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Number of items: 143.
A
| Abou-Sleiman, PM and Hanna, MG and Wood, NW (2006) Genetic association studies of complex neurological diseases. J NEUROL NEUROSUR PS , 77 (12) 1302 - 1304. 10.1136/jnnp.2005.082024. |
| Abou-Sleiman, PM and Muqit, MMK and McDonald, NQ and Yang, YX and Gandhi, S and Healy, DG and Harvey, K and Harvey, RJ and Deas, E and Hatia, K and Quinn, N and Lees, A and Latchman, DS and Wood, NW (2006) A heterozygous effect for PINK1 mutations in Parkinson's disease? ANN NEUROL , 60 (4) 414 - 419. 10.1002/ana.20960. |
| Abou-Sleiman, PM and Muqit, MMK and Wood, NW (2006) Expanding insights of mitochondrial dysfunction in Parkinson's disease. NAT REV NEUROSCI , 7 (3) 207 - 219. 10.1038/nrn1868. |
| Adighibe, O and Arepalli, S and Duckworth, J and Hardy, J and Wavrant-De Vrieze, F (2006) Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease. NEUROBIOLOGY OF AGING , 27 (10) 1431 - 1434. 10.1016/j.neurobiolaging.2005.08.010. |
B
| Bandopadhyay, R and Coulter, I and Kumaran, R and Lashley, T and Kingsbury, A and de Silva, R and Holton, J and Revesz, T and Lees, A (2006) DJ-1 (PARK-7) protein in neuronal and glial inclusions in neurodegenerative disorders. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 221 - 221). BLACKWELL PUBLISHING |
| Bandopadhyay, R and Kingsbury, AE and Harvey, K and de Silva, R and Lees, AJ (2006) Expression of LRRK2/dardarin and alpha-synuclein in Park8 mutated brains. In: MOVEMENT DISORDERS. (pp. S350 - S350). WILEY-LISS |
| Bender, A and Krishnan, KJ and Morris, CM and Taylor, GA and Reeve, AK and Perry, RH and Jaros, E and Hersheson, JS and Betts, J and Klopstock, T and Taylor, RW and Turnbull, DM (2006) High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease. NAT GENET , 38 (5) 515 - 517. 10.1038/ng1769. |
| Bettencourt, CB and et al., (2006) Polymorphism of the APOE locus in the Azores Islands (Portugal). Hum Biol , 78 (4) 509 - 512. 10.1353/hub.2006.0053. |
| Blazquez, L and Otaegui, D and Saenz, A and Paisan-Ruiz, C and Emparanza, JI and Ruiz-Martinez, J and Moreno, F and Marti-Masso, JF and de Munain, AL (2006) Apolipoprotein E epsilon 4 allele in familial and sporadic Parkinson's disease. NEUROSCI LETT , 406 (3) 235 - 239. 10.1016/j.neulet.2006.07.037. |
| Borhani Haghighi, A and Houlden, H and Lankarani, KB and Taghavi, A and Masnadi, K and Ashraf, AR and Safari, A (2006) A novel DNA sequence variation in the first genetically confirmed allgrove syndrome in iran. J Clin Neuromuscul Dis , 7 (3) 123 - 127. 10.1097/01.cnd.0000208261.93426.ab. |
| Bras, JM and Guerreiro, RJ and Morgadinho, AS and Januario, C and Oliveira, CR and Singleton, A (2006) Genes and Parkinson's disease - A clinic-based study in a Portuguese cohort. In: MOVEMENT DISORDERS. (pp. S53 - S53). WILEY-LISS |
C
| Cano, SJ and Hobart, JC and Edwards, M and Fitzpatrick, R and Bhatia, K and Thompson, AJ and Warner, TT (2006) CDIP-58 can measure the impact of botulinum toxin treatment in cervical dystonia. NEUROLOGY , 67 (12) 2230 - 2232. |
| Caswell, R and Warner, T and Mehta, A and Ginsberg, L (2006) POEMS syndrome. Practical Neurology , 6 (2) 111 - 116. |
| Caswell, R and Warner, TT and Mehta, A and Ginsberg, L (2006) POEMS syndrome. Practical Neurology , 6 14 - 26. |
| Chegounchi, M and Hanna, MG and Neild, GH (2006) Progressive neurological disease induced by tacrolimus in a renal transplant recipient: case presentation. BMC Nephrol , 7 7 - ?. 10.1186/1471-2369-7-7. |
| Chow, G and Beesley, CE and Robson, K and Winchester, BG and Holton, JL (2006) Case of X-linked myopathy with excessive autophagy. J CHILD NEUROL , 21 (5) 431 - 433. 10.2310/7010.2006.00117. |
| Clarimon, J and Scholz, S and Fung, HC and Hardy, J and Eerola, J and Hellstrom, O and Chen, CM and Wu, YR and Tienari, PJ and Singleton, A (2006) Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease. AMERICAN JOURNAL OF HUMAN GENETICS , 78 (6) 1082 - 1084. 10.1086/504727. |
| Cookson, MR and Hardy, J (2006) Clinical implications of basic research: The persistence of memory. NEW ENGLAND JOURNAL OF MEDICINE , 355 (25) 2697 - 2698. 10.1056/NEJMcibr065999. |
D
| de Silva, R and Lashley, T and Strand, C and Shiarli, AM and Shi, J and Tian, JZ and Bailey, KL and Davies, P and Bigio, EH and Arima, K and Iseki, E and Murayama, S and Kretzschmar, H and Neumann, M and Lippa, C and Halliday, G and MacKenzie, J and Ravid, R and Dickson, D and Wszolek, Z and Iwatsubo, T and Pickering-Brown, SM and Holton, J and Lees, A and Revesz, T and Mann, DMA (2006) An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R-and 4R-specific tau monoclonal antibodies. ACTA NEUROPATHOL , 111 (4) 329 - 340. 10.1007/s00401-006-0048-x. |
