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Number of items: 85.

A

Acland, KM; Churchyard, A; Fletcher, CL; Turner, K; Lees, AJ; Dowd, PM; (1998) Panniculitis in association with apomorphine infusion. 480 - 482.

Alarcon, F; Cevallos, N; Lees, AJ; (1998) Does combined levodopa and bromocriptine therapy in Parkinson's disease prevent late motor complications? EUR J NEUROL , 5 (3) 255 - 263.

An, SF; Giometto, B; Groves, M; Scaravilli, F; (1998) Detection and localisation of HIV-1 in fixed adult AIDS brain tissue by in situ amplification. J NEUROPATH EXP NEUR , 57 (5) 490 - 490.

B

Bajaj, NPS; Shaw, C; Warner, T; RayChaudhuri, K; (1998) The genetics of Parkinson's disease and parkinsonian syndromes. JOURNAL OF NEUROLOGY , 245 (10) 625 - 633. 10.1007/s004150050258.

Bandmann, O; Marsden, CD; Wood, NW; (1998) Atypical presentations of dopa-responsive dystonia. Adv Neurol , 78 283 - 290.

Bandmann, O; Marsden, CD; Wood, NW; (1998) Genetic aspects of Parkinson's disease. MOVEMENT DISORD , 13 (2) 203 - 211.

Bandmann, O; Valente, EM; Holmans, P; Surtees, RAH; Walters, JH; Wevers, RA; ... Wood, NW; + view all (1998) Dopa-responsive dystonia: A clinical and molecular genetic study. ANN NEUROL , 44 (4) 649 - 656.

Bandmann, O; Wood, NW; (1998) Acetylator genotype and Parkinson's disease - Reply. LANCET , 351 (9096) 142 - 142.

Ben-Shlomo, Y; Churchyard, A; Head, J; Hurwitz, B; Overstall, P; Ockelford, J; Lees, AJ; (1998) Investigation by Parkinson's disease Research Group of United Kingdom into excess mortality seen with combined levodopa and selegiline treatment in patients with early mild Parkinson's disease: further results of randomised trial and confidential inquiry. BRIT MED J , 316 (7139) 1191 - 1196.

Bolton, D; Gibb, W; Lees, A; Raven, P; Gray, JA; Chen, E; Shafran, R; (1998) Neurological soft signs in obsessive compulsive disorder: standardised assessment and comparison with schizophrenia. BEHAV NEUROL , 11 (4) 197 - 204.

Brooks, DJ; Abbott, RJ; Lees, AJ; Martignoni, E; Philcox, DV; Rascol, O; ... Sagar, HJ; + view all (1998) A placebo-controlled evaluation of ropinirole, a novel D-2 agonist, as sole dopaminergic therapy in Parkinson's disease. CLINICAL NEUROPHARMACOLOGY , 21 (2) 101 - 107.

C

Cavanagh, JB; Holton, JL; Nolan, CC; Ray, DE; Naik, JT; Mantle, PG; (1998) The effects of the tremorgenic mycotoxin penitrem A on the rat cerebellum. Vet Pathol , 35 (1) 53 - 63.

Churchyard, A; Lees, A; (1998) The relation between dementia and direct involvement of the hippocampus and amygdala in PD - Reply. NEUROLOGY , 51 (5) 1517 - 1518.

Churchyard, A; Lees, A; Mathias, CJ; (1998) Autonomic effects of selegiline: possible cardiovascular toxicity in Parkinson's disease - Reply. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 65 (2) 281 - 282.

Colosimo, C; Merello, M; Hughes, AJ; Sieradzan, K; Lees, AJ; (1998) Apomorphine responses in Parkinson's disease and the pathogenesis of motor complications. NEUROLOGY , 50 (2) 573 - 574.

Colzi, A; Turner, K; Lees, AJ; (1998) Continuous subcutaneous waking day apomorphine in the long term treatment of levodopa induced interdose dyskinesias in Parkinson's disease. J NEUROL NEUROSUR PS , 64 (5) 573 - 576.

Crook, R; Verkkoniemi, A; Perez-Tur, J; Mehta, N; Baker, M; Houlden, H; ... Haltia, M; + view all (1998) A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1. NAT MED , 4 (4) 452 - 455.

Cruts, M; van Duijn, CM; Backhovens, H; Van den Broeck, M; Wehnert, A; Serneels, S; ... Van Broeckhoven, C; + view all (1998) Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population based study of presenile Alzheimer disease. HUMAN MOLECULAR GENETICS , 7 (1) 43 - 51. 10.1093/hmg/7.1.43.

