Davie, C; Heales, SJR; Turjanski, N; Taylor-Robinson, SD; Marsden, CD; (2000) Paroxysmal dystonic choreoathetosis: Clinical features and investigation of pathophysiology in a large family. MOVEMENT DISORD , 15 (4) 648 - 657.

Jouvenceau, A; Eunson, L; Spauschus, A; Ramesh, V; Hanna, MG; Kullmann, DM; (2000) Non-functional alpha(1A) calcium channel in episodic ataxia type 2. J PHYSIOL-LONDON , 525 75P - 75P.

Jouvenceau, A; Eunson, L; Spauschus, A; Ramesh, V; Hanna, MG; Kullmann, DM; (2000) Premature termination in the CACNA1A gene observed in episodic ataxia type 2 (EA2) results in a loss of alpha1A calcium channel function. EUR J NEUROSCI , 12 454 - 454.


Kimber, J; Mathias, CJ; Lees, AJ; Bleasdale-Barr, K; Chang, HS; Churchyard, A; Watson, L; (2000) Physiological, pharmacological and neurohormonal assessment of autonomic function in progressive supranuclear palsy. BRAIN , 123 1422 - 1430.

Kingsbury, AE; Sangha, H; Eisen, S; Daniel, SE; Lees, AJ; Foster, OJF; (2000) Alteration in alpha synuclein gene transcription Parkinson's disease. EUR J NEUROSCI , 12 216 - 216.

Ko, L; Mehta, ND; Farrer, M; Easson, C; Hussey, J; Yen, S; Hardy, J; (2000) Sensitization of neuronal cells to oxidative stress with mutated human alpha-synuclein. J Neurochem , 75 (6) pp. 2546-2554.

Kumar-Singh, S; De Jonghe, C; Cruts, M; Kleinert, R; Wang, R; Mercken, M; De Strooper, B; (2000) Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's disease. Hum Mol Genet , 9 (18) pp. 2589-2598.


Lambert, JC; Goumidi, L; Vrièze, FW; Frigard, B; Harris, JM; Cummings, A; Coates, J; (2000) The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease. Hum Mol Genet , 9 (15) pp. 2275-2280.

Ledesma, MD; Da Silva, JS; Crassaerts, K; Delacourte, A; De Strooper, B; Dotti, CG; (2000) Brain plasmin enhances APP alpha-cleavage and Abeta degradation and is reduced in Alzheimer's disease brains. EMBO Rep , 1 (6) pp. 530-535. 10.1093/embo-reports/kvd107.

Lees, AJ; Lang, AE; (2000) Tremor - Basic mechanisms and clinical aspects - A symposium of the Movement Disorder Society held in Kiel, Germany, on July 11-12, 1997. MOVEMENT DISORDERS , 15 (1) 1 - 1.

Lewis, J; McGowan, E; Rockwood, J; Melrose, H; Nacharaju, P; Van Slegtenhorst, M; Gwinn-Hardy, K; (2000) Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein. Nat Genet , 25 (4) pp. 402-405. 10.1038/78078.

Lewis, PA; Perez-Tur, J; Golde, TE; Hardy, J; (2000) The presenilin 1 C92S mutation increases abeta 42 production. Biochem Biophys Res Commun , 277 (1) pp. 261-263. 10.1006/bbrc.2000.3646.

Lodi, R; Schapira, AHV; Manners, D; Styles, P; Wood, NW; Taylor, DJ; Warner, TT; (2000) Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy. ANN NEUROL , 48 (1) 72 - 76.

Lucking, CB; Durr, A; Bonifati, V; Vaughan, J; De Michele, G; Gasser, T; Harhangi, BS; (2000) Association between early-onset Parkinson's disease and mutations in the parkin gene. NEW ENGL J MED , 342 (21) 1560 - 1567.


Manson, AJ; Brown, P; O'Sullivan, JD; Asselman, P; Buckwell, D; Lees, AJ; (2000) An ambulatory dyskinesia monitor. J NEUROL NEUROSUR PS , 68 (2) 196 - 201.

Manson, AJ; Iakovidou, E; Lees, AJ; (2000) Idazoxan is ineffective for levodopa-induced dyskinesias in Parkinson's disease. MOVEMENT DISORD , 15 (2) 336 - 337.

Manson, AJ; Lees, AJ; (2000) Apomorphine therapy in Parkinson's disease: Clinical neuropharmacology and practical use. In: 5TH CONGRESS OF THE EUROPEAN SOCIETY FOR CLINICAL NEUROPHARMACOLOGY. (pp. 25 - 31).