| de Silva, R and Lashley, T and Strand, K and Shiarli, AM and Revesz, T and Mann, DMA (2006) An immunohistochemical study of sporadic and inherited frontotemporal lobar degeneration using 3R-and 4R-specific monoclonal tau antibodies. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 235 - 235). BLACKWELL PUBLISHING |
| Djureinovic, T and Skoglund, J and Vandrovcova, J and Zhou, XL and Kalushkova, A and Iselius, L and Lindblom, A (2006) A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer. GUT , 55 (3) 362 - 366. 10.1136/gut.2005.075333. |
| Duenas, AM and Goold, R and Giunti, P (2006) Molecular pathogenesis of spinocerebellar ataxias. BRAIN , 129 1357 - 1370. |
E
| Edwards-Lee, T and Wen, J and Bell, J and Hardy, J and Chung, J and Momeni, P (2006) A presenilin-1 mutation (T245P) in transmembrane domain 6 causes early onset Alzheimer's disease. NEUROSCIENCE LETTERS , 398 (3) 251 - 252. 10.1016/j.neulet.2006.01.006. |
F
| Fidani, L and Kalinderi, K and Bostantjopoulou, S and Clarimon, J and Goulas, A and Katsarou, Z and Hardy, J and Kotsis, A (2006) Association of the Tau haplotype with Parkinson's disease in the Greek population. MOVEMENT DISORDERS , 21 (7) 1036 - 1039. 10.1002/mds.20864. |
| Fung, HC and Chen, CM and Hardy, J and Hernandez, D and Singleton, A and Wu, YR (2006) Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease. MOVEMENT DISORD , 21 (6) 880 - 881. 10.1002/mds.20814. |
| Fung, HC and Chen, CM and Hardy, J and Singleton, AB and Lee-Chen, GJ and Wu, YR (2006) Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan. NEUROSCI LETT , 394 (1) 33 - 36. 10.1016/j.neulet.2005.10.005. |
| Fung, HC and Chen, CM and Hardy, J and Singleton, AB and Wu, YR (2006) A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan. BMC Neurology , 6 , Article 47. 10.1186/1471-2377-6-47. |  |
| Fung, HC and Scholz, S and Matarin, M and Simon-Sanchez, J and Hernandez, D and Britton, A and Gibbs, JR and Langefeld, C and Stiegert, ML and Schymick, J and Okun, MS and Mandel, RJ and Fernandez, HH and Foote, KD and Rodriguez, RL and Peckham, E and De Vrieze, FW and Gwinn-Hardy, K and Hardy, JA and Singleton, A (2006) Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. LANCET NEUROL , 5 (11) 911 - 916. 10.1016/S1474-4422(06)70578-6. |
| Fung, HC and Xiromerisiou, G and Gibbs, JR and Wu, YR and Eerola, J and Gourbali, V and Hellstrom, O and Chen, CM and Duckworth, J and Papadimitriou, A and Tienari, PJ and Hadjigeorgiou, GM and Hardy, J and Singleton, AB (2006) Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohorts. NEURODEGENER DIS , 3 (6) 327 - 333. 10.1159/000097301. |
G
| Gandhi, S and Muqit, MMK and Abou-Sleiman, PM and Stanyer, L and Hargreaves, I and Heales, S and Ganguly, M and Latchman, DS and Holton, J and Wood, NW and Revesz, T (2006) PINK1: a novel mitochondrial protein in Parkinson's disease. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 221 - 222). BLACKWELL PUBLISHING |
| Gandhi, S and Muqit, MMK and Stanyer, L and Healy, DG and Abou-Sleiman, PM and Hargreaves, I and Heales, S and Ganguly, M and Parsons, L and Lees, AJ and Latchman, DS and Holton, JL and Wood, NW and Revesz, T (2006) PINK1 protein in normal human brain and Parkinson's disease. BRAIN , 129 1720 - 1731. 10.1093/brain/awl114. |
| Garcia, ML and Singleton, AB and Hernandez, D and Ward, CM and Evey, C and Sapp, PA and Hardy, J and Brown, RH and Cleveland, DW (2006) Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis. NEUROBIOLOGY OF DISEASE , 21 (1) 102 - 109. 10.1016/j.nbd.2005.06.016. |
| Geser, F and Wenning, GK and Seppi, K and Stampfer-Kountchev, M and Scherfler, C and Sawires, M and Frick, C and Ndayisaba, J-P and Ulmer, H and Pellecchia, MT and Barone, P and Kim, HT and Hooker, J and Quinn, NP and Cardozo, A and Tolosa, E and Abele, M and Klockgether, T and Østergaard, K and Dupont, E and Schimke, N and Eggert, KM and Oertel, W and Djaldetti, R and Poewe, W and Dodel, R and Tison, F and Ghorayeb, I and Pollak, P and Kölensperger, M and Diem, A and Deuschl, G and Daniels, C and Kopper, F and Sampaio, C and Coelho, M and Ferreira, J and Rosa, MM and Pirtosek, Z and Lees, AJ and Brooks, DJ and Fowler, C and Revesz, T and Gerhard, A and Holton, J and Schrag, A and Wood, N and Bozi, M and Scaravilli, T and Lindvall, O and Widner, H and Nilsson, CF and Grabowski, M and Krisp, A and Möller, C and Albanese, A and del Sorbo, F and Carella, F and Meco, G and Colosimo, C and Berciano, J and Gonzalez-Mandly, A and Giladi, N and Gurevich, T and Rascol, O and Galitzky, M and Ory, F and Gasser, T and Kamm, C and Buerk, K and Maass, S and Aquilonius, S-M and Bergquist, J (2006) Progression of multiple system atrophy (MSA): A prospective natural history study by the European MSA study group (EMSA SG). Movement Disorders , 21 (2) 179 - 186. |
