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Number of items: 162.

A

Abramov, A.Y. and Jacobson, J. and Wientjes, F. and Hothersall, J. and Canevari, L. and Duchen, M.R. (2005) Expression and modulation of an NADPH oxidase in mammalian astrocytes. Journal of Neuroscience , 25 (40) pp. 9176-9184. 10.1523/JNEUROSCI.1632-05.2005.
An open access version is available from UCL Discovery
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Abramov, AY and Canevari, L and Duchen, MR (2005) Expression, function and modulation of an NADPH oxidase in mammalian astrocytes. In: BIOPHYSICAL JOURNAL. (pp. 256A - 257A). BIOPHYSICAL SOCIETY

Abramov, AY and Duchen, MR (2005) Mechanisms underlying the loss of mitochondrial potential calcium homeostasis in neurons during glutamate excitotoxicity. In: JOURNAL OF NEUROCHEMISTRY. (pp. 246 - 246).

Abramov, AY and Duchen, MR (2005) The role of an astrocytic NADPH oxidase in the neurotoxicity of amyloid beta peptides. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES , 360 (1464) 2309 - 2314. 10.1098/rstb.2005.1766.
An open access publication

Abramov, AY and Jacobson, J and Wientjes, F and Hothersall, J and Canevari, L and Duchen, MR (2005) Expression and modulation of an NADPH oxidase in mammalian astrocytes. J NEUROSCI , 25 (40) 9176 - 9184. 10.1523/JNEUROSCI.1632-05.2005.

Ahmadi, K.R. and Weale, M.E. and Xue, Z.Y. and Soranzo, N. and Yarnall, D.P. and Briley, J.D. and Maruyama, Y. and Kobayashi, M. and Wood, N.W. and Spurr, N.K. and Burns, D.K. and Roses, A.D. and Saunders, A.M. and Goldstein, D.B. (2005) A single-nucleotide polymorphism tagging set for human drug metabolism and transport. Nature Genetics , 37 (1) pp. 84-89. 10.1038/ng1488.

Ahmadi, KR and Weale, ME and Xue, ZYY and Soranzo, N and Yarnall, DP and Briley, JD and Maruyama, Y and Kobayashi, M and Wood, NW and Spurr, NK and Burns, DK and Roses, AD and Saunders, AM and Goldstein, DB (2005) A single-nucleotide polymorphism tagging set for human drug metabolism and transport. NAT GENET , 37 (1) 84 - 89. 10.1038/ng1488.

Archer, HA and Schott, JM and Barnes, J and Fox, NC and Holton, JL and Revesz, T and Cipolotti, L and Rossor, MN (2005) Knight's move thinking? Mild cognitive impairment in a chess player. NEUROCASE , 11 (1) 26 - 31. 10.1080/13554790490896875.

B

Bandopadhyay, R and Kingsbury, AE and Lees, AJ (2005) Expression pattern of synphilin-1 and parkin in control and Parkinson's disease brain. In: MOVEMENT DISORDERS. (pp. S122 - S122). WILEY-LISS

Bandopadhyay, R and Kingsbury, AE and Muqit, MM and Harvey, K and Reid, AR and Kilford, L and Engelender, S and Schlossmacher, MG and Wood, NW and Latchman, DS and Harvey, RJ and Lees, AJ (2005) Synphilin-1 and parkin show overlapping expression patterns in human brain and form aggresomes in response to proteasomal inhibition. NEUROBIOL DIS , 20 (2) 401 - 411. 10.1016/j.nbd.2005.03.021.

Bandopadhyay, R and Miller, DW and Kingsbury, AE and Jowett, TP and Kaleem, MM and Pittman, AM and de Silva, R and Cookson, MR and Lees, AJ (2005) Development, characterisation and epitope mapping of novel monoclonal antibodies for DJ-1 (PARK7) protein. NEUROSCI LETT , 383 (3) 225 - 230. 10.1016/j.neulet.2005.04.024.