Manson, AJ; Schrag, A; Lees, AJ; (2000) Low-dose olanzapine for levodopa induced dyskinesias. NEUROLOGY , 55 (6) 795 - 799.

Maraganore, DM; Farrer, MJ; Hardy, JA; McDonnell, SK; Schaid, DJ; Rocca, WA; (2000) Case-control study of debrisoquine 4-hydroxylase, N-acetyltransferase 2, and apolipoprotein E gene polymorphisms in Parkinson's disease. Mov Disord , 15 (4) pp. 714-719.

McEntagart, M; Norton, N; Williams, H; Houlden, H; Donaghy, M; Boltshauser, E; Harper, PS; (2000) Localisation of the gene for distal Hereditary Motor Neuronopathy-VII to chromosome 2. J MED GENET , 37 S85 - S85.

McEntagart, ME; Norton, N; Williams, H; Houlden, H; Boltshauser, E; Donaghy, M; Harper, PS; (2000) Localization of the gene for distal Hereditary Motor Neuronopathy-VII to chromosome 2. AM J HUM GENET , 67 (4) 311 - 311.

Meschia, JF; Brott, TG; Chukwudelunzu, FE; Hardy, J; Brown, RD; Meissner, I; Hall, LJ; (2000) Verifying the stroke-free phenotype by structured telephone interview. STROKE , 31 (5) pp. 1076-1080.

Morgan, D; Diamond, DM; Gottschall, PE; Ugen, KE; Dickey, C; Hardy, J; Duff, K; (2000) A beta peptide vaccination prevents memory loss in an animal model of Alzheimer's disease. Nature , 408 (6815) pp. 982-985. 10.1038/35050116.

Morris, HR; Lees, AJ; (2000) Parkinsonism following electrical injury to the hand - Reply. MOVEMENT DISORDERS , 15 (3) 587 - 588. 10.1002/1531-8257(200005)15:3<587::AID-MDS1028>3.0.CO;2-O.

Morris, HR; Thacker, AJ; Newman, PK; Lees, AJ; (2000) Sign language tics in a prelingually deaf man. MOVEMENT DISORD , 15 (2) 318 - 320.

Morris, HR; Vaughan, JR; Datta, SR; Bandopadhyay, R; de Silva, HAR; Schrag, A; Cairns, NJ; (2000) Multiple system atrophy/progressive supranuclear palsy: alpha-Synuclein, synphilin, tau, and APOE. NEUROLOGY , 55 (12) 1918 - 1920.

Munchau, A; Valente, EM; Davis, MB; Stinton, V; Wood, NW; Quinn, NP; Bhatia, KP; (2000) A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia. MOVEMENT DISORD , 15 (5) 954 - 959.

Munchau, A; Valente, EM; Shahidi, GA; Eunson, LH; Hanna, RG; Quinn, NP; Schapira, AHV; (2000) A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study. J NEUROL NEUROSUR PS , 68 (5) 609 - 614.

Myers, A; Holmans, P; Marshall, H; Kwon, J; Meyer, D; Ramic, D; Shears, S; (2000) Susceptibility locus for Alzheimer's disease on chromosome 10. Science , 290 (5500) pp. 2304-2305. 10.1126/science.290.5500.2304.

Myllykangas, L; Polvikoski, T; Sulkava, R; Verkkoniemi, A; Tienari, P; Niinistö, L; Kontula, K; (2000) Cardiovascular risk factors and Alzheimer's disease: a genetic association study in a population aged 85 or over. Neurosci Lett , 292 (3) pp. 195-198.


Nath, U; Morris, H; Thomson, R; Ben-Shlomo, Y; Wood, N; Lees, A; Burn, DJ; (2000) Prevalence of progressive supranuclear palsy (PSP) (Steele-Richardson-Olszewski syndrome) in the United Kingdom and creation of a national register. NEUROLOGY , 54 (7) A393 - A393.


O'Sullivan, JD; Bhatia, KP; Lees, AJ; (2000) Botulinum toxin A as treatment for drooling saliva in PD. NEUROLOGY , 55 (4) 606 - 607.

O'Sullivan, JD; Bhatia, KP; Lees, AJ; (2000) Botulinum toxin A as treatment for drooling saliva in PD. Neurology , 55 (4) pp. 606-7.

O'Sullivan, JD; Hanagasi, HA; Daniel, SE; Tidswell, P; Davies, SW; Lees, AJ; (2000) Neuronal intranuclear inclusion disease and juvenile parkinsonism. Mov Disord , 15 (5) pp. 990-995.