| Ghiso, J and Rostagno, A and Tomidokoro, Y and Lashley, T and Bojsen-Moller, M and Braendgaard, H and Plant, G and Holton, J and Lal, R and Revesz, T and Frangione, B (2006) Genetic alterations of the BRI2 gene: Familial British and Danish dementias. BRAIN PATHOL , 16 (1) 71 - 79. |
| Giunti, P and Stephenson, DA and Johnson, J and Abu-sleiman, P and Davis, MB and Houlden, H and Worth, PF and Gardner-Thorpe, C and Wood, NW and EuroSca, (2006) Linkage analysis on the SCA11 locus. In: MOVEMENT DISORDERS. (pp. S336 - S336). WILEY-LISS |
| Graves, TD and Schorge, S and Davies, RA and Wood, NW and Kullmann, DM and Hanna, MG (2006) The role of the brain P/Q-type calcium channel in human epilepsy. EUR J NEUROL , 13 313 - 313. |
| Greenfield, J and Treacy, C and Giunti, P (2006) Centres of Excellence for the care of people with progressive ataxias. Br J Nurs , 15 (17) 932 - 936. |
| Greggio, E and Jain, S and Kingsbury, A and Bandopadhyay, R and Lewis, P and Kaganovich, A and van der Brug, MP and Beilina, A and Blackinton, J and Thomas, KJ and Ahmad, R and Miller, DW and Kesavapany, S and Singleton, A and Lees, A and Harvey, RJ and Harvey, K and Cookson, MR (2006) Kinase activity is required for the toxic effects of mutant LRRK2/dardarin. NEUROBIOL DIS , 23 (2) 329 - 341. 10.1016/j.nbd.2006.04.001. |
| Grupe, A and Li, YH and Rowland, C and Nowotny, P and Hinrichs, AL and Smemo, S and Kauwe, JSK and Maxwell, TJ and Cherny, S and Doil, L and Tacey, K and van Luchene, R and Myers, A and Vrieze, FW and Kaleem, M and Hollingworth, P and Jehu, L and Foy, C and Archer, N and Hamilton, G and Holmans, P and Morris, CM and Catanese, J and Sninsky, J and White, TJ and Powell, J and Hardy, J and O'Donovan, M and Lovestone, S and Jones, L and Morris, JC and Thal, L and Owen, M and Williams, J and Goate, A (2006) A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. AMERICAN JOURNAL OF HUMAN GENETICS , 78 (1) 78 - 88. 10.1086/498851. |
| Guerreiro, RJ and Bras, JM and Santana, I and Januario, C and Santiago, B and Morgadinho, AS and Ribeiro, MH and Hardy, J and Singleton, A and Oliveira, C (2006) Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort. BMC Neurology , 6 , Article 24. 10.1186/1471-2377-6-24. | |
H
| Hanna, MG (2006) Genetic neurological channelopathies. NAT CLIN PRACT NEURO , 2 (5) 252 - 263. 10.1038/ncpneuro0178. |
| Hardy, J (2006) A hundred years of Alzheimer's disease research. NEURON , 52 (1) 3 - 13. 10.1016/j.neuron.2006.09.016. |
| Hardy, J (2006) Amyloid double trouble. NATURE GENETICS , 38 (1) 11 - 12. 10.1038/ng0106-11. |
| Hardy, J (2006) Bad luck: An unappreciated limitation in the interpretation of twin studies. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 141B (6) 681 - 681. 10.1002/ajmg.b.30353. |
| Hardy, J (2006) No definitive evidence for a role for the environment in the etiology of Parkinson's disease. MOVEMENT DISORDERS , 21 (10) 1790 - 1791. 10.1002/mds.21067. |
| Hardy, J (2006) Progress in deciding a therapeutic approach to PSP. In: MOVEMENT DISORDERS. (pp. 437 - 438). WILEY-LISS |
| Hardy, J and Cai, H and Cookson, MR and Gwinn-Hardy, K and Singleton, A (2006) Genetics of Parkinson's disease and parkinsonism. ANNALS OF NEUROLOGY , 60 (4) 389 - 398. 10.1002/ana.21022. |
| Hardy, J and Cullen, K (2006) Amyloid at the blood vessel wall. NATURE MEDICINE , 12 (7) 756 - 757. 10.1038/nm0706-756. |
| Hardy, J and Momeni, P and Traynor, BJ (2006) Frontal temporal dementia: dissecting the aetiology and pathogenesis. BRAIN , 129 830 - 831. 10.1093/brain/awl035. |
| Hardy, J and Orr, H (2006) The genetics of neurodegenerative diseases. J NEUROCHEM , 97 (6) 1690 - 1699. 10.1111/j.1471-4159.2006.03979.x. |
| Hardy, J and Pittman, A and Myers, A and Fung, HC and de Silva, R and Duckworth, J (2006) Tangle diseases and the tau haplotypes. ALZ DIS ASSOC DIS , 20 (1) 60 - 62. |
| Hardy, J and Scholz, S and Evans, W and Goldfarb, L and Singleton, A (2006) Prion genotypes in Central America suggest selection for the V129 allele. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 141B (1) 33 - 35. 10.1002/ajmg.b.30248. |
| Healy, D and Muqit, M and Abu Sleiman, P and Yang, Y and Holton, J and Revesz, T and Quinn, N and Bhatia, K and Diss, J and Andrew, L and Latchmann, D and Wood, N (2006) A novel 5'UTR mutation of Nurr1 reduces Nurr1 expression in Parkinson's disease brain in vivo. In: MOVEMENT DISORDERS. (pp. S401 - S402). WILEY-LISS |
| Healy, DG and Abou-Sleiman, PM and Ahmadi, KR and Gandhi, S and Muqit, MM and Bhatia, KP and Quinn, NP and Lees, AJ and Holton, JL and Revesz, T and Wood, NW (2006) NR4A2 genetic variation in sporadic Parkinson's disease: A genewide approach. MOVEMENT DISORD , 21 (11) 1960 - 1963. 10.1002/mds.21018. |