Bobb, AJ and Addington, AM and Sidransky, E and Gornick, MC and Lerch, JP and Greenstein, DK and Clasen, LS and Sharp, WS and Inoff-Germain, G and Vrieze, FWD and Arcos-Burgos, M and Straub, RE and Hardy, JA and Castellanos, FX and Rapoport, JL (2005) Support for association between ADHD and two candidate genes: NET1 and DRD1. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 134B (1) 67 - 72. 10.1002/ajmg.b.30142.

Borhani-Haghighi, A and Houlden, H and Lankarani, KB and Taghavi, A and Masnadi, K (2005) A novel sequence variation in the first genetically confirmed Allgrove syndrome in Iran. In: JOURNAL OF NEUROLOGY. (pp. 59 - 59). DR DIETRICH STEINKOPFF VERLAG

Bras, JM and Guerreiro, RJ and Ribeiro, MH and Januario, C and Morgadinho, A and Oliveira, CR and Cunha, L and Hardy, J and Singleton, A (2005) G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort. MOVEMENT DISORD , 20 (12) 1653 - 1655.

C

Cavalleri, GL and Lynch, JM and Depondt, C and Burley, MW and Wood, NW and Sisodiya, SM and Goldstein, DB (2005) Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here? BRAIN , 128 1832 - 1840. 10.1093/brain/awh524.

Cavallieri, GL and Kinirons, P and Shahwan, A and McCarthy, M and Doherty, CP and Wood, NW and Sisodiya, S and Goldstein, DB and Delanty, N (2005) Genetic variation in GABAG2 - Lessons to be learned from association studies in two large epilepsy cohorts. In: EPILEPSIA. (pp. 366 - 366). BLACKWELL PUBLISHING

Clarimon, J and Asgeirsson, H and Singleton, A and Jakobsson, F and Hjaltason, H and Hardy, J and Sveinbjornsdottir, S (2005) Torsin A haplotype predisposes to idiopathic dystonia. ANNALS OF NEUROLOGY , 57 (5) 765 - 767. 10.1002/ana.20485.

Clarimon, J and Johnson, J and Dogu, O and Horta, W and Khan, N and Lees, AJ and Hardy, J and Singleton, A (2005) Defining the ends of Parkin Exon 4 deletions in two different families with Parkinson's disease. AM J MED GENET B , 133B (1) 120 - 123. 10.1002/ajmg.b.30119.

Connell, JW and Rodriguez-Martin, T and Gibb, GM and Kahn, NM and Grierson, AJ and Hanger, DP and Revesz, T and Lantos, PL and Anderton, BH and Gallo, JM (2005) Quantitative analysis of tau isoform transcripts in sporadic tauopathies. MOL BRAIN RES , 137 (1-2) 104 - 109. 10.1016/j.molbrainres.2005.02.014.

Crowther, DC and Kinghorn, KJ and Miranda, E and Page, R and Curry, JA and Duthie, FA and Gubb, DC and Lomas, DA (2005) Intraneuronal Abeta, non-amyloid aggregates and neurodegeneration in a Drosophila model of Alzheimer's disease. Neuroscience , 132 (1) 123 - 135. 10.1016/j.neuroscience.2004.12.025.

D

Davies, N.P. and Imbrici, P. and Fialho, D. and Herd, C. and Bilsland, L.G. and Weber, A. and Mueller, R. and Hilton-Jones, D. and Ealing, J. and Boothman, B.R. and Giunti, P. and Parsons, L.M. and Thomas, M. and Manzur, A.Y. and Jurkat-Rott, K. and Lehmann-Horn, F. and Chinnery, P.F. and Rose, M. and Kullmann, D.M. and Hanna, M.G. (2005) Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation. Neurology , 65 (7) pp. 1083-1089. 10.1212/01.wnl.0000178888.03767.74.