O'Sullivan, JD; Lees, AJ; (2000) Nonparkinsonian tremors. CLINICAL NEUROPHARMACOLOGY , 23 (5) 233 - 238.

Ostrerova-Golts, N; Petrucelli, L; Hardy, J; Lee, JM; Farer, M; Wolozin, B; (2000) The A53T alpha-synuclein mutation increases iron-dependent aggregation and toxicity. JOURNAL OF NEUROSCIENCE , 20 (16) 6048 - 6054. Green open access


Pickering-Brown, S; Baker, M; Yen, SH; Liu, WK; Hasegawa, M; Cairns, N; Lantos, PL; (2000) Pick's disease is associated with mutations in the tau gene. ANN NEUROL , 48 (6) 859 - 867.

Pulkes, T; Eunson, L; Patterson, V; Siddiqui, A; Wood, NW; Nelson, IP; Morgan-Hughes, JA; (2000) Erratum: (Annals of Neurology (1999) 46 (916-919)). Annals of Neurology , 47 (6) 841-.

Pulkes, T; Siddiqui, A; Morgan-Hughes, JA; Hanna, MG; (2000) A novel mutation in the mitochondrial tRNA(Tyr) gene associated with exercise intolerance. NEUROLOGY , 55 (8) 1210 - 1212.

Pulkes, T; Sweeney, MG; Hanna, MG; (2000) Increased risk of stroke in patients with the A12308G polymorphism in mitochondria. LANCET , 356 (9247) 2068 - 2069.

Pulkes, T; Wills, AJ; Hanna, MG; (2000) Exercise intolerance associated with a novel stop codon mutation in the mitochondrial ND2 gene. ANNALS OF NEUROLOGY , 48 (3) 469 - 469.


Quinn, N; Maraganore, D; Morris, HR; Lees, AJ; (2000) Parkinsonism following electrical injury to the hand (multiple letters). Movement Disorders , 15 (3) pp. 587-588.


Rahman, S; Lake, BD; Taanman, JW; Hanna, MG; Cooper, JM; Schapira, AHV; Leonard, JV; (2000) Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms. BRAIN , 123 591 - 600.

Rea, R; Spauschus, A; Eunson, L; Hanna, MG; Kullmann, DM; (2000) Functional analysis of interactions between wild-type and mutant subunits of hKv1.1 in episodic ataxia type 1. J PHYSIOL-LONDON , 525 76P - 76P.

Revesz, T; Houlden, H; Holton, JL; Baker, M; Vowles, GH; Lashley, T; Wood, NW; (2000) Alzheimer's disease with spastic paraparesis due to deletion of exon 4 and a P436E point mutation of exon 12 of the presenilin 1 gene. BRAIN PATHOL , 10 (4) 633 - 633.

Rojo, A; Pernaute, RS; Fontan, A; Ruiz, PG; Honnorat, J; Lynch, T; Chin, S; (2000) Clinical genetics of familial progressive supranuclear palsy. BRAIN , 123 p. 419.


Scaravilli, F; Cordery, RJ; Kretzschmar, H; Gambetti, P; Brink, B; Fritz, V; Temlett, J; (2000) Sporadic fatal insomnia: A case study. ANN NEUROL , 48 (4) 665 - 668.

Scaravilli, F; Kretschmar, H; Gambetti, P; Brink, B; An, SF; Schulz-Schaeffer, WJ; Rossor, MN; (2000) Sporadic fatal insomnia (sFI): Report of a case. J NEUROPATH EXP NEUR , 59 (5) 433 - 433.

Scaravilli, T; Pramstaller, PP; Salerno, A; Egarter-Vigl, E; Giometto, B; Vitaliani, R; An, SF; (2000) Neuronal loss in Onuf's nucleus in three patients with progressive supranuclear palsy. ANN NEUROL , 48 (1) 97 - 101.

Schrag, A; Good, CD; Miszkiel, K; Morris, HR; Mathias, CJ; Lees, AJ; Quinn, NP; (2000) Differentiation of atypical parkinsonian syndromes with routine MRI. NEUROLOGY , 54 (3) 697 - 702.

Spauschus, A; Rea, R; Eunson, L; Hanna, MG; Kullmann, DM; (2000) Mutations of Kv1.1 found in patients with episodic ataxia type 1 (EA1) affect the open probability of channels in vitro. EUR J NEUROSCI , 12 25 - 25.

