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Number of items: 148.
A
| Abramov, AY and Fraley, C and Diao, CT and Winkfein, R and Colicos, MA and Duchen, MR and French, RJ and Pavlov, E (2007) Targeted polyphosphatase expression alters mitochondrial metabolism and inhibits calcium-dependent cell death. P NATL ACAD SCI USA , 104 (46) 18091 - 18096. 10.1073/pnas.0708959104. |
| Abramov, AY and Scorziello, A and Duchen, MR (2007) Three distinct mechanisms generate oxygen free radicals in neurons and contribute to cell death during anoxia and reoxygenation. J NEUROSCI , 27 (5) 1129 - 1138. 10.1523/JNEUROSCI.4468-06.2007. |
B
| Bar, H and Goudeau, B and Walde, S and Casteras-Simon, M and Mucke, N and Shatunov, A and Goldberg, YP and Clarke, C and Holton, JL and Eymard, B and Katus, HA and Fardeau, M and Goldfarb, L and Vicart, P and Herrmann, H (2007) Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathies. HUM MUTAT , 28 (4) 374 - 386. 10.1002/humu.20459. |
| Bennett, DLH and Groves, M and Blake, J and Holton, JL and King, RHM and Orrell, RW and Ginsberg, L and Reilly, MM (2007) The use of nerve and muscle biopsy in the diagnosis of vasculitis: a 5-year retrospective study of 53 cases. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. 9 - 10). BLACKWELL PUBLISHING |
| Bettencourt, C and Silva-Fernandes, A and Montiel, R and Santos, C and Maciel, P and Lima, M (2007) Triplet Repeats: Features, Dynamics and Evolutionary Mechanisms. In: Santos, C and Lima, M, (eds.) Recent Advances in Molecular Biology and Evolution: Applications to Biological Anthropology. (83 - 114). Research Signpost: Kerala. |
| Bowen, S and Ateh, DD and Deinhardt, K and Bird, MM and Price, KM and Baker, CS and Robson, JC and Swash, M and Shamsuddin, W and Kawar, S and El-Tawil, T and Roos, J and Hoyle, A and Nickols, CD and Knowles, CH and Pullen, AH and Luthert, PJ and Weller, RO and Hafezparast, M and Franklin, RJM and Revesz, T and King, RHM and Berninghausen, O and Fisher, EMC and Schiavo, G and Martin, JE (2007) The phagocytic capacity of neurones. EUR J NEUROSCI , 25 (10) 2947 - 2955. 10.1111/j.1460-9568.2007.05554.x. |
| Broderick, P and Carvajal-Carmona, L and Pittman, AM and Webb, E and Howarth, K and Rowan, A and Lubbe, S and Spain, S and Sullivan, K and Fielding, S and Jaeger, E and Vijayakrishnan, J and Kemp, Z and Gorman, M and Chandler, I and Papaemmanuil, E and Penegar, S and Wood, W and Sellick, G and Qureshi, M and Teixeira, A and Domingo, E and Barclay, E and Martin, L and Sieber, O and CORGI Consortium, and Kerr, D and Gray, R and Peto, J and Cazier, JB and Tomlinson, I and Houlston, RS (2007) A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. Nat Genet , 39 (11) 1315 - 1317. 10.1038/ng.2007.18. |
| Brown, AM and Gordon, D and Lee, H and Vrieze, FW-D and Cellini, E and Bagnoli, S and Nacmias, B and Sorbi, S and Hardy, J and Blass, JP (2007) Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations. NEUROCHEMICAL RESEARCH , 32 (4-5) 857 - 869. 10.1007/s11064-006-9235-3. |