| Healy, DG and Abou-Sleiman, PM and Casas, JP and Ahmadi, KR and Lynch, T and Gandhi, S and Muqit, MMK and Foltynie, T and Barker, R and Bhatia, KP and Quinn, NP and Lees, AJ and Gibson, JM and Holton, JL and Revesz, T and Goldstein, DB and Wood, NW (2006) UCHL-1 is not a Parkinson's disease susceptibility gene. ANN NEUROL , 59 (4) 627 - 633. 10.1002/ana.20757. |
| Henley, SMD and Frost, C and MacManus, DG and Warner, TT and Fox, NC and Tabrizi, SJ (2006) Increased rate of whole-brain atrophy over 6 months in early Huntington disease. NEUROLOGY , 67 (4) 694 - 696. |
| Hodgetts, A (2006) SELDI-MS could diagnose TB and save children's lives. TRAC-TREND ANAL CHEM , 25 (9) III - III. 10.1016/j.trac.2006.08.002. |
| Holton, JL and Beesley, C and Jackson, M and Venner, K and Bhardwaj, N and Winchester, B and Al-Memar, A (2006) Autophagic vacuolar myopathy in twin girls. NEUROPATH APPL NEURO , 32 (3) 253 - 259. |
| Horvath, R and Hudson, G and Ferrari, G and Futterer, N and Ahola, S and Lamantea, E and Prokisch, H and Lochmuller, H and McFarland, R and Ramesh, V and Klopstock, T and Freisinger, P and Salvi, F and Mayr, JA and Santer, R and Tesarova, M and Zeman, J and Udd, B and Taylor, RW and Turnbull, D and Hanna, M and Fialho, D and Suomalainen, A and Zeviani, M and Chinnery, PF (2006) Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. BRAIN , 129 1674 - 1684. 10.1093/brain/awl088. |
| Houlden, H and Edwards, M and McNeil, J and Greenwood, R (2006) Use of the Barthel Index and the Functional Independence Measure during early inpatient rehabilitation after single incident brain injury. CLIN REHABIL , 20 (2) 153 - 159. 10.1191/0269215506cr917oa. |
| Houlden, H and Greenwood, R (2006) Apolipoprotein E4 and traumatic brain injury. J NEUROL NEUROSUR PS , 77 (10) 1106 - 1107. 10.1136/jnnp.2006.095513. |
| Houlden, H and King, R and Blake, J and Groves, M and Love, S and Woodward, C and Hammans, S and Nicoll, J and Lennox, G and O'Donovan, DG and Gabriel, C and Thomas, PK and Reilly, MM (2006) Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I). BRAIN , 129 411 - 425. 10.1093/brain/awh712. |
| Houlden, H and Reilly, MM (2006) Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease. NEUROMOL MED , 8 (1-2) 43 - 62. 10.1385/NMM:8:1-2:43. |
| Houlden, H and Reilly, MM (2006) Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease. Neuromolecular Med , 8 (1-2) 43 - 62. 10.1385/NMM:8:1:243. |
| Hu, MTM and Scherfle, C and Khan, NL and Hajnal, JV and Lees, AJ and Quinn, N and Wood, NW and Brooks, DJ (2006) Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and Parkin-linked Parkinson's disease. MOVEMENT DISORD , 21 (3) 299 - 305. 10.1002/mds.20702. |
| Hudson, G and Deschauer, M and Taylor, RW and Hanna, MG and Fialho, D and Schaefer, AM and He, LP and Blakely, E and Turnbull, DM and Chinnery, PF (2006) POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions. NEUROLOGY , 66 (9) 1439 - 1441. |
| Huey, ED and Grafman, J and Wassermann, EM and Pietrini, P and Tierney, MC and Ghetti, B and Spina, S and Baker, M and Hutton, M and Elder, JW and Berger, SL and Heflin, KA and Hardy, J and Momeni, P (2006) Characteristics of frontotemporal dementia patients with a progranulin mutation. ANNALS OF NEUROLOGY , 60 (3) 374 - 380. 10.1002/ana.20969. |
I
| Ingelsson, M and Ramasamy, K and Cantuti-Castelvetri, I and Skoglund, L and Matsui, T and Orne, J and Kowa, H and Raju, S and Vanderburg, CR and Augustinack, JC and de Silva, R and Lees, AJ and Lannfelt, L and Growdon, JH and Frosch, MP and Standaert, DG and Irizarry, MC and Hyman, BT (2006) No alteration in tau exon 10 alternative splicing in tangle-bearing neurons of the Alzheimer's disease brain. ACTA NEUROPATHOL , 112 (4) 439 - 449. 10.1007/s00401-006-0095-3. |
| Iseki, E and Yamamoto, R and Murayama, N and Minegishi, M and Togo, T and Katsuse, O and Kosaka, K and Akiyama, H and Tsuchiya, K and de Silva, R and Andrew, L and Arai, H (2006) Immunohistochemical investigation of neurofibrillary tangles and their tau isoforms in brains of limbic neurofibrillary tangle dementia. Neurosci Lett , 405 (1-2) 29 - 33. 10.1016/j.neulet.2006.06.036. |
J
| Jackson, TL and Hussain, A and Hodgetts, A and Morley, AMS and Hillenkamp, J and Sullivan, PM and Marshall, J (2006) Human scleral hydraulic conductivity: Age-related changes, topographical variation, and potential scleral outflow facility. INVEST OPHTH VIS SCI , 47 (11) 4942 - 4946. 10.1167/iovs.06-0362. |
| Jacques, TS and Eldridge, C and Patel, A and Saleem, NM and Powell, M and Kitchen, ND and Thom, M and Revesz, T (2006) Mixed glioneuronal tumour of the fourth ventricle with prominent rosette formation. NEUROPATH APPL NEURO , 32 (2) 217 - 220. 10.1111/j.1365-2990.2005.00692.x. |
K
| Kidd, DP and Revesz, T and Miller, NR (2006) Rosai-Dorfman disease presenting with widespread intracranial and spinal cord involvement. NEUROLOGY , 67 (9) 1551 - 1555. |