Spauschus, A; Rea, R; Eunson, L; Wood, NW; Hanna, MG; Kullmann, DM; (2000) Functional characterisation of mutant Kv1.1 subunits from two families with episodic ataxia type 1. J PHYSIOL-LONDON , 523 156P - 157P.

Steiner, H; Kostka, M; Romig, H; Basset, G; Pesold, B; Hardy, J; Capell, A; (2000) Glycine 384 is required for presenilin-1 function and is conserved in bacterial polytopic aspartyl proteases. Nat Cell Biol , 2 (11) pp. 848-851. 10.1038/35041097.


Tabrizi, SJ; Orth, M; Wilkinson, JM; Taanman, JW; Warner, TT; Cooper, JM; Schapira, AHV; (2000) Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicity. HUM MOL GENET , 9 (18) 2683 - 2689.

Tanaka, M; Endo, K; Suzuki, T; Kakita, A; Takahashi, H; Sata, T; (2000) Parkinsonism in HIV encephalopathy. Mov Disord , 15 (5) pp. 1032-1033.

Thom, M; Holton, JL; D'Arrigo, C; Griffin, B; Beckett, A; Sisodiya, S; Alexiou, D; (2000) Microdysgenesis with abnormal cortical myelinated fibres in temporal lobe epilepsy: a histopathological study with calbindin D-28-K immunohistochemistry. NEUROPATH APPL NEURO , 26 (3) 251 - 257.


Valente, EM; Spacey, SD; Wali, GM; Bhatia, KP; Dixon, PH; Wood, NW; Davis, MB; (2000) A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16. BRAIN , 123 2040 - 2045.

Verkkoniemi, A; Somer, M; Rinne, JO; Myllykangas, L; Crook, R; Hardy, J; Viitanen, M; (2000) Variant Alzheimer's disease with spastic paraparesis: clinical characterization. Neurology , 54 (5) pp. 1103-1109.

Vidal, R; Revesz, T; Rostagno, A; Kim, E; Holton, JL; Bek, T; Bojsen-Moller, M; (2000) A decamer duplication in the 3 ' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred. P NATL ACAD SCI USA , 97 (9) 4920 - 4925.


Warner, T; Camfield, L; Marsden, CD; Nemeth, AH; Hyman, N; Harley, D; Wissel, J; (2000) A prevalence study of primary dystonia in eight European countries. JOURNAL OF NEUROLOGY , 247 (10) pp. 787-792.

Weiler, M; de Silva, HAR; Morris, H; Wood, NW; Lees, AJ; (2000) Strong association of novel tau promoter polymorphisms with progressive supranuclear palsy. AM J HUM GENET , 67 (4) 193 - 193.

Wenning, GK; Ben-Shlomo, Y; Hughes, A; Daniel, SE; Lees, A; Quinn, NP; (2000) What clinical features are most useful to distinguish definite multiple system atrophy from Parkinson's disease? J NEUROL NEUROSUR PS , 68 (4) 434 - 440.

Wilson, CJ; Wood, NW; Leonard, JV; Surtees, R; Rahman, S; (2000) Mitochondrial DNA point mutation T9176C in Leigh syndrome. J CHILD NEUROL , 15 (12) 830 - 833.

Wood, NW; Harding, AE; (2000) Ataxic disorders. In: Bradley, WG and Daroff, RB and Fenichel, GM and Marsden, CD, (eds.) Neurology in clinical practice: volume 1. Principles of diagnosis and management. (pp. 309-317). Butterworth Heinemann: Oxford.

Wood, NW; Harding, AE; (2000) Cerebellar and spinocerebellar disorders. In: Bradley, WG and Daroff, RB and Fenichel, GM and Marsden, CD, (eds.) Neurology in clinical practice: volume 2. The neurological disorders. (pp. 1931-1951). Butterworth Heinemann: Oxford.

Worth, PF; Houlden, H; Giunti, P; Davis, MB; Wood, NW; (2000) Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia. NAT GENET , 24 (3) 214 - 215.

Worth, PF; Houlden, H; Giunti, P; Davis, MB; Wood, NW; Moseley, ML; Schut, LJ; (2000) Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia [2] (multiple letters). Nature Genetics , 24 (3) pp. 214-215. 10.1038/73411.


Zhang, J; Hattori, N; Leroy, E; Morris, HR; Kubo, SI; Kobayashi, T; Wood, NW; (2000) Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease. PARKINSONISM RELAT D , 6 (4) 195 - 197.

This list was generated on Sun Feb 7 03:17:26 2016 GMT.