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Number of items: 63.

A

Abramov, AY; Zamaraeva, MV; Hagelgans, AI; Azimov, RR; Krasilnikov, OV; (2001) Influence of plant terpenoids on the permeability of mitochondria and lipid bilayers. BBA-BIOMEMBRANES , 1512 (1) 98 - 110.

B

Bajaj, NPS; Lees, A; Giovannoni, G; Bhatia, K; Quinn, N; (2001) Movement disorder in Whipple's disease. NEUROLOGY , 56 (8) A119-A119.

Bandopadhyay, R; de Silva, R; Khan, N; Graham, E; Vaughan, J; Engelender, S; Ross, C; ... Lees, A; + view all (2001) No pathogenic mutations in the synphilin-1 gene in Parkinson's disease. NEUROSCI LETT , 307 (2) 125 - 127.

Ben Shlomo, Y; Head, J; Lees, A; (2001) Selegiline and mortality in subjects with Parkinson's disease: a longitudinal community study. Neurology , 57 (2) p. 369.

C

Caselli, RJ; Osborne, D; Reiman, EM; Hentz, JG; Barbieri, CJ; Saunders, AM; Hardy, J; ... Alexander, GE; + view all (2001) Preclinical cognitive decline in late middle-aged asymptomatic apolipoprotein E-e4/4 homozygotes: a replication study. JOURNAL OF THE NEUROLOGICAL SCIENCES , 189 (1-2) pp. 93-98. 10.1016/S0022-510X(01)00577-9.

Cordivari, C; Misra, VP; Catania, S; Lees, AJ; (2001) Treatment of dystonic clenched fist with botulinum toxin. MOVEMENT DISORD , 16 (5) 907 - 913.

D

Davenport, WJ; Siegel, AM; Dichgans, J; Drigo, P; Mammi, I; Pereda, P; Wood, NW; (2001) CCM1 gene mutations in families segregating cerebral cavernous malformations. NEUROLOGY , 56 (4) 540 - 543.

Davies, NP; Hanna, MG; (2001) Inherited muscle and brain channelopathies. Expert Rev Neurother , 1 (2) pp. 247-265. 10.1586/14737175.1.2.247.

Davies, NP; Hanna, MG; (2001) The genetic neurological channelopathies. In: Scolding, N, (ed.) Contemporary treatments in neurology. (pp. 398-440). Butterworth-Heinemann: Oxford.

Doder, M; Rabiner, EI; Turjanski, N; Lees, AJ; Brooks, DJ; (2001) Functional imaging of tremor in Parkinson's disease with [C-11]-WAY 100635 PET. NEUROLOGY , 56 (8) A271-A272.

de Silva, R; Weiler, M; Morris, HR; Martin, ER; Wood, NW; Lees, AJ; (2001) Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy. NEUROSCI LETT , 311 (3) 145 - 148.

E

Elinder, F; Mannikko, R; Larsson, HP; (2001) S4 charges move close to residues in the pore domain during activation in a K channel. JOURNAL OF GENERAL PHYSIOLOGY , 118 (1) pp. 1-10. 10.1085/jgp.118.1.1.

F

Farrer, M; Destee, A; Levecque, C; Singleton, A; Engelender, S; Becquet, E; Mouroux, V; ... Chartier-Harlin, MC; + view all (2001) Genetic analysis of synphilin-1 in familial Parkinson's disease. NEUROBIOLOGY OF DISEASE , 8 (2) pp. 317-323. 10.1006/nbdi.2000.0326.

Feliciani, M; Warner, T; (2001) Cervical dystonia. In: The Year in Neurology 2001. (pp. 1-50). Oxford Clinical Publishing Services

G

Gambling, L; Danzeisen, R; Gair, S; Lea, RG; Charania, Z; Solanky, N; Joory, KD; ... McArdle, HJ; + view all (2001) Effect of iron deficiency on placental transfer of iron and expression of iron transport <i>in vivo</i> and <i>in vitro</i>. Biochemical Journal , 356 pp. 883-889.

Gibson, GE; Kingsbery, AE; Xu, H; Lindsay, JG; Daniel, S; Foster, O; Lees, AJ; (2001) Deficit in a Krebs cycle mitochondrial enzyme in brains from patients with Parkinson's disease. JOURNAL OF NEUROCHEMISTRY , 78 p. 132.

Guerin, CJ; Nolan, CC; Mavroudis, G; Lister, T; Davidson, GM; Holton, JL; Ray, DE; (2001) The dynamics of blood-brain barrier breakdown in an experimental model of glial cell degeneration. NEUROSCIENCE , 103 (4) pp. 873-883. 10.1016/S0306-4522(01)00015-X.