Davies, NP and Imbrici, P and Fialho, D and Herd, C and Bilsland, LG and Weber, A and Mueller, R and Hilton-Jones, D and Ealing, J and Boothman, BR and Giunti, P and Parsons, LM and Thomas, M and Manzur, AY and Jurkat-Rott, K and Lehmann-Horn, F and Chinnery, PF and Rose, M and Kullmann, DM and Hanna, MG (2005) Andersen-Tawil syndrome - New potassium channel mutations and possible phenotypic variation. NEUROLOGY , 65 (7) 1083 - 1089.

Davies, NP and Imbrici, P and Fialho, D and Herd, C and Bilsland, LG and Weber, A and Mueller, R and Hilton-Jones, D and Ealing, J and Boothman, BR and Giunti, P and Parsons, LM and Thomas, M and Manzur, AY and Jurkat-Rott, K and Lehmann-Horn, F and Chinnery, PF and Rose, M and Kullmann, DM and Hanna, MG (2005) Andersen-Tawil syndrome: New potassium channel mutations and possible phenotypic variation. Neurology , 65 (7) 1083 - 1089.

Depondt, C and Cavalleri, GL and Shorvon, SD and Wood, NW and Sisodiya, SM and Goldstein, DB (2005) Association study of five sodium channel genes in epilepsy and antiepileptic drug response. In: EPILEPSIA. (pp. 90 - 91). BLACKWELL PUBLISHING

Docherty, RJ and Charlesworth, G and Farrag, K and Bhattacharjee, A and Costa, S (2005) The use of the rat isolated vagus nerve for functional measurements of the effect of drugs in vitro. J Pharmacol Toxicol Methods , 51 (3) 235 - 242. 10.1016/j.vascn.2004.08.011.

E

Edwards-Lee, T and Ringman, JM and Chung, J and Werner, J and Morgan, A and Hyslop, PS and Thompson, P and Dutton, R and Mlikotic, A and Rogaeva, E and Hardy, J (2005) An African American family with earlyonset Alzheimer disease and an APP (T714I) mutation. NEUROLOGY , 64 (2) 377 - 379.

Eriksson, S and Trupke, M and Powell, HF and Sahagun, D and Sinclair, CDJ and Curtis, EA and Sauer, BE and Hinds, EA and Moktadir, Z and Gollasch, CO and Kraft, M (2005) Integrated optical components on atom chips. EUR PHYS J D , 35 (1) 135 - 139. 10.1140/epjd/e2005-00092-x.

Eunson, LH and Graves, TD and Hanna, MG (2005) New calcium channel mutations predict aberrant RNA splicing in episodic ataxia. NEUROLOGY , 65 (2) 308 - 310.

Eunson, LH and Graves, TD and Hanna, MG (2005) New calcium channel mutations predict aberrant RNA splicing in episodic ataxia. Neurology , 65 (2 SUPPL. 1) 308 - 310.

Everett, CM and Graves, TD and Lad, S and Jager, HR and Thom, M and Isenberg, DA and Hanna, MG (2005) CNS Lupus in the absence of systemic disease activity. In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. S271 - S271). ELSEVIER SCIENCE BV

F

Fung, HC and Evans, J and Evans, W and Duckworth, J and Pittman, A and de Silva, R and Myers, A and Hardy, J (2005) The architecture of the tau haplotype block in different ethnicities. NEUROSCI LETT , 377 (2) 81 - 84. 10.1016/j.neulet.2004.11.072.

G

Gandhi, S and Abou-Sleiman, PM and Healy, DG and Weale, M and Gilks, W and Ahmadi, K and Goldstein, DB and Wood, NW (2005) Population genetic approaches to neurological disease: Parkinson's disease as an example. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES , 360 (1460) 1573 - 1578. 10.1098/rstb.2005.1687.
An open access publication

Gandhi, S and Muqit, M and Ganguly, M and Abou-Sleiman, PM and Wood, NW and Holton, JL and Revesz, T (2005) PINK1 protein distribution in normal human brain and Parkinson's disease. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 221 - 222). BLACKWELL PUBLISHING LTD

Gandhi, S and Wood, NW (2005) Molecular pathogenesis of Parkinson's disease. Hum Mol Genet , 14 (18) 2749 - 2755. 10.1093/hmg/ddi308.