| Bruni, AC and Momeni, P and Bernardi, L and Tomaino, C and Frangipane, F and Elder, J and Kawarai, T and Sato, C and Pradella, S and Wakutani, Y and Anfossi, M and Gallo, M and Geracitano, S and Costanzo, A and Smirne, N and Curcio, SAM and Mirabelli, M and Puccio, G and Colao, R and Maletta, RG and Kertesz, A and St George-Hyslop, P and Hardy, J and Rogaeva, E (2007) Heterogeneity within a large kindred with frontotemporal dementia - A novel progranulin mutation. NEUROLOGY , 69 (2) 140 - 147. 10.1212/01.wnl.0000265220.64396.b4. |
| Bullmann, T and de Silva, R and Holzer, M and Mori, H and Arendt, T (2007) Expression of embryonic tau protein isoforms persist during adult neurogenesis in the hippocampus. HIPPOCAMPUS , 17 (2) 98 - 102. 10.1002/hipo.20255. |
| Bullmann, T and de Silva, R and Holzer, M and Mori, H and Arendt, T (2007) The adult rodent hippocampus as a model for studying shifts in tau isoform expression. In: JOURNAL OF NEURAL TRANSMISSION. (pp. CXXIII - CXXIII). SPRINGER WIEN |
C
| Cano, SJ and Thompson, AJ and Bhatia, K and Fitzpatrick, R and Warner, TT and Hobart, JC (2007) Evidence-based guidelines for using the short form 36 in cervical dystonia. MOVEMENT DISORD , 22 (1) 122 - 126. 10.1002/mds.21187. |
| Cano, SJ and Warner, TT (2007) Dystonia and quality of life. In: Warner, TT and Bressman, SB, (eds.) Clinical diagnosis and management of dystonia. (241 - 248). Informa healthcare: London. |
| Cano, SJ and Warner, TT (2007) Dystonia rating scales. In: Warner, TT and Bressman, SB, (eds.) Clinical diagnosis and management of dystonia. (249 - 260). Informa healthcare: London. |
| Cavalleri, GL and Walley, NM and Soranzo, N and Mulley, J and Doherty, CP and Kapoor, A and Depondt, C and Lynch, JM and Scheffer, IE and Heils, A and Gehrmann, A and Kinirons, P and Gandhi, S and Satishchandra, P and Wood, NW and Anand, A and Sander, T and Berkovic, SF and Delanty, N and Goldstein, DB and Sisodiya, SM (2007) A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy. EPILEPSIA , 48 (4) 706 - 712. 10.1111/j.1528-1167.2007.00977.x. |
| Cavalleri, GL and Weale, ME and Shianna, KV and Singh, R and Lynch, JM and Grinton, B and Szoeke, C and Murphy, K and Kinirons, P and O'Rourke, D and Ge, D and Depondt, C and Claeys, KG and Pandolfo, M and Gumbs, C and Walley, N and McNamara, J and Mulley, JC and Linney, KN and Sheffield, LJ and Radtke, RA and Tate, SK and Chissoe, SL and Gibson, RA and Hosford, D and Stanton, A and Graves, TD and Hanna, MG and Eriksson, K and Kantanen, AM and Kalviainen, R and O'Brien, TJ and Sander, JW and Duncan, JS and Scheffer, IE and Berkovic, SF and Wood, NW and Doherty, CP and Delanty, N and Sisodiya, SM and Goldstein, DB (2007) Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study. LANCET NEUROL , 6 (11) 970 - 980. 10.1016/Sl474-4422(07)70247-8. |
| Chen, KW and Reiman, EM and Alexander, GE and Caselli, RJ and Gerkin, R and Bandy, D and Domb, A and Osborne, D and Fox, N and Crum, WR and Saunders, AM and Hardy, J (2007) Correlations between apolipoprotein E epsilon 4 gene dose and whole brain atrophy rates. In: AMERICAN JOURNAL OF PSYCHIATRY. (pp. 916 - 921). AMER PSYCHIATRIC PUBLISHING, INC |
| Chinnery, PF and Hudson, G and Stewart, J and Craig, K and Taylor, RW and Turnbull, DM and Ramesh, V and McFarland, R and Burn, DJ and Hanna, MG and Horvath, R and Lochmueller, H and Zeviani, M (2007) When and how should neurologists test for mutations in POLG? In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 1014 - 1014). B M J PUBLISHING GROUP |