H

Hall, C.; Brown, M.; Jacobs, T.; Ferrari, G.; Cann, N.; Teo, M.; Monfries, C.; (2001) Collapsin response mediator protein switches RhoA and Rac1 morphology in N1E-115 neuroblastoma cells and is regulated by Rho kinase. Journal of Biological Chemistry , 276 (46) pp. 43482-43486. 10.1074/jbc.C100455200. Gold open access

Hall, C.; Michael, G.J.; Cann, N.; Ferrari, G.; Teo, M.; Jacobs, T.; Monfries, C.; (2001) alpha 2-chimaerin, a Cdc42/Rac1 regulator, is selectively expressed in the rat embryonic nervous system and is involved in neuritogenesis in N1E-115 neuroblastoma cells. The Journal of Neuroscience , 21 (14) pp. 5191-5202. Green open access
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Hardy, J; (2001) Genetic dissection of neurodegenerative disease. CLINICAL NEUROSCIENCE RESEARCH , 1 (1-2) pp. 134-141. 10.1016/S1566-2772(00)00013-X.

Holton, J.L.; Ghiso, J.; Lashle, T.; Rostagno, A.; Guerin, C.J.; Gibb, G.; Houlden, H.; ... Revesz, T.; + view all (2001) Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia. American Journal of Pathology , 158 (2) pp. 515-526. Green open access
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Houlden, H; Parlette, E; Domínguez, K; Hoffler, KD; Chui, CK; (2001) Development of multi-dimensional wavelet methods for simulation aerodynamic modeling. 39th Aerospace Sciences Meeting and Exhibit

Houlden, H.; King, R.H.M.; Hashemi-Nejad, A.; Wood, N.W.; Mathias, C.J.; Reilly, M.; Thomas, P.K.; (2001) A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V. Annals of Neurology , 49 (4) pp. 521-525. 10.1002/ana.103.

Houlden, H.; King, R.H.M.; Wood, N.W.; Thomas, P.K.; Reilly, M.M.; (2001) Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin. Brain , 124 (5) pp. 907-915. 10.1093/brain/124.5.907.

J

Jouvenceau, A.; Eunson, L.H.; Spauschus, A.; Ramesh, V.; Zuberi, S.M.; Kullmann, D.M.; Hanna , M.G.; (2001) Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel. The Lancet , 358 (9284) pp. 801-807. 10.1016/S0140-6736(01)05971-2.

K

Khan, NL; Pavese, N; Wood, NW; Lees, AJ; Brooks, DJ; Piccini, P; (2001) An 18F dopa PET study of disease progression and subclinical nigrostriatal dysfunction in a Parkin kindred. NEUROLOGY , 56 (8) A249-A249.

L

Lang, AE; Lees, AJ; (2001) Editorial. Movement Disorders , 16 (1) pp. 1-2. 10.1002/1531-8257(200101)16:1&lt;1::AID-MDS1015&gt;3.0.CO;2-5.

Lee, MF; Sweeney, M; Stephenson, D; Davis, M; Houlden, H; Wood, NW; Scaravilli, F; (2001) Genetic study of the mutilated foot rat, an animal model for human hereditary sensory neuropathy. ANN NEUROL , 50 (3) S51 - S51.

Lees, A; (2001) Jumpers. MOVEMENT DISORD , 16 (3) 403 - 404.

Lees, AJ; (2001) Apomorphine infusions for treatment of advanced Parkinson's disease. In: Krauss, JK and Jankovic, J and Grossman, RG, (eds.) Surgery for Parkinson's disease and movement disorders. (pp. 252-257). Lippincott, Williams & Wilkins: London.

Leonard, A.J.; Evans, I.M.; Pickard, M.R.; Bandopadhyay, R.; Sinha, A.K.; Ekins, R.P.; (2001) Thyroid hormone receptor expression in rat placenta. Placenta , 22 (4) pp. 353-359. 10.1053/plac.2000.0617.

Leonard, AJ; Evans, IM; Pickard, MR; Bandopadhyay, R; Sinha, AK; Ekins, RP; (2001) Thyroid hormone receptor expression in rat placenta. PLACENTA , 22 (4) 353 - 359.

M

McEntagart, M.; Norton, N.; Williams, H.; Teare, M.D.; Dunstan, M.; Baker, P.; Houlden, H.; ... Rahman, N.; + view all (2001) Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14. The American Journal of Human Genetics , 68 (5) pp. 1270-1276. 10.1086/320122.