| Kinghorn, KJ and Crowther, DC and Sharp, LK and Nerelius, C and Davis, RL and Chang, HT and Green, C and Gubb, DC and Johansson, J and Lomas, DA (2006) Neuroserpin binds Abeta and is a neuroprotective component of amyloid plaques in Alzheimer disease. J Biol Chem , 281 (39) 29268 - 29277. 10.1074/jbc.M600690200. |
| Kingsbury, A and Bandopadhyay, R and Lees, A (2006) DJ-1 (PARK7) mRNA expression in human brain. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 234 - 234). BLACKWELL PUBLISHING |
| Kinirons, P and Cavalleri, GL and Shahwan, A and Wood, NW and Goldstein, DB and Sisodiya, SM and Delanty, N and Doherty, CP (2006) Examining the role of common genetic variation in the gamma 2 subunit of the GABA(A) receptor in epilepsy using tagging SNPs. EPILEPSY RES , 70 (2-3) 229 - 238. 10.1016/j.eplepsyres.2005.05.009. |
| Kinirons, P and Cavalleri, GL and Shahwan, A and Wood, NW and Goldstein, DB and Sisodiya, SM and Delanty, N and Doherty, CP (2006) Examining the role of common genetic variation in the gamma2 subunit of the GABA(A) receptor in epilepsy using tagging SNPs. Epilepsy Res , 70 (2-3) 229 - 238. 10.1016/j.eplepsyres.2006.05.009. |
| Kinirons, P and Cavalleri, GL and Singh, R and Shahwan, A and Acheson, JF and Wood, NW and Goldstein, DB and Sisodiya, SM and Doherty, CP and Delanty, N (2006) A pharmacogenetic exploration of vigabatrin-induced visual field constriction. EPILEPSY RES , 70 (2-3) 144 - 152. 10.1016/j.eplepsyres.2006.03.012. |
| Kohoutová, M and Stekrová, J and Sulová, M and Zidková, K and Kleibl, Z and Vandrovcová, J and Kebrdlová, V and Kotlas, J and Jirásek, V (2006) [Hereditary forms of colorectal adenomatous polyposis]. Cas Lek Cesk , 145 (6) 475 - 479. |
| Kumaran, R and Bandopadhyay, R and Lees, AJ (2006) Biochemical properties of DJ-1 (PARK 7) in human brain tissue. In: MOVEMENT DISORDERS. (pp. S347 - S348). WILEY-LISS |
L
| Lashley, T and Holton, JL and Verbeek, MM and Rostagno, A and Bojsen-Moller, M and David, G and van Horssen, J and Braendgaard, H and Plant, G and Frangione, B and Ghiso, J and Revesz, T (2006) Molecular chaperons, amyloid and preamyloid lesions in the BRI2 gene-related dementias: a morphological study. NEUROPATH APPL NEURO , 32 (5) 492 - 504. 10.1111/j.1365-2990.2006.00747.x. |
| Lewis, PA and Properzi, F and Prodromidou, K and Clarke, AR and Collinge, J and Jackson, GS (2006) Removal of the glycosylphosphatidylinositol anchor from PrPSc by cathepsin D does not reduce prion infectivity. BIOCHEM J , 395 443 - 448. 10.1042/BJ20051677. |
| Lewis, PA and Tattum, MH and Jones, S and Bhelt, D and Batchelor, M and Clarke, AR and Collinge, J and Jackson, GS (2006) Codon 129 polymorphism of the human prion protein influences the kinetics of amyloid formation. J GEN VIROL , 87 2443 - 2449. 10.1099/vir.0.81630-0. |
| Li, Y and Grupe, A and Rowland, C and Nowotny, P and Kauwe, JSK and Smemo, S and Hinrichs, A and Tacey, K and Toombs, TA and Kwok, S and Catanese, J and White, TJ and Maxwell, TJ and Hollingworth, P and Abraham, R and Rubinsztein, DC and Brayne, C and Wavrant-De Vrieze, F and Hardy, J and O'Donovan, M and Lovestone, S and Morris, JC and Thal, LJ and Owen, M and Williams, J and Goate, A (2006) DAPK1 variants are associated with Alzheimer's disease and allele-specific expression. HUMAN MOLECULAR GENETICS , 15 (17) 2560 - 2568. 10.1093/hmg/ddl178. |
| Lima, M and Santos, C and Bettencourt, C and Maciel, P (2006) Genetic testing for late-onset disorders: the experience of Machado-Joseph disease in the Azores Islands. In: Trends in Birth Defects Research. (83 - 94). Nova Publishers: New York. |
| Luk, CY and Giovannoni, G and Lees, AJ and de Silva, R (2006) Development of an ELISA for sensitive quantification of three-repeat and four-repeat tau isoforms in tauopathies and characterisation of tau isoforms in CSF. In: MOVEMENT DISORDERS. (pp. S345 - S345). WILEY-LISS |
| Lymperopoulos, K and Noad, R and Tosi, S and Nethisinghe, S and Brierley, I and Roy, P (2006) Specific binding of Bluetongue virus NS2 to different viral plus-strand RNAs. VIROLOGY , 353 (1) 17 - 26. 10.1016/j.virol.2006.04.022. |
M
| Malkani, R and D'Souza, I and Gwinn-Hardy, K and Scheenberg, GD and Hardya, J and Momeni, P (2006) A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia. NEUROBIOLOGY OF DISEASE , 22 (2) 401 - 403. 10.1016/j.nbd.2005.12.001. |
| Marchionni, I and Paffi, A and Pellegrino, M and Liberti, M and Apollonio, F and Abeti, R and Fontana, F and D'Inzeo, G and Mazzanti, M (2006) Comparison between low-level 50 Hz and 900 MHz electromagnetic stimulation on single channel ionic currents and on firing frequency in dorsal root ganglion isolated neurons. Biochim Biophys Acta , 1758 (5) 597 - 605. 10.1016/j.bbamem.2006.03.014. |