Gandhi, S and Wood, NW (2005) Molecular pathogenesis of Parkinson's disease. Hum Mol Genet , 14 Spec No. 2 2749 - 2755.

Geddes, J and McLaughlin, J and Revesz, T (2005) Robin Osler Barnard (21 October 1932-10 May 2005) - Obituary. NEUROPATH APPL NEURO , 31 (5) 561 - 562. 10.1111/j.1365-2990.2005.00695.x.

Geser, F and Seppi, K and Stampfer-Kountchev, M and Kollensperger, M and Diem, A and Ndayisaba, JP and Ostergaard, K and Dupont, E and Cardozo, A and Tolosa, E and Abele, M and Dodel, R and Klockgether, T and Ghorayeb, I and Yekhlef, F and Tison, F and Daniels, C and Kopper, F and Deuschl, G and Coelho, M and Ferreira, J and Rosa, MM and Sampaio, C and Bozi, M and Schrag, A and Hooker, J and Kim, H and Scaravilli, T and Mathias, CJ and Fowler, C and Wood, N and Quinn, N and Widner, H and Nilsson, CF and Lindvall, O and Schimke, N and Eggert, KM and Oertel, W and del Sorbo, F and Carella, F and Albanese, A and Pellecchia, MT and Barone, P and Djaldetti, R and Meco, G and Colosimo, C and Gonzalez-Mandly, A and Berciano, J and Gurevich, T and Giladi, N and Galitzky, M and Ory, F and Rascol, O and Kamm, C and Buerk, K and Maass, S and Gasser, T and Poewe, W and Wenning, GK and EMSA-SG, (2005) The European Multiple System Atrophy-Study Group (EMSA-SG). JOURNAL OF NEURAL TRANSMISSION , 112 (12) 1677 - 1686. 10.1007/s00702-005-0328-y.

Gilks, W.P. and Abou-Sleiman, P.M. and Gandhi, S. and Jain, S. and Singleton, A. and Lees, A.J. and Shaw, K. and Bhatia, K.P. and Bonifati, V. and Quinn, N.P. and Lynch, J. and Healy, D.G. and Holton, J.L. and Revesz, T. and Wood, N.W. (2005) A common LRRK2 mutation in idiopathic Parkinson's disease. The Lancet , 365 (9457) pp. 415-416. 10.1016/S0140-6736(05)17830-1.

Gilks, WP and Abou-Sleiman, PM and Gandhi, S and Jain, S and Singleton, A and Lees, AJ and Shaw, K and Bhatia, KP and Bonifati, V and Quinn, NP and Lynch, J and Healy, DG and Holton, JL and Revesz, T and Wood, NW (2005) Common LRRK2 mutation in idiopathic Parkinson's disease. LANCET , 365 (9457) 415 - 416.

Gioltzoglou, T and Cordivari, C and Lee, PJ and Hanna, MG and Lees, AJ (2005) Problems with botulinum toxin treatment in mitochondrial cytopathy: case report and review of the literature. J NEUROL NEUROSUR PS , 76 (11) 1594 - 1596. 10.1136/jnnp.2004.057661.

Godbolt, AK and Josephs, KA and Revesz, T and Warrington, EK and Lantos, P and King, A and Fox, NC and Al Sarraj, S and Holton, J and Cipolotti, L and Khan, MN and Rossor, MN (2005) Sporadic and familial dementia with ubiquitin-positive tau-negative inclusions - Clinical features of one histopathological abnormality underlying frontotemporal lobar degeneration. ARCH NEUROL-CHICAGO , 62 (7) 1097 - 1101.