| Coon, KD and Myers, AJ and Craig, DW and Webster, JA and Pearson, JV and Lince, DH and Zismann, VL and Beach, TG and Leung, D and Bryden, L and Halperin, RF and Marlowe, L and Kaleem, M and Walker, DG and Ravid, R and Heward, CB and Rogers, J and Papassotiropoulos, A and Reiman, EM and Hardy, J and Stephan, DA (2007) A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. JOURNAL OF CLINICAL PSYCHIATRY , 68 (4) 613 - 618. |
| Craig, K and Elliott, HR and Keers, SM and Lambert, C and Pyle, A and Graves, TD and Woodward, C and Sweeney, MG and Davis, MB and Hanna, MG and Chinnery, PF (2007) Episodic ataxia and hemiplegia caused by the 8993T -> C mitochondrial DNA mutation. JOURNAL OF MEDICAL GENETICS , 44 (12) 797 - 799. 10.1136/jmg.2007.052902. |
D
| De Ferrari, GV and Papassotiropoulos, A and Biechele, T and De-Vrieze, FW and Avila, ME and Major, MB and Myers, A and Saez, K and Henriquez, JP and Zhao, A and Wollmer, MA and Nitsch, RM and Hock, C and Morris, CM and Hardy, J and Moon, RT (2007) Common genetic variation within the Low-Density Lipoprotein Receptor-Related Protein 6 and late-onset Alzheimer's disease. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , 104 (22) 9434 - 9439. 10.1073/pnas.0603523104. |
| Devine, ME and Fonseca, JAS and Walker, RWH and Sikdar, T and Stevens, T and Walker, Z (2007) Cerebral white matter changes and rate of progression of dementia during cholinesterase inhibitor treatment: a retrospective cohort study. INT J GERIATR PSYCH , 22 (11) 1120 - 1126. 10.1002/gps.1799. |
| Devine, MJ and Duncan, JS (2007) Development of psychogenic non-epileptic seizures in response to auditory hallucinations. SEIZURE-EUR J EPILEP , 16 (8) 717 - 721. 10.1016/j.seizure.2007.06.001. |
| Duff, K and Paulsen, JS and Beglinger, LJ and Langbehn, DR and Stout, JC and Investigators, P-H (2007) Psychiatric symptoms in Huntington's disease before diagnosis: The Predict-HD study. BIOLOGICAL PSYCHIATRY , 62 (12) 1341 - 1346. 10.1016/j.biopsych.2006.11.034. |
| Duke, VM and Gurunlian, N and Yogashangari, B and Colley, T and McNamara, C and Hoffbrand, AV and Foroni, L (2007) Frequency of JAK2 exon 12 mutations in JAK2 exon 14 V617F-negative patients: High frequency in ET patients. In: BLOOD. (pp. 748A - 748A). AMER SOC HEMATOLOGY |
F
| Fialho, D and Hanna, MG (2007) Periodic paralysis. In: UNSPECIFIED (77 - 106). |
| Fialho, D and Schorge, S and Pucovska, U and Davies, NP and Labrum, R and Haworth, A and Stanley, E and Sud, R and Wakeling, W and Davis, MB and Kullmann, DM and Hanna, MG (2007) Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions. BRAIN , 130 3265 - 3274. 10.1093/brain/awm248. |
| Fidani, L and Clarimon, J and Goulas, A and Hatzitolios, AI and Evans, W and Tsirogianni, E and Hardy, J and Kotsis, A (2007) Association of phosphodiesterase 4D gene G0 haplotype and ischaemic stroke in a Greek population. EUROPEAN JOURNAL OF NEUROLOGY , 14 (7) 745 - 749. 10.1111/j.1468-1331.2007.01767.x. |
| Fung, Hon Chung (2007) Genetic Characterisation of Neurodegenerative disorders. Doctoral thesis, University of London. |  |
G
| Galloway, M and Amin, A and Casey, A and Crockard, A and Revesz, T (2007) Smear cytology in the intra-operative assessment of periodontoid pseudotumour of the craniocervical junction. CYTOPATHOLOGY , 18 (6) 388 - 390. 10.1111/j.1365-2303.2006.00398.x. |
