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Jump to: B | C | D | F | G | H | J | L | M | N | O | P | Q | R | S | T | W
Number of items: 45.

B

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.

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 Disorders , 15 (1) pp. 30-35. 10.1002/1531-8257(200001)15:1<30::AID-MDS1007>3.0.CO;2-V.

C

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.

D

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.

F

Farrer, M; Destee, T; Becquet, E; Wavrant-De Vrieze, F; Mouroux, V; Richard, F; Defebvre, L; ... Chartier-Harlin, MC; + view all (2000) Linkage exclusion in French families with probable Parkinson's disease. MOVEMENT DISORDERS , 15 (6) pp. 1075-1083. 10.1002/1531-8257(200011)15:6<1075::AID-MDS1004>3.0.CO;2-2.

G

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.

Giovannoni, G; Lees, AJ; (2000) Hedonistic homeostatic dysregulation in patients with Parkinson's disease on dopamine replacement therapies - Reply. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 69 (4) p. 567.

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. 10.1212/WNL.54.2.504.

H

Hanagasi, HA; Kaptanoglu, G; Sahin, HA; Emre, M; (2000) The use of NMDA antagonist memantine in drug-resistant dyskinesias resulting from L-dopa. MOVEMENT DISORDERS , 15 (5) pp. 1016-1017. 10.1002/1531-8257(200009)15:5<1016::AID-MDS1042>3.0.CO;2-J.

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

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

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; 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

J

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 Disorders , 15 (4) pp. 648-657. 10.1002/1531-8257(200007)15:4&lt;648::AID-MDS1008&gt;3.0.CO;2-T.

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.

L

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) p. 1.

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. Annals of Neurology , 48 (1) pp. 72-76. 10.1002/1531-8249(200007)48:1<72::AID-ANA11>3.3.CO;2-9.

M

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: (pp. pp. 25-31).

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. MOVEMENT DISORDERS , 15 (4) pp. 714-719. 10.1002/1531-8257(200007)15:4<714::AID-MDS1018>3.0.CO;2-3.

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

Morris, HR; Lees, AJ; (2000) Parkinsonism following electrical injury to the hand - Reply. MOVEMENT DISORDERS , 15 (3) pp. 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.

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.

Myllykangas, L; Polvikoski, T; Sulkava, R; Verkkoniemi, A; Tienari, P; Niinisto, L; Kontula, K; ... Perez-Tur, J; + view all (2000) Cardiovascular risk factors and Alzheimer's disease: a genetic association study in a population aged 85 or over. NEUROSCIENCE LETTERS , 292 (3) pp. 195-198. 10.1016/S0304-3940(00)01467-1.

N

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

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; Bhatia, KP; Lees, AJ; (2000) Botulinum toxin A as treatment for drooling saliva in PD [7] (multiple letters). Neurology , 55 (4) pp. 606-607.

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.

P

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; 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) p. 469.

Q

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.

R

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.

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

S

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.

T

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

Trabzuni, D; Famulski, KS; Ahmad, M; (2000) Functional analysis of tumour necrosis factor-alpha-related apoptosis-inducing ligand (TRAIL): cysteine-230 plays a critical role in the homotrimerization and biological activity of this novel tumoricidal cytokine. BIOCHEMICAL JOURNAL , 350 pp. 505-510. 10.1042/0264-6021:3500505.

W

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.

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.

This list was generated on Sun Apr 15 02:06:36 2018 BST.