Meschia, JF; Brown, RD; Brott, TG; Hardy, J; Atkinson, EJ; O'Brien, PC; (2001) Feasibility of an affected sibling pair study in ischemic stroke - Results of a 2-center family history registry. STROKE , 32 (12) pp. 2939-2941. 10.1161/hs1201.099795.

Misbahuddin, A; Warner, TT; (2001) Dystonia: an update on genetics and treatment. CURR OPIN NEUROL , 14 (4) 471 - 475.

Morris, HR; Khan, MN; Janssen, JC; Brown, JM; Perez-Tur, J; Baker, M; Ozansoy, M; ... Rossor, MN; + view all (2001) The genetic and pathological classification of familial frontotemporal dementia. ARCH NEUROL-CHICAGO , 58 (11) 1813 - 1816.

Munchau, A; Bahlke, G; Allen, PJ; Quinn, NP; Lees, AJ; Rothwell, JC; Palmer, JD; (2001) Polymyography combined with time-locked video recording (video EMG) for presurgical assessment of patients with cervical dystonia. EUR NEUROL , 45 (4) 222 - 228.

N

Nardocci, N; Fernandez-Alvarez, E; Wood, NW; Spacey, SD; Richter, A; (2001) The paroxysmal dyskinesias. In: Guerrini, R and Aicardi, J and Andermann, F and Hallett, M, (eds.) Epilepsy and movement disorders. (pp. 125-139). Cambridge University Press: Cambridge.

Nath, U; Ben-Shlomo, Y; Thomson, RG; Morris, HR; Wood, NW; Lees, AJ; Burn, DJ; (2001) Clinical features of Progressive Supranuclear Palsy (PSP) in the United Kingdom. NEUROLOGY , 56 (8) A458-A458.

Nath, U; Morris, H; Thomson, R; Ben-Shlomo, Y; Wood, N; Lees, A; Burn, DJ; (2001) The prevalence of progressive supranuclear palsy in the United Kingdom. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 70 (2) pp. 271-272.

O

O'Farrell, C; Murphy, DD; Petrucelli, L; Singleton, AB; Hussey, J; Farrer, M; Hardy, J; ... Cookson, MR; + view all (2001) Transfected synphilin-1 forms cytoplasmic inclusions in HEK293 cells. MOLECULAR BRAIN RESEARCH , 97 (1) pp. 94-102. 10.1016/S0169-328X(01)00292-3.

P

Page, RA; Davie, CA; MacManus, D; Dooley, J; Walshe, J; Miller, DH; Lees, AJ; (2001) Magnetic resonance spectroscopy of patients with Wilson's disease. J NEUROL NEUROSUR PS , 70 (2) 274 - 275.

Patel, H; Hart, PE; Warner, T; Allen, I; Phillimore, HE; Silver, JR; Wood, NW; ... Crosby, AH; + view all (2001) Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci. AM J MED GENET , 102 (1) 68 - 72.

Patel, H; Hart, PE; Warner, TT; Houlston, RS; Patton, MA; Jeffery, S; Crosby, AH; (2001) The Silver syndrome variant of hereditary spastic paraplegia maps to 11q12-q14 with evidence for genetic heterogeneity within this subtype. AMERICAN JOURNAL OF HUMAN GENETICS , 69 (4) p. 512.

Piccini, P; de Yebenez, J; Lees, AJ; Ceravolo, R; Turjanski, N; Pramstaller, P; Brooks, DJ; (2001) Familial progressive supranuclear palsy - Detection of subclinical cases using F-18-dopa and (18)fluorodeoxyglucose positron emission tomography. ARCHIVES OF NEUROLOGY , 58 (11) pp. 1846-1851. 10.1001/archneur.58.11.1846.

Placzek, MR; Misbahuddin, A; Chaudhuri, KR; Wood, NW; Bhatia, KP; Warner, TT; (2001) Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor gene. J NEUROL NEUROSUR PS , 71 (2) 262 - 264.

Plun-Favreau, H; Elson, G; Chabbert, M; Froger, J; deLapeyriere, O; Lelievre, E; Guillet, C; ... Chevalier, S; + view all (2001) The ciliary neurotrophic factor receptor alpha component induces the secretion of and is required for functional responses to cardiotrophin-like cytokine. EMBO J , 20 (7) 1692 - 1703.