| Giunti, P (2007) The Ataxia Centre at the NHNN: A year experience. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 218 - 218). B M J PUBLISHING GROUP |
| Giunti, P and Gray, J and Wood, NW (2007) A phase III double blind, randomised, placebo controlled study of the efficacy, safety and tolerability of idebenone in the treatment of Friedreich's ataxia patients. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 1026 - 1026). B M J PUBLISHING GROUP |
| Giunti, P and Gray, J and Wood, NW (2007) A phase III double-blind, randomised, placebo-controlled study of the efficacy, safety and tolerability of idebenone in the treatment of Friedreich's ataxia patients. In: MOVEMENT DISORDERS. (pp. S12 - S12). WILEY-LISS |
| Giunti, P and Wood, N (2007) The inherited ataxias. ACNR , 7 (5) 18 - 21. |
| Goldstein, DS and Imrich, R and Peckham, E and Holmes, C and Lopez, G and Crews, C and Hardy, J and Singleton, A and Hallett, M (2007) Neurocirculatory and nigrostriatal abnormalities in Parkinson disease from LRRK2 mutation. NEUROLOGY , 69 (16) 1580 - 1584. 10.1212/01.wnl.0000268696.57912.64. |
| Gonzalez, AM and Moriyama, LS and Williams, DR and O'Sullivan, S and Massey, LA and Da Silva, R and Holton, JL and Lees, AJ (2007) A combined case of tauopathy and Alpha-synucleinopathy. In: MOVEMENT DISORDERS. (pp. S256 - S256). WILEY-LISS |
| Goold, R and Hubank, M and Hunt, A and Holton, J and Menon, RP and Revesz, T and Pandolfo, M and Matilla-Duenas, A (2007) Down-regulation of the dopamine receptor D2 in mice lacking ataxin 1. HUM MOL GENET , 16 (17) 2122 - 2134. 10.1093/hmg/ddm162. |
| Granata, A and Schiavo, G and Warner, TT (2007) The dystonia-associated protein torsinA modulates synaptic vesicle recycling. In: MOVEMENT DISORDERS. (pp. S4 - S5). |
| Graves, TD and Kullmann, DM and Hanna, MG (2007) Episodic ataxia type 2 (EA2) is associated with epilepsy. In: NEUROLOGY. (pp. A80 - A80). LIPPINCOTT WILLIAMS & WILKINS |
| Graves, TD and Schorge, S and Morris, H and Kullmann, DM and Hanna, MG (2007) A novel voltage-sensing mutation in Kv1.1 is associated with episodic ataxia type 1. In: JOURNAL OF NEUROLOGY. (pp. 28 - 29). DR DIETRICH STEINKOPFF VERLAG |
| Graves, TD and Zuberi, SM and Schorge, S and Kullmann, DM and Hanna, MG (2007) A clinical, genetic and electrophysiological study of a new UK episodic ataxia type 1 (EA1) pedigree. In: NEUROLOGY. (pp. A253 - A253). LIPPINCOTT WILLIAMS & WILKINS |
| Graves, TD and Zuberi, SM and Schorge, S and Kullmann, DM and Hanna, MG (2007) A clinical, genetic and electrophysiological study of a new UK episodic ataxia type 1 pedigree. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 1019 - 1019). B M J PUBLISHING GROUP |
| Greggio, E and Lewis, PA and van der Brug, MP and Ahmad, R and Kaganovich, A and Ding, JH and Beilina, A and Baker, AK and Cookson, MR (2007) Mutations in LRRK2/dardarin associated with Parkinson disease are more toxic than equivalent mutations in the homologous kinase LRRK1. J NEUROCHEM , 102 (1) 93 - 102. 10.1111/j.1471-4159.2007.04523.x. |
| Guerreiro, RJ and Santana, I and Bras, JM and Santiago, B and Paiva, A and Oliveira, C (2007) Peripheral inflammatory Cytokines as biomarkers in Alzheimer's disease and mild cognitive impairment. NEURODEGENER DIS , 4 (6) 406 - 412. 10.1159/000107700. |