| Marlowe, L and Peila, R and Benke, KS and Hardy, J and White, LR and Launer, LJ and Myers, A (2006) Insulin-degrading enzyme haplotypes affect insulin levels but not dementia risk. NEURODEGENERATIVE DISEASES , 3 (6) 320 - 326. 10.1159/000097300. |
| Masellis, M and Momeni, P and Meschino, W and Jr, HR and Elder, J and Sato, C and Liang, Y and St George-Hyslop, P and Hardy, J and Bilbao, J and Black, S and Rogaeva, E (2006) Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome. BRAIN , 129 3115 - 3123. 10.1093/brain/awl276. |
| Matarin, MM and Singleton, AB and Houlden, H (2006) PANK2 gene analysis confirms genetic heterogeneity in neurodegeneration with brain iron accumulation (NBIA) but mutations are rare in other types of adult neurodegenerative disease. NEUROSCI LETT , 407 (2) 162 - 165. 10.1016/j.neulet.2006.08.030. |
| Merikangas, KR and Low, NCP and Hardy, J (2006) Commentary: Understanding sources of complexity in chronic diseases - the importance of integration of genetics and epidemiology. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY , 35 (3) 590 - 592. 10.1093/ije/dyl007. |
| Momeni, P and Bell, J and Duckworth, J and Hutton, M and Mann, D and Brown, SP and Hardy, J (2006) Sequence analysis of all identified open reading frames on the frontal temporal dementia haplotype on chromosome 3 fails to identify unique coding variants except in CHMP2B. NEUROSCIENCE LETTERS , 410 (2) 77 - 79. 10.1016/j.neulet.2006.06.065. |
| Momeni, P and Rogaeva, E and Van Deerlin, V and Yuan, W and Grafman, J and Tierney, M and Huey, E and Bell, J and Morris, CM and Kalaria, RN and van Rensburg, SJ and Niehaus, D and Potocnik, F and Kawarai, T and Salehi-Rad, S and Sato, C and George-Hyslop, PS and Hardy, J (2006) Genetic variability in CHMP2B and frontotemporal dementia. NEURODEGENERATIVE DISEASES , 3 (3) 129 - 133. 10.1159/000094771. |
| Momeni, P and Schymick, J and Jain, S and Cookson, MR and Cairns, NJ and Greggio, E and Greenway, MJ and Berger, S and Pickering-Brown, S and Chio, A and Fung, HC and Holtzman, DM and Huey, ED and Wassermann, EM and Adamson, J and Hutton, ML and Rogaeva, E and St George-Hyslop, P and Rothstein, JD and Hardiman, O and Grafman, J and Singleton, A and Hardy, J and Traynor, BJ (2006) Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD. BMC NEUROLOGY , 6 , Article ARTN 44. 10.1186/1471-2377-6-44. |
| Muqit, MM and Gandhi, S and Deas, E and Abou-Sleiman, PM and Harvey, K and Harvey, RJ and Wood, NW and Latchman, DS (2006) A site-directed mutagenesis study of putative cleavage sites of the Parkinson's disease associated gene, PINK1. In: MOVEMENT DISORDERS. (pp. S560 - S560). WILEY-LISS |
| Muqit, MMK and Abou-Sleiman, PM and Saurin, AT and Harvey, K and Gandhi, S and Deas, E and Eaton, S and Smith, MDP and Venner, K and Matilla, A and Healy, DG and Gilks, WP and Lees, AJ and Holton, J and Revesz, T and Parker, PJ and Harvey, RJ and Wood, NW and Latchman, DS (2006) Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress. J NEUROCHEM , 98 (1) 156 - 169. 10.1111/j.1471-4159.2006.03845.x. |
| Muqit, MMK and Gandhi, S and Wood, NW (2006) Mitochondria in Parkinson disease - Back in fashion with a little help from genetics. ARCH NEUROL-CHICAGO , 63 (5) 649 - 654. |
| Murphy, S and McNamara, B (2006) How well is peripheral neuropathy investigated? An audit from a regional neurophysiology department. Irish Journal of Medical Science , 175 (1) 54 - 56. |
N
| Nirmalananthan, N and Hanna, MG (2006) Predicting steroid response in muscle disease. J NEUROL NEUROSUR PS , 77 (10) 1104 - 1105. 10.1136/jnnp.2006.087874. |
O
| Ozawa, T and Healy, DG and Abou-Sleiman, PM and Ahmadi, KR and Quinn, N and Lees, AJ and Shaw, K and Wullner, U and Berciano, J and Moller, JC and Kamm, C and Burk, K and Josephs, KA and Barone, P and Tolosa, E and Goldstein, DB and Wenning, G and Geser, F and Holton, JL and Gasser, T and Revesz, T and Wood, NW and European MSA Study Group, (2006) The alpha-synuclein gene in multiple system atrophy. J NEUROL NEUROSUR PS , 77 (4) 464 - 467. 10.1136/jnnp.2005.073528. |
| Ozawa, T and Healy, DG and Quinn, NP and Bozi, M and Paviour, D and Josephs, KA and Lees, AJ and Wood, NW and Holton, JL and Revesz, T (2006) Clinicopathological features of patients with multiple system atrophy with a family history of Parkinson's disease. In: MOVEMENT DISORDERS. (pp. S527 - S527). WILEY-LISS |
P
| Paisan-Ruiz, C and Evans, EW and Jain, S and Xiromerisiou, G and Gibbs, JR and Eerola, J and Gourbali, V and Hellstrom, O and Duckworth, J and Papadimitriou, A and Tienari, PJ and Hadjigeorgiou, GM and Singleton, AB (2006) Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium. J MED GENET , 43 (2) , Article e9. 10.1136/jmg.2005.036889. |