D

De Strooper, B; Saftig, P; Craessaerts, K; Vanderstichele, H; Guhde, G; Annaert, W; ... Van Leuven, F; + view all (1998) Deficiency of presenilin-1 inhibits the normal cleavage of amyloid precursor protein. Nature , 391 (6665) 387 - 390. 10.1038/34910.

E

Eve, DJ; Nisbet, AP; Kingsbury, AE; Kingsbury, AE; Hewson, EL; Daniel, SE; ... Foster, OJF; + view all (1998) Basal ganglia neuronal nitric oxide synthase mRNA expression in Parkinson's disease. MOLECULAR BRAIN RESEARCH , 63 (1) 62 - 71. 10.1016/S0169-328X(98)00259-9.

F

Farrer, M; Wavrant-De Vrieze, F; Crook, R; Boles, L; Perez-Tur, J; Hardy, J; ... Lynch, T; + view all (1998) Low frequency of alpha-synuclein mutations in familial Parkinson's disease. ANNALS OF NEUROLOGY , 43 (3) 394 - 397. 10.1002/ana.410430320.

G

Giunti, P; Sabbadini, G; Sweeney, MG; Davis, MB; Veneziano, L; Mantuano, E; ... Wood, NW; + view all (1998) The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families - Frequency, clinical and genetic correlates. BRAIN , 121 459 - 467.

Glynn, P; Holton, JL; Nolan, CC; Read, DJ; Brown, L; Hubbard, A; Cavanagh, JB; (1998) Neuropathy target esterase: immunolocalization to neuronal cell bodies and axons. Neuroscience , 83 (1) 295 - 302.

Grunberg, J; Walter, J; Eckman, C; Capell, A; Schindzielorz, A; Younkin, S; ... Haass, C; + view all (1998) Truncated presenilin 2 derived from differentially spliced mRNAs does not affect the ratio of amyloid beta-peptide 1-42/1-40. NEUROREPORT , 9 (14) 3293 - 3299.

H

Hanna, MG; Davis, MB; Sweeney, MG; Noursadeghi, M; Ellis, CJ; Elliot, P; ... Marsden, CD; + view all (1998) Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion. MOVEMENT DISORD , 13 (2) 339 - 340.

Hanna, MG; Nelson, IP; Morgan-Hughes, JA; Wood, NW; (1998) MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity. J NEUROL NEUROSUR PS , 65 (4) 512 - 517.

Hanna, MG; Nelson, IP; Rahman, S; Lane, RJM; Land, J; Heales, S; ... Wood, NW; + view all (1998) Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. AM J HUM GENET , 63 (1) 29 - 36.

Hanna, MG; Stewart, J; Schapira, AHV; Wood, NW; Morgan-Hughes, JA; Murray, NMF; (1998) Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A). J NEUROL NEUROSUR PS , 65 (2) 248 - 250.

Hanna, MG; Wood, N; Kullmann, DM; (1998) Ion channels and neurological disease: DNA based diagnosis is now possible, and ion channels may be important in common paroxysmal disorders. J NEUROL NEUROSUR PS , 65 (4) 427 - 431.

Hardy, J; Duff, K; Hardy, KG; Perez-Tur, J; Hutton, M; (1998) Genetic dissection of Alzheimer's disease and related dementias: Amyloid and its relationship to tau. NATURE NEUROSCIENCE , 1 (5) 355 - 358. 10.1038/1565.

Hardy, J; Gwinn-Hardy, K; (1998) Genetic classification of primary neurodegenerative disease. SCIENCE , 282 (5391) 1075 - 1079. 10.1126/science.282.5391.1075.

Hardy, J; Perez-Tur, J; Baker, M; Farrer, M; Crook, R; Hutton, M; ... Maraganore, D; + view all (1998) Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism. AMERICAN JOURNAL OF MEDICAL GENETICS , 81 (2) 166 - 171.

Harvey, RJ; Ellison, D; Hardy, J; Hutton, M; Rogues, PK; Collinge, J; ... Rossor, MN; + view all (1998) Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine -> serine (L250S) substitution at codon 250 of the presenilin 1 gene. J NEUROL NEUROSUR PS , 64 (1) 44 - 49.