| Gwinn, K and Corriveau, RA and Mitsumoto, H and Bednarz, K and Jr, BRH and Cudkowicz, M and Gordon, PH and Hardy, J and Kasarskis, EJ and Kaufmann, P and Miller, R and Sorenson, E and Tandan, R and Traynor, BJ and Nash, J and Sherman, A and Mailman, MD and Ostell, J and Bruijn, L and Cwik, V and Rich, SS and Singleton, A and Refolo, L and Andrews, J and Zhang, R and Conwit, R and Keller, MA and Grp, ALSR (2007) Amyotrophic Lateral Sclerosis: An Emerging Era of Collaborative Gene Discovery. PLOS ONE , 2 (12) , Article e1254. 10.1371/journal.pone.0001254. | |
H
| Hamshere, ML and Holmans, PA and Avramopoulos, D and Bassett, SS and Blacker, D and Bertram, L and Wiener, H and Rochberg, N and Tanzi, RE and Myers, A and Vrieze, FWD and Go, R and Fallin, D and Lovestone, S and Hardy, J and Goate, A and O'Donovan, M and Williams, J and Owen, MJ (2007) Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. HUM MOL GENET , 16 (22) 2703 - 2712. 10.1093/hmg/ddm224. |
| Hanger, DP and Byers, HL and Wray, S and Leung, KY and Saxton, MJ and Seereeram, A and Reynolds, CH and Ward, MA and Anderton, BH (2007) Novel phosphorylation sites in tau from Alzheimer brain support a role for casein kinase 1 in disease pathogenesis. J Biol Chem , 282 (32) 23645 - 23654. 10.1074/jbc.M703269200. |
| Hanna, M and Graves, T and Kullmann, D (2007) Discussion. Epileptic Disorders , 9 (2) 215 - 216. |
| Hardy, J (2007) Does A beta 42 have a function related to blood homeostasis? NEUROCHEMICAL RESEARCH , 32 (4-5) 833 - 835. 10.1007/s11064-006-9221-9. |
| Hardy, J (2007) Putting presenilins centre stage - Introduction to the Talking Point on the role of presenilin mutations in Alzheimer disease. EMBO REPORTS , 8 (2) 134 - 135. 10.1038/sj.embor.7400899. |
| Hardy, J and Myers, A (2007) Genetic variability in expression of proteins and the risk of sporadic neurologic diseases. NEUROLOGY , 68 (9) 632 - 633. 10.1212/01.wnl.0000256793.58438.c4. |
| Hardy, J and Singleton, A (2007) Reporting and interpretation of genetic variants in cases and controls. NEUROLOGY , 69 (1) 111 - 112. 10.1212/01.wnl.0000265059.56575.a6. |
| Haubenberger, D and Bonelli, S and Hotzy, C and Leitner, P and Lichtner, P and Samal, D and Katzenschlager, R and Djamshidian, A and Brucke, T and Steffelbauer, M and Bancher, C and Grossmann, J and Ransmayr, G and Strom, TM and Meitinger, T and Gasser, T and Auff, E and Zimprich, A (2007) A novel LRRK2 mutation in an austrian cohort of patients with Parkinson's disease. MOVEMENT DISORD , 22 (11) 1640 - 1643. 10.1002/mds.21568. |
| Heinzen, EL and Yoon, W and Tate, SK and Sen, A and Wood, NW and Sisodiya, SM and Goldstein, DB (2007) Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug-responsive splice variants of SCN1A. AM J HUM GENET , 80 (5) 876 - 883. 10.1086/516650. |
| Heinzen, EL and Yoon, W and Weale, ME and Sen, A and Wood, NW and Burke, JR and Welsh-Bohmer, KA and Hulette, CM and Sisodiya, SM and Goldstein, DB (2007) Alternative ion channel splicing in mesial temporal lobe epilepsy and Alzheimer's disease. GENOME BIOL , 8 (3) , Article R32. 10.1186/gb-2007-8-3-r32. |
| Hodgetts, A and Levin, M and Kroll, JS and Langford, PR (2007) Biomarker discovery in infectious diseases using SELDI. FUTURE MICROBIOL , 2 (1) 35 - 49. 10.2217/17460913.2.1.35. |