R

Rees, J.H.; Hain, S.F.; Johnson, M.R.; Hughes, R.A.C.; Costa, D.C.; Ell, P.J.; Keir, G.; (2001) The role of [18F]fluoro-2-deoxyglucose-PET scanning in the diagnosis of paraneoplastic neurological disorders. Brain , 124 (11) pp. 2223-2231. 10.1093/brain/124.11.2223.

Reilly, MM; Lee, MJ; Sweeney, MG; Stephenson, D; Davis, M; Groves, M; Houlden, H; ... Scaravilli, F; + view all (2001) Genetic analysis of the mutilated foot (mf) rat: an animal model for human hereditary sensory neuropathy. AM J HUM GENET , 69 (4) 501 - 501.

Rosenberg, RN; Aminoff, M; Boller, F; Soerensen, PS; Griggs, RC; Hallett, M; Johnson, RT; ... Zochodne, D; + view all (2001) Reporting clinical trials: full access to all the data. Neurorehabil Neural Repair , 15 (3) pp. 157-158.

Ryten, M; Hoebertz, A; Burnstock, G; (2001) Sequential expression of three receptor subtypes for extracellular ATP in developing rat skeletal muscle. Developmental Dynamics , 221 (3) pp. 331-341. 10.1002/dvdy.1147.

S

Smith, CCT; Hyatt, PJ; Stanyer, L; Betteridge, DJ; (2001) Platelet secretion of beta-amyloid is increased in hypercholesterolaemia. BRAIN RES , 896 (1-2) 161 - 164.

Stewart, VC; Heslegrave, AJ; Brown, GC; Clark, JB; Heales, SJR; (2001) Glutamate receptor activation mediates nitric oxide dependent damage to neuronal mitochondria. J NEUROCHEM , 78 84 - 84.

Sukocheva, OA; Abramov, AY; Levitskaya, JO; Gagelgans, AI; Carpenter, DO; (2001) Modulation of intracellular Ca2+ concentration by vitamin B-12 in rat thymocytes. BLOOD CELL MOL DIS , 27 (5) 812 - 824. 10.1006/bcmd.2001.0450.

V

Valente, EM; Brancati, F; Ferraris, A; Bentivoglio, AR; Bonifati, V; Vaughan, J; Pizzuti, A; ... European Consortium Genet Suscepti, ; + view all (2001) PARK6 is a major locus in early-onset parkinsonism. AM J HUM GENET , 69 (4) 500 - 500.

Vaughan, JR; Davis, MB; Wood, NW; (2001) Genetics of Parkinsonism: a review. ANN HUM GENET , 65 111 - 126.

Visvikis, D; Gacinovic, S; Erlandsson, K; O'Sullivan, JD; Lees, AJ; Katzenschlager, R; Costa, DC; (2001) Parametric mapping of I-123-FPCIT (DaTSCAN) binding in normal volunteers and Parkinson's disease. In: EUR J NUCL MED. (pp. 1009 - 1009). SPRINGER-VERLAG

W

Warr, T; Ward, S; Burrows, L; Harding, B; Wilkins, P; Harkness, W; Hayward, R; ... Thomas, D; + view all (2001) Identification of extensive genomic loss and gain by comparative genomic hybridisation in malignant astrocytoma in children and young adults. GENES CHROMOSOMES & CANCER , 31 (1) pp. 15-22. 10.1002/gcc.1113.

Wilkinson, PA; Bradley, JL; Warner, TT; (2001) Friedreich's ataxia presenting as an isolated spastic paraparesis. J NEUROL NEUROSUR PS , 71 (5) 709 - 709.

Willis, T; Roper, HP; Houlden, H; (2001) Clinical experience of giant axonal neuropathy in two families, each associated with novel mutations in the gigaxonin gene. NEUROMUSCULAR DISORD , 11 (6-7) 662 - 662.

Wood, NW; Kinton, L; Hanna, MG; (2001) Genetics of the overlap between epilepsy and movement disorders. In: Guerrini, R and Aicardi, J and Andermann, F and Hallett, M, (eds.) Epilepsy and movement disorders. (pp. 451-464). Cambridge University Press: Cambridge.

Wood, NW; Lee, MJ; (2001) The spinocerebellar ataxias-genotype-phenotype correlation. Acta Neurologica Taiwanica , 10 (1) pp. 9-13.

Worth, PF; Wood, NW; (2001) Genotype to phenotype in the spinocerebellar ataxias. In: Malcom, S and Goodship, J, (eds.) Genotype to phenotype. (pp. 165-187). Bios Scientific Publishers

This list was generated on Sun Apr 15 02:06:09 2018 BST.