Head, J; Ben-Shlomo, Y; Lees, A; Parkinson's Dis Res Grp UK,; (1998) Reply to Jack E. Riggs' "Deprenyl, excess mortality, and epidemiological traps". CLIN NEUROPHARMACOL , 21 (4) 265 - 266.

Holcomb, L; Gordon, MN; McGowan, E; Yu, X; Benkovic, S; Jantzen, P; ... Duff, K; + view all (1998) Accelerated Alzheimer-type phenotype in transgenic mice carrying both mutant amyloid precursor protein and presenilin 1 transgenes. NATURE MEDICINE , 4 (1) 97 - 100. 10.1038/nm0198-097.

Houlden, H; Crook, R; Backhovens, H; Prihar, G; Baker, M; Hutton, M; ... Hardy, J; + view all (1998) ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease families. AM J MED GENET , 81 (1) 117 - 121.

Houser, MK; Sheean, GL; Lees, AJ; (1998) Further studies using higher doses of botulinum toxin type F for torticollis resistant to botulinum toxin type A. J NEUROL NEUROSUR PS , 64 (5) 577 - 580.

Hutton, M; Lendon, CL; Rizzu, P; Baker, M; Froelich, S; Houlden, H; ... Heutink, P; + view all (1998) Association of missense and 5 '-splice-site mutations in tau with the inherited dementia FTDP-17. NATURE , 393 (6686) 702 - 705.

J

Jarman, PR; Warner, TT; (1998) The dystonias. J Med Genet , 35 (4) 314 - 318.

K

Kapoor, R; Miller, DH; Jones, SJ; Plant, GT; Brusa, A; Gass, A; ... McDonald, WI; + view all (1998) Effects of intravenous methylprednisolone on outcome in MRI-based prognostic subgroups in acute optic neuritis. NEUROLOGY , 50 (1) 230 - 237.

L

Lambert, JC; Berr, C; Pasquier, F; Delacourte, A; Frigard, B; Cottel, D; ... Chartier-Harlin, MC; + view all (1998) Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's disease. HUMAN MOLECULAR GENETICS , 7 (9) 1511 - 1516. 10.1093/hmg/7.9.1511.

Lamont, PJ; Surtees, R; Woodward, CE; Leonard, JV; Wood, NW; Harding, AE; (1998) Clinical and laboratory findings in referrals for mitochondrial DNA analysis. ARCH DIS CHILD , 79 (1) 22 - 27.

Lees, A; (1998) In memoriam - Macdonald Critchley 2nd January 1900 15th October 1997 Bristol Nether Stowey. ARQUIVOS DE NEURO-PSIQUIATRIA , 56 (4) 865 - 867. Gold open access

Lees, AJ; (1998) Akathisia and restless legs. PSYCHOLOGICAL MEDICINE , 28 (2) 492 - 492.

Lees, AJ; Lang, AE; (1998) Movement disorders. (Vol.13).

Lees, AJ; Martinez-Martin, P; (1998) Quality of life in Parkinson's disease at the Pan-European symposium in Marbella, May 24, 1997. JOURNAL OF NEUROLOGY , 245 S1 - S1. 10.1007/PL00007729.

Leff, AP; McNabb, AW; Hanna, MG; Clarke, CRA; Larner, AJ; (1998) Complex partial status epilepticus in late-onset MELAS. EPILEPSIA , 39 (4) 438 - 441.

Lo, YM; An, SF; (1998) Generation of labeled probes by PCR. Methods Mol Med , 16 93 - 100. 10.1385/0-89603-499-2:93.

Lopes, J; Ravise, N; Vandenberghe, A; Palau, F; Ionasescu, V; Mayer, M; ... LeGuern, E; + view all (1998) Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination. HUM MOL GENET , 7 (1) 141 - 148.

Lucking, CB; Abbas, N; Durr, A; Bonifati, V; Bonnet, AM; de Broucker, T; ... French Parkinsons Dis Genetics Study Grp,; + view all (1998) Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. LANCET , 352 (9137) 1355 - 1356.

M

Marques, W; Thomas, PK; Sweeney, MG; Carr, L; Wood, NW; (1998) Dejerine-Sottas neuropathy and PMP22 point mutations: A new base pair substitution and a possible "hot spot" on Ser72. ANN NEUROL , 43 (5) 680 - 683.

Mehta, ND; Refolo, LM; Eckman, C; Sanders, S; Yager, D; Perez-Tur, J; ... Hutton, M; + view all (1998) Increased A beta 42(43) from cell lines expressing presenilin 1 mutations. ANNALS OF NEUROLOGY , 43 (2) 256 - 258. 10.1002/ana.410430217.