Graves, T and Imbrici, P and Eunson, L and Bhatia, KP and Wodia, NH and Hanna, MG and Kullmann, DM (2005) Late onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 156 - 157). B M J PUBLISHING GROUP

Graves, TD and Hanna, MG (2005) Neurological channelopathies. POSTGRAD MED J , 81 (951) 20 - 32. 10.1136/pgmj.2004.022012.
An open access publication

H

Hanna, MG and Cudia, P (2005) Peripheral nerve diseases associated with mitochondrial respiratory chain dysfunction. In: Dyck, PJ and Thomas, PK, (eds.) Peripheral neuropathy. (1937 - 1949). Elsevier Saunders: Philadelphia.

Hanna, MG and Graves, TD and Jaffe, S and Imbrici, P and Kullmann, DM (2005) Dysfunction of the brain calcium channel Ca(V)2.1 in absence epilepsy and episodic ataxia - authors' response. BRAIN , 128 ? - ?. 10.1093/brain/awh439.

Hardy, J (2005) Expression of normal sequence pathogenic proteins for neurodegenerative disease contributes to disease risk: 'permissive templating' as a general mechanism underlying neurodegeneration. In: BIOCHEMICAL SOCIETY TRANSACTIONS. (pp. 578 - 581).

Hardy, J and Lees, AJ (2005) Parkinson's disease: A broken nosology. MOVEMENT DISORDERS , 20 S2 - S4. 10.1002/mds.20532.

Hardy, J and Pittman, A and Myers, A and Gwinn-Hardy, K and Fung, HC and de Silva, R and Hutton, M and Duckworth, J (2005) Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens. BIOCHEMICAL SOCIETY TRANSACTIONS , 33 582 - 585.

Healy, DG and Abou-Sleiman, PM and Quinn, N and Ahmadi, KR and Ozawa, T and Kamm, C and Wullner, U and Oertel, WH and Burk, K and Dupont, E and Pellecchia, MT and Tolosa, E and Gasser, T and Holton, JL and Revesz, T and Goldstein, DB and Lees, AJ and Wood, NW and European MSA Study Grp, (2005) UCHL-1 gene in multiple system atrophy: A haplotype tagging approach. MOVEMENT DISORD , 20 (10) 1338 - 1343. 10.1002/mds.20575.

Henley, SM and Warner, TT and Warrington, EK and Stevens, JM and Ashburner, J and Fox, NC (2005) Longitudinal changes in MRI and neuropsychological measures in early Huntington's disease - A pilot study. In: MOVEMENT DISORDERS. (pp. S9 - S9). WILEY-LISS

Henley, SMD and Warrington, EK and Frost, C and MacManus, DG and Warner, TT and Fox, NC and Tabrizi, SJ (2005) Mri and cognitive changes detectable over 6 and 12 months in early Huntington's disease. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. ? - ?). B M J PUBLISHING GROUP

Hernandez, D and Paisan Ruiz, C and Crawley, A and Malkani, R and Werner, J and Gwinn-Hardy, K and Dickson, D and Wavrant Devrieze, F and Hardy, J and Singleton, A (2005) The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases. Neurosci Lett , 389 (3) 137 - 139. 10.1016/j.neulet.2005.07.044.

Hernandez, DG and Paisan-Ruiz, C and McInerney-Leo, A and Jain, S and Meyer-Lindenberg, A and Evans, EW and Berman, KF and Johnson, J and Auburger, G and Schaffer, AA and Lopez, GJ and Nussbaum, RL and Singleton, AB (2005) Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. ANN NEUROL , 57 (3) 453 - 456. 10.1002/ana.20401.

Holmans, P and Hamshere, M and Hollingworth, P and Rice, F and Tunstall, N and Jones, S and Moore, P and DeVrieze, FW and Myers, A and Crook, R and Compton, D and Marshall, H and Meyer, D and Shears, S and Booth, J and Ramic, D and Williams, N and Norton, N and Abraham, R and Kehoe, P and Williams, H and Rudrasingham, V and O'Donovan, M and Jones, L and Hardy, J and Goate, A and Lovestone, S and Owen, M and Williams, J (2005) Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 135B (1) 24 - 32. 10.1002/ajmg.b.30114.