| Hollingworth, P and Hamshere, ML and Holmans, PA and O'Donovan, MC and Sims, R and Powell, J and Lovestone, S and Myers, A and DeVrieze, FW and Hardy, J and Goate, A and Owen, M and Williams, J (2007) Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 144B (7) 841 - 848. 10.1002/ajmg.b.30515. |
| Holton, JL and Schneider, SA and Gandhi, S and Ganesharajah, T and Strand, C and Shashidharan, P and Barreto, J and Wood, NW and Lees, AJ and Bhatia, KP and Revesz, T (2007) Neuropathology of primary dystonia unrelated to DYT1 mutations. In: MOVEMENT DISORDERS. (pp. S114 - S114). WILEY-LISS |
| Houlden, H and Charlton, P and Singh, D (2007) Neurology and orthopaedics. J NEUROL NEUROSUR PS , 78 (3) 224 - 232. 10.1136/jnnp.2006.092072. |
| Houlden, H and Groves, M and Miedzybrodzka, Z and Roper, H and Willis, T and Winer, J and Cole, G and Reilly, MM (2007) New mutations, genotype phenotype studies and manifesting carriers in giant axonal neuropathy. J NEUROL NEUROSUR PS , 78 (11) 1267 - 1270. 10.1136/jnnp.2007.118968. |
| Houlden, H and Johnson, J and Gardner-Thorpe, C and Lashley, T and Hernandez, D and Worth, P and Singleton, AB and Hilton, DA and Holton, J and Revesz, T and Davis, MB and Giunti, P and Wood, NW (2007) Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11. NAT GENET , 39 (12) 1434 - 1436. 10.1038/ng.2007.43. |
J
| Jelen, N and Ule, J and Zivin, M and Darnell, RB (2007) Evolution of Nova-dependent splicing regulation in the brain. PLoS Genet , 3 1838 - 1847. |
| Jen, JC and Graves, TD and Hess, EJ and Hanna, MG and Griggs, RC and Baloh, RW and CINCH investigators, (2007) Primary episodic ataxias: diagnosis, pathogenesis and treatment. In: BRAIN. (pp. 2484 - 2493). OXFORD UNIV PRESS |
| Johnson, J and Paisan-Ruiz, C and Lopez, G and Crews, C and Britton, A and Malkani, R and Evans, EW and McInerney-Leo, A and Jain, S and Nussbaum, RL and Foote, KD and Mandel, RJ and Crawley, A and Reimsnider, S and Fernandez, HH and Okun, MS and Gwinn-Hardy, K and Singleton, AB (2007) Comprehensive screening of a north American Parkinson's disease cohort for LRRK2 mutation. NEURODEGENER DIS , 4 (5) 386 - 391. 10.1159/000105160. |
K
| Kasperaviciute, D and Weale, ME and Shianna, KV and Banks, GT and Simpson, CL and Hansen, VK and Turner, MR and Shaw, CE and Al-Chalabi, A and Pall, HS and Goodall, EF and Morrison, KE and Orrell, RW and Beck, M and Jablonka, S and Sendtner, M and Brockington, A and Ince, PG and Hartley, J and Nixon, H and Shaw, PJ and Schiavo, G and Wood, NW and Goldstein, DB and Fisher, EMC (2007) Large-scale pathways-based association study in amyotrophic lateral sclerosis. BRAIN , 130 2292 - 2301. 10.1093/brain/awm055. |
| Katzenschlager, R. and Schrag, A. and Evans, A. and Manson, A. and Carroll, C.B. and Ottaviani, D. and Lees, A.J. and Hobart, J. (2007) Quantifying the impact of dyskinesias in PD: the PDYS-26: A patient-based outcome measure. Neurology , 69 (6) pp. 555-563. 10.1212/01.wnl.0000266669.18308.af. |
| Kempster, PA and Williams, DR and Selikhova, M and Holton, J and Revesz, T and Lees, AJ (2007) Patterns of levodopa response in Parkinson's disease: a clinico-pathological study. Brain , 130 (Pt 8) 2123 - 2128. 10.1093/brain/awm142. |