Moechars, D; Lorent, K; Dewachter, I; Baekelandt, V; De Strooper, B; Van Leuven, F; (1998) Transgenic mice expressing an alpha-secretion mutant of the amyloid precursor protein in the brain develop a progressive CNS disorder. Behav Brain Res , 95 (1) 55 - 64.

Morris, HR; Moriabadi, NF; Lees, AJ; Dick, DJ; Moriabadi, NF; Turjanski, D; (1998) Parkinsonism following electrical injury to the hand. MOVEMENT DISORD , 13 (3) 600 - 602.

Morris, HR; Moriabadi, NF; Lees, AJ; Dick, DJ; Turjanski, N; (1998) Parkinsonism following electrical injury to the hand (vol 13, pg 600, 1998). MOVEMENT DISORDERS , 13 (5) 864 - 864.

P

Piccini, PP; Lees, AJ; de Yebenes, JG; Pramstaller, PP; Turjanski, N; Brooks, DJ; (1998) F-18-Dopa and (18)FDG studies in 3 kindreds with familial progressive supranuclear palsy. NEUROLOGY , 50 (4) A429 - A429.

R

Rascol, O; Sieradzan, K; Peyro-Saint-Paul, H; Thalamas, C; Brefel-Courbon, C; Senard, JM; ... Lees, A; + view all (1998) Efaroxan, an alpha-2 antagonist, in the treatment of progressive supranuclear palsy. MOVEMENT DISORD , 13 (4) 673 - 676.

Ray, DE; Holton, JL; Nolan, CC; Cavanagh, JB; Harpur, ES; (1998) Neurotoxic potential of gadodiamide after injection into the lateral cerebral ventricle of rats. AJNR Am J Neuroradiol , 19 (8) 1455 - 1462.

S

Saftig, P; de Strooper, B; (1998) Downregulation of PS1 expression in neurons decreases beta-amyloid production: a biochemical link between the two major familial Alzheimer's disease genes. Mol Psychiatry , 3 (4) 287 - 289.

Sagdullaev, BT; Abramov, AY; Gagelgans, AI; Dzhakhangirov, FN; Usmanov, PB; (1998) Effect of a diterpene alkaloid series on calcium homeostases of rat cardiomyocites - Structure-activity bond. KHIM PRIR SOEDIN+ (4) 523 - 526.

Samuel, M; Caputo, E; Brooks, DJ; Schrag, A; Scaravilli, T; Branston, NM; ... Quinn, NP; + view all (1998) A study of medial pallidotomy for Parkinson's disease: clinical outcome, MRI location and complications. BRAIN , 121 59 - 75.

Scaravilli, F; Lindsay, R; Groves, M; An, SF; Giometto, B; (1998) Axotomy-induced apoptosis in adult rat primary sensory neurons and effect of administration of neurotrophins. J NEUROPATH EXP NEUR , 57 (5) 491 - 491.

Schrag, A; Kingsley, D; Phatouros, C; Mathias, CJ; Lees, AJ; Daniel, SE; Quinn, NP; (1998) Clinical usefulness of magnetic resonance imaging in multiple system atrophy. J NEUROL NEUROSUR PS , 65 (1) 65 - 71.

Seery, JP; Bryant, DJ; Jenkinson, G; Schwieso, JE; Houlden, HJ; Changani, KK; ... Taylor-Robinson, SD; + view all (1998) Intravenous intralipid infusion in hepatic steatosis: an in vivo hepatic phosphorus-31 magnetic resonance spectroscopy study. HEPATOL RES , 12 (1) 50 - 58.

Simons, M; Keller, P; De Strooper, B; Beyreuther, K; Dotti, CG; Simons, K; (1998) Cholesterol depletion inhibits the generation of beta-amyloid in hippocampal neurons. Proc Natl Acad Sci U S A , 95 (11) 6460 - 6464.

Spencer, JP; Jenner, P; Daniel, SE; Lees, AJ; Marsden, DC; Halliwell, B; (1998) Conjugates of catecholamines with cysteine and GSH in Parkinson's disease: possible mechanisms of formation involving reactive oxygen species. J Neurochem , 71 (5) 2112 - 22.