Holton, JL and Revesz, T and Bhardwaj, N and Venner, K and Vicart, P and Goldfarb, L and Clarke, C (2005) A novel desmin mutation associated with skeletal myopathy and heart block. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 239 - 239). BLACKWELL PUBLISHING LTD

Houlden, H and King, RHM and Blake, J and Jacobs, J and Groves, MJ and Love, S and Woodward, C and Hammons, S and Nicoll, J and Thomas, PK and Reilly, MM (2005) Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I). In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. 35 - 35). BLACKWELL PUBLISHING

Houlden, H and Roper, H and Blake, J and Reilly, MM (2005) Manifesting carriers and genetic heterogeneity in giant axonal neuropathy. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. 35 - 35). BLACKWELL PUBLISHING

Huang, CS and Shi, SH and Ule, J and Ruggiu, M and Barker, LA and Darnell, RB and Jan, YN and Jan, LY (2005) Common molecular pathways mediate long-term potentiation of synaptic excitation and slow synaptic inhibition. Cell , 123 105 - 118.

I

Ibrahim, A and Galloway, M and Leung, C and Revesz, T and Crockard, A (2005) Cervical spine chordoid meningioma - Case report. J NEUROSURG-SPINE , 2 (2) 195 - 198.

Imbrici, P and Eunson, LH and Graves, TD and Bhatia, KP and Wadia, NH and Kullmann, DM and Hanna, MG (2005) Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A. NEUROLOGY , 65 (6) 944 - 946.

Iwata, O. and Thornton, J.S. and Sellwood, M.W. and Iwata, S. and Sakata, Y. and Noone, M.A. and O’Brien, F.E. and Bainbridge, A. and De Vita, E. and Raivich, G. and Peebles, D. and Scaravilli, F. and Cady, E.B. and Ordidge, R. and Wyatt, J.S. and Robertson, N.J. (2005) Depth of delayed cooling alters neuroprotection pattern after hypoxia-ischemia. Annals of Neurology , 58 (1) pp. 75-87. 10.1002/ana.20528.

J

Jain, S and Wood, NW and Healy, DG (2005) Molecular genetic pathways in Parkinson's disease: a review. CLIN SCI , 109 (4) 355 - 364. 10.1042/CS0050106.

Jain, S and Wood, NW and Healy, DG (2005) Molecular genetic pathways in Parkinson's disease: a review. Clin Sci (Lond) , 109 (4) 355 - 364. 10.1042/CS20050106.

K

Kamm, C and Healy, DG and Quinn, NP and Wullner, U and Moller, JC and Schols, L and Geser, F and Burk, K and Borglum, AD and Pellecchia, MT and Tolosa, E and del Sorbo, F and Nilsson, C and Bandmann, O and Sharma, M and Mayer, P and Gasteiger, M and Haworth, A and Ozawa, T and Lees, AJ and Short, J and Giunti, P and Holinski-Feder, E and Illig, T and Wichmann, HE and Wenning, GK and Wood, NW and Gasser, T and EMSA Study Grp, (2005) The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group. BRAIN , 128 1855 - 1860. 10.1093/brain/awh535.

Kennard, C and Mannan, SK and Nachev, P and Parton, A and Mort, DJ and Rees, G and Hodgson, TL and Husain, M (2005) Cognitive processes in saccade generation. In: Ramat, S and Straumann, D, (eds.) CLINICAL AND BASIC OCULOMOTOR RESEARCH: IN HONOR OF DAVID S. ZEE. (pp. 176 - 183). NEW YORK ACAD SCIENCES

Khan, NL and Giunti, P and Sweeney, MG and Scherfler, C and Brien, MO and Piccini, P and Wood, NW and Lees, AJ (2005) Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6). MOVEMENT DISORD , 20 (9) 1115 - 1119. 10.1002/mds.20564.