| Parton, A and Malhotra, P and Nachev, P and Ames, D and Ball, J and Chataway, J and Husain, M (2006) Space re-exploration in hemispatial neglect. NEUROREPORT , 17 (8) 833 - 836. |
| Pittman, A and Myers, A and Hardy, J and Wood, N and Lees, AJ and de Silva, R (2006) Increased MAPT expression as the possible functional basis of the genetic association with PSP. In: MOVEMENT DISORDERS. (pp. S415 - S415). WILEY-LISS |
| Pittman, AM and Fung, HC and de Silva, R (2006) Untangling the tau gene association with neurodegenerative disorders. HUM MOL GENET , 15 R188 - R195. 10.1093/hmg/ddl190. |
R
| Revesz, T and Ghiso, J and Plant, GT and Lashley, T and Rostagno, A and Frangione, B and Holton, JL (2006) Cerebral Amyloid Angiopathy. In: Kalimo, H, (ed.) Cerebrovascular Diseases. (94 - 102). Wiley-Blackwell |
| Revesz, T and Holton, J (2006) Lewy body formation and deposition of amyloid-beta: Overlapping or synergistic pathologies? In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. 309 - 309). ELSEVIER SCIENCE BV |
S
| Schmitt, I and Wullner, U and Healy, DG and Wood, NW and Kolsch, H and Henn, R (2006) The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany. MOVEMENT DISORD , 21 (11) 2034 - 2034. 10.1002/mds.21082. |
| Schmitz-Hubsch, T and du Montcel, ST and Baliko, L and Berciano, J and Boesch, S and Depondt, C and Giunti, P and Globas, C and Infante, J and Kang, JS and Kremer, B and Mariotti, C and Melegh, B and Pandolfo, M and Rakowicz, M and Ribai, P and Rola, R and Schols, L and Szymanski, S and de Warrenburg, BPV and Durr, A and Klockgether, T (2006) Scale for the assessment and rating of ataxia - Development of a new clinical scale. NEUROLOGY , 66 (11) 1717 - 1720. 10.1212/01.wnl.0000219042.60538.92. |
| Schmitz-Hubsch, T and du Montcel, ST and Baliko, L and Boesch, S and Bonato, S and Fancellu, R and Giunti, P and Globas, C and Kang, JS and Kremer, B and Mariotti, C and Melegh, B and Rakowicz, M and Rola, R and Romano, S and Schols, L and Szymanski, S and van de Warrenburg, BPC and Zdzienicka, E and Durr, A and Klockgether, T (2006) Reliability and validity of the International Cooperative Ataxia Rating Scale: A study in 156 spinocerebellar ataxia patients. MOVEMENT DISORD , 21 (5) 699 - 704. 10.1002/mds.20781. |
| Schneider, SA and Mohire, MD and Trender-Gerhard, I and Asmus, F and Sweeney, M and Davis, M and Gasser, T and Wood, NW and Bhatia, KP (2006) Familial dopa-responsive cervical dystonia. NEUROLOGY , 66 (4) 599 - 601. |
| Schneider, SA and van de Warrenburg, BPC and Hughes, TD and Davis, M and Sweeney, M and Wood, N and Quinn, NP and Bhatia, KP (2006) Phenotypic homogeneity of the Huntington disease - like presentation in a SCA17 family. NEUROLOGY , 67 (9) 1701 - 1703. |
| Schott, JM and Williams, DR and Butterworth, R and Janssen, JC and Larner, AJ and Holton, JL and Rossor, MN (2006) Shunt responsive progressive supranuclear palsy. In: MOVEMENT DISORDERS. (pp. S524 - S524). WILEY-LISS |
| Schrag, A and Geser, F and StampferKountchev, M and Seppi, K and Sawires, M and Köllensperger, M and Scherfler, C and Quinn, N and Pellecchia, MT and Barone, P and del Sorbo, F and Albanese, A and Ostegaard, K and Dupont, E and Cardozo, A and Tolosa, E and Nilsson, CF and Widner, H and Lindvall, O and Giladi, N and Gurevich, T and Daniels, C and Deuschl, G and Coelho, M and Sampaio, C and Abele, M and Klockgether, T and Schimke, N and Eggert, KM and Oetel, W and Djaldetti, R and Colosimo, C and Meco, G and Poewe, W and Wenning, GK and Dodel, R and Tison, F and Ghorayeb, I and Yekhlef, F and Pollak, P and Stampfer-Kountchev, M and Diem, A and Ndayisaba, J-P and Kopper, F and Sampiao, C and Ferreira, J and Rosa, MM and Pirtosek, Z and Quinn, NP and Lees, AJ and Mathias, CJ and Brooks, DJ and Fowler, C and Revesz, T and Gerhard, A and Holton, J and Wood, N and Grabowski, M and Oertel, W and Carella, F and Barciano, J and Gonzalez-Mandly, A and Guverich, T and Rascol, O and Galitzky, M and Ory, F and Gasser, T and Kamm, C and Buerk, K and Maass, S and Aquilonius, S-M and Berquist, J (2006) Health-related quality of life in multiple system atrophy. Movement Disorders , 21 (6) 809 - 815. |
| Schrag, A. and Selai, C. and Quinn, N. and Lees, A. and Litvan, I. and Lang, A. and Poon, Y. and Bower, J. and Burn, D. and Hobart, J. (2006) Measuring quality of life in PSP: the PSP-QoL. Neurology , 67 (1) pp. 39-44. 10.1212/01.wnl.0000223826.84080.97. |
| Seal, JL and Gornick, MC and Gogtay, N and Shaw, P and Greenstein, DK and Coffey, M and Gochman, PA and Stromberg, T and Chen, Z and Merriman, B and Nelson, SF and Brooks, J and Arepalli, S and Wavrant-De Vrieze, F and Hardy, J and Rapoport, JL and Addington, AM (2006) Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia. JOURNAL OF MEDICAL GENETICS , 43 (11) 887 - 892. 10.1136/jmg.2006.043380. |