Stanyer, L; Cooper, MB; Betteridge, DJ; Smith, CCT; (1998) Stimulatory actions of native and oxidised plasma lipoproteins on beta-amyloid fibrillogenesis in vitro. ATHEROSCLEROSIS , 141 (1) 183 - 183.

Stevanin, G; David, G; Abbas, N; Durr, A; Holmberg, M; Duyckaerts, C; ... Brice, A; + view all (1998) Spinocerebellar ataxia 7. In: Rubinsztein, DC and Hayden, MR, (eds.) Analysis of triplet repeat disorders. Bios Scientific: Oxford.

Stevanin, G; Giunti, P; David, G; Belal, S; Durr, A; Ruberg, M; ... Brice, A; + view all (1998) De novo expansion of intermediate alleles in spinocerebellar ataxia 7. HUM MOL GENET , 7 (11) 1809 - 1813.

T

Turjanski, N; Lees, AJ; Brooks, DJ; (1998) Dopaminergic dysfunction in patients with restless legs: [F-18]dopa and [C-11]raclopride PET studies. NEUROLOGY , 50 (4) A391 - A391.

V

Valente, EM; Warner, TT; Jarman, PR; Mathen, D; Fletcher, NA; Marsden, CD; ... Wood, NW; + view all (1998) The role of DYT1 in primary torsion dystonia in Europe. BRAIN , 121 2335 - 2339.

Vaughan, J; Durr, A; Tassin, J; Bereznai, B; Gasser, T; Bonifati, V; ... Wood, NW; + view all (1998) The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease. Ann Neurol , 44 (2) 270 - 273. 10.1002/ana.410440221.

Vaughan, J; Durr, A; Tassin, J; Bereznai, B; Gasser, T; Bonifati, V; ... Eurpean Consortium Genetic Susceptibility Parki,; + view all (1998) The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases. ANN NEUROL , 44 (2) 270 - 273.

Vaughan, JR; Farrer, MJ; Wszolek, ZK; Gasser, T; Durr, A; Agid, Y; ... Wood, NW; + view all (1998) Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. HUM MOL GENET , 7 (4) 751 - 753.

Vaughan, JR; Farrer, MJ; Wszolek, ZK; Gasser, T; Durr, A; Agid, Y; ... Wood, NW; + view all (1998) Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD). Hum Mol Genet , 7 (4) 751 - 753.

W

Wang, HC; Brown, P; Lees, AJ; (1998) Acute movement disorders with bilateral basal ganglia lesions in uremia. MOVEMENT DISORD , 13 (6) 952 - 957.

Warner, TT; Jarman, P; (1998) The molecular genetics of the dystonias. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 64 (4) 427 - 429. 10.1136/jnnp.64.4.427.

Warner, TT; Schapira, AHV; (1998) The role of the alpha-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom. J NEUROL NEUROSUR PS , 65 (3) 378 - 379.

Warr, TJ; Ward, SJ; Darling, JL; Thomas, DGT; (1998) Identification of chromosomal gains and losses in paediatric malignant astrocytoma by comparative genomic hybridisation. British Journal of Cancer , 78 157 - ?.

Wood, NW; (1998) Diagnosing Friedreich's ataxia. ARCH DIS CHILD , 78 (3) 204 - 207.

Wood, NW; (1998) Genetic risk factors in Parkinson's disease. ANNALS OF NEUROLOGY , 44 (3) S58 - S62.

Wood, NW; (1998) Genetic risk factors in Parkinson's disease. In: Olanow, CW and Jenner, P, (eds.) Beyond the decade of the brain: neuroprotection in Parkinson's disease. (115 - 120). Wells Medical: Tunbridge Wells.

Wu, WS; Holmans, P; Wavrant-Devrieze, F; Shears, S; Kehoe, P; Crook, R; ... Goate, A; + view all (1998) Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION , 280 (7) 619 - 622. 10.1001/jama.280.7.619.

Z

Zhang, Z; Hartmann, H; Do, VM; Abramowski, D; Sturchler-Pierrat, C; Staufenbiel, M; ... Yankner, BA; + view all (1998) Destabilization of beta-catenin by mutations in presenilin-1 potentiates neuronal apoptosis. Nature , 395 (6703) 698 - 702. 10.1038/27208.

Zori, RT; Gardner, JL; Zhang, J; Mullan, MJ; Shah, R; Osborn, AR; ... Yang, TP; + view all (1998) Newly described form of X-linked arthrogryposis maps to the long arm of the human X chromosome. AM J MED GENET , 78 (5) 450 - 454.

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