Khan, NL and Horta, W and Eunson, L and Graham, E and Johnson, JO and Chang, S and Davis, M and Singleton, A and Wood, NW and Lees, AJ (2005) Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years. MOVEMENT DISORD , 20 (4) 479 - 484. 10.1002/mds.20335.

Khan, NL and Jain, S and Lynch, JM and Pavese, N and Abou-Sleiman, P and Holton, JL and Healy, DG and Gilks, WP and Sweeney, MG and Ganguly, M and Gibbons, V and Gandhi, S and Vaughan, J and Eunson, LH and Katzenschlager, R and Gayton, J and Lennox, G and Revesz, T and Nicholl, D and Bhatia, KP and Quinn, N and Brooks, D and Lees, AJ and Davis, MB and Piccini, P and Singleton, AB and Wood, NW (2005) Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data. BRAIN , 128 2786 - 2796. 10.1093/brain/awh667.

Khan, NL and Scherfler, C and Graham, E and Bhatia, KP and Quinn, N and Lees, AJ and Brooks, DJ and Wood, NW and Piccini, P (2005) Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation. NEUROLOGY , 64 (1) 134 - 136.

Kumar-Singh, S and Pirici, D and McGowan, E and Serneels, S and Ceuterick, C and Hardy, J and Duff, K and Dickson, D and Van Broeckhoven, C (2005) Dense-core plaques in Tg2576 and PSAPP mouse models of Alzheimer's disease are centered on vessel walls. AMERICAN JOURNAL OF PATHOLOGY , 167 (2) 527 - 543. 10.1016/S0002-9440(10)62995-1.

Kuo, LT and Simpson, A and Schanzer, A and Tse, J and An, SF and Scaravilli, F and Groves, MJ (2005) Effects of systemically administered NT-3 on sensory neuron loss and nestin expression following axotomy. J COMP NEUROL , 482 (4) 320 - 332. 10.1002/cne.20400.

L

Lahiri, DK and Ge, YW and Maloney, B and Wavrant-De Vrieze, F and Hardy, J (2005) Characterization of two APP gene promoter polymorphisms that appear to influence risk of late-onset Alzheimer's disease. NEUROBIOLOGY OF AGING , 26 (10) 1329 - 1341. 10.1016/j.neurobiolaging.2004.11.005.

Lashley, T and Holton, JL and Frangione, B and van Horssen, J and Rostagno, A and Verbeek, MM and Ghiso, J and Revesz, T (2005) Amyloid-associated proteins (AAPs) in familial British dementia (FBD) and familial Danish dementia (FDD). In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 244 - 244). BLACKWELL PUBLISHING LTD

Lee, CCM and Kuo, LT and Wang, CH and Scaravilli, F and An, SF (2005) Accumulation of prion protein in the peripheral nervous system in human prion diseases. J NEUROPATH EXP NEUR , 64 (8) 716 - 721.

Li, C and Holton, JL and Varsani, H and Weaver, N and Harding, B and Woo, P and Wedderburn, LR (2005) Initial histological features in juvenile dermatomyositis may predict clinical progression. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 230 - 230). BLACKWELL PUBLISHING LTD

Li, CKC and Holton, JL and Varsani, H and Woo, P and Wedderburn, LR (2005) Histological features in juvenile dermatomyositis may predict clinical progression. In: RHEUMATOLOGY. (pp. I92 - I93). OXFORD UNIV PRESS

Li, Y and Rowland, C and Tacey, K and Catanese, J and Sninsky, J and Hardy, J and Powell, J and Lovestone, S and Morris, JC and Thal, L and Goate, A and Owen, M and Williams, J and Grupe, A (2005) The BDNF val66met polymorphism is not associated with late onset Alzheimer's disease in three case-control samples. MOLECULAR PSYCHIATRY , 10 (9) 809 - 810. 10.1038/sj.mp.4001702.

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This list was generated on Tue May 21 08:42:33 2013 BST.