| Kerr, JR and Christian, P and Hodgetts, A and Langford, PR and D Devanur, L and Petty, R and Burke, B and Sinclair, LI and Richards, SCM and Montgomery, J and McDermott, CR and Harrison, TJ and Kellam, P and Nutt, DJ and Holgate, ST and Clinical Study Grp, (2007) Current research priorities in chronic fatigue syndrome/myalgic encephalomyelitis: disease mechanisms, a diagnostic test and specific treatments. J CLIN PATHOL , 60 (2) 113 - 116. 10.1136/jcp.2006.042374. | |
| Kerr, JR and Christian, P and Hodgetts, A and Langford, PR and Devanur, LD and Petty, R and Burke, B and Sinclair, LI and Richards, SC and Montgomery, J and McDermott, CR and Harrison, TJ and Kellam, P and Nutt, DJ and Holgate, ST and Collaborative Clinical Study Group, (2007) Current research priorities in chronic fatigue syndrome/myalgic encephalomyelitis: disease mechanisms, a diagnostic test and specific treatments. J Clin Pathol , 60 (2) 113 - 116. 10.1136/jcp.2006.042374. |
| Kerr, JR and Christian, P and Hodgetts, A and Langford, PR and Devanur, LD and Petty, R and Burke, B and Sinclair, LI and Richards, SCM and Montgomery, J and McDermott, CR and Harrison, TJ and Kellam, P and Nutt, DJ and Holgate, ST and Honeybourne, D and Smith, AP and Thomas, M and Ayres, JG and Main, J and Daymond, T and Bansal, A and Puri, BK and Morgan, R and Peveler, RC and Axford, JS and Weir, W and Enlander, D and Chia, JK (2007) Current research priorities in chronic fatigue syndrome/myalgic encephalomyelitis: Disease mechanisms, a diagnostic test and specific treatments. Journal of Clinical Pathology , 60 (2) 113 - 116. |
| Khan, NL and Bhatt, M and Brooks, DJ and Korlipara, P and Schapira, A and Piccini, P and Wood, NW and Bhatia, K (2007) An Indian kindred with reversible dystonia and parkinsonism. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 210 - 210). B M J PUBLISHING GROUP |
| Kumaran, R and Kingsbury, A and Coulter, I and Lashley, T and Williams, D and de Silva, R and Mann, D and Revesz, T and Lees, A and Bandopadhyay, R (2007) DJ-1 (PARK7) is associated with 3R and 4R tau neuronal and glial inclusions in neurodegenerative disorders. NEUROBIOL DIS , 28 (1) 122 - 132. 10.1016/j.nbd.2007.07.012. |
| Kuo, LT and Groves, MJ and Scaravilli, F and Sugden, D and An, SF (2007) Neurotrophin-3 administration alters neurotrophin, neurotrophin receptor and nestin mRNA expression in rat dorsal root ganglia following axotomy. NEUROSCIENCE , 147 (2) 491 - 507. 10.1016/j.neuroscience.2007.04.023. |
L
| Lace, G and Ince, PG and Matthews, F and Brayne, C and De Silva, R and Wharton, SB (2007) Population variation in tau pathology in the aged hippocampus in the MRC-CFAS neuropathology cohort. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 263 - 263). BLACKWELL PUBLISHING |
| Lashley, T and Holton, JL and Gray, E and Kirkham, K and Dunn, L and Wood, N and Lees, AJ and Revesz, T (2007) A beta and alpha-synuclein pathologies in Parkinson's disease. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 256 - 256). BLACKWELL PUBLISHING |
| Laura, M and Houlden, H and Blake, J and Reilly, MM (2007) Autosomal dominant and recessive distal hereditary motor neuropathy caused by mutations in the heat shock protein 27. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. 49 - 49). BLACKWELL PUBLISHING |
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