| Sharma, M and Mueller, JC and Zimprich, A and Lichtner, P and Hofer, A and Leitner, P and Maass, S and Berg, D and Durr, A and Bonifati, V and De Michele, G and Oostra, B and Brice, A and Wood, NW and Muller-Myhsok, B and Gasser, T and European Consortium Genetic Suscep, (2006) The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations. J MED GENET , 43 (7) 557 - 562. 10.1136/jmg.2005.039149. |
| Sharp, LK and Mallya, M and Kinghorn, KJ and Wang, Z and Crowther, DC and Huntington, JA and Belorgey, D and Lomas, DA (2006) Sugar and alcohol molecules provide a therapeutic strategy for the serpinopathies that cause dementia and cirrhosis. FEBS J , 273 (11) 2540 - 2552. 10.1111/j.1742-4658.2006.05262.x. |
| Shatunov, A and Sambuughin, N and Jankovic, J and Elble, R and Lee, HS and Singleton, AB and Dagvadorj, A and Ji, J and Zhang, Y and Kimonis, VE and Hardy, J and Hallett, M and Goldfarb, LG (2006) Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23. BRAIN , 129 2318 - 2331. 10.1093/brain/awl120. |
| Shaw-Smith, C and Pittman, A and Willatt, L and Martin, H and Rickman, L and Gribble, S and Rosenberg, C and Firth, HV and de Silva, R and Carter, NP (2006) Microdeletion encompassing the MAPT gene at chromosome 17q21.3 is associated with developmental delay and learning disability. In: JOURNAL OF MEDICAL GENETICS. (pp. S52 - S52). B M J PUBLISHING GROUP |
| Shaw-Smith, C and Pittman, AM and Willatt, L and Martin, H and Rickman, L and Gribble, S and Curley, R and Cumming, S and Dunn, C and Kalaitzopoulos, D and Porter, K and Prigmore, E and Krepischi-Santos, AC and Varela, MC and Koiffmann, CP and Lees, AJ and Rosenberg, C and Firth, HV and de Silva, R and Carter, NP (2006) Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nat Genet , 38 (9) 1032 - 1037. 10.1038/ng1858. |
| Shaw-Smith, C and Pittman, AM and Willatt, L and Martin, H and Rickman, L and Gribble, S and Curley, R and Cumming, S and Dunn, C and Kalaitzopoulos, D and Porter, K and Prigmore, E and Krepischi-Santos, ACV and Varela, MC and Koiffmann, CP and Lees, AJ and Rosenberg, C and Firth, HV and de Silva, R and Carter, NP (2006) Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. NAT GENET , 38 (9) 1032 - 1037. 10.1038/ng1864. |
| Shaw-Smith, C and Pittman, AM and Willatt, L and Martin, H and Rickman, L and Gribble, S and Curley, R and Cumming, S and Dunn, C and Kalaitzopoulos, D and Porter, K and Prigmore, E and Krepischi-Santos, ACV and Varela, MC and Koiffmann, CP and Lees, AJ and Rosenberg, C and Firth, HV and De Silva, R and Carter, NP (2006) Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nature Genetics , 38 (9) 1032 - 1037. |
| Shaw-Smith, C. and Pittman, A.M. and Willatt, L. and Martin, H. and Rickman, L. and Gribble, S. and Curley, R. and Cumming, S. and Dunn, C. and Kalaitzopoulos, D. and Porter, K. and Prigmore, E. and Krepischi-Santos, A.C.V. and Varela, M.C. and Koiffmann, C.P. and Lees, A.J. and Rosenberg, C. and Firth, H.V. and de Silva, R. and Carter, N.P. (2006) Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nature Genetics , 38 (9) pp. 1032-1037. 10.1038/ng1858. |
| Silveira-Moriyama, L and Bandopadhyay, R and Kingsbury, AE and Lees, AJ (2006) DJ-1 (PARK 7) immunoreactivity in the anterior olfactory nucleus and olfactory tract of Parkinson's disease, progressive supranuclear palsy and control cases. In: MOVEMENT DISORDERS. (pp. S343 - S343). WILEY-LISS |
| Simon-Sanchez, J and Marti-Masso, JF and Sanchez-Mut, JV and Paisan-Ruiz, C and Martinez-Gil, A and Ruiz-Martinez, J and Saenz, A and Singleton, AB and de Munain, AL and Perez-Tur, J (2006) Parkinson's disease due to the R1441G mutation in Dardarin: A founder effect in the Basques. MOVEMENT DISORD , 21 (11) 1954 - 1959. 10.1002/mds.21114. |
| Skoglund, J and Djureinovic, T and Zhou, XL and Vandrovcova, J and Renkonen, E and Iselius, L and Bisgaard, ML and Peltomaki, P and Lindblom, A (2006) Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32-31.1. J MED GENET , 43 (2) ? - ?. 10.1136/jmg.2005.033928. |
| Smemo, S and Nowotny, P and Hinrichs, AL and Kauwe, JSK and Cherny, S and Erickson, K and Myers, AJ and Kaleem, M and Marlowe, L and Gibson, AM and Hollingworth, P and O'Donovan, MC and Morris, CM and Holmans, P and Lovestone, S and Morris, JC and Thal, L and Li, YH and Grupe, A and Hardy, J and Owen, MJ and Williams, J and Goate, A (2006) Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. ANNALS OF NEUROLOGY , 59 (1) 21 - 26. 10.1002/ana.20673. |
| Stanyer, L and Jorgensen, W and Clark, JB and Heales, SJ (2006) Oxidative inactivation of mitochondrial ion protease precedes electron transport chain (ETC) dysfunction. In: JOURNAL OF NEUROCHEMISTRY. (pp. 50 - 50). BLACKWELL PUBLISHING |
| Strand, C and Williams, D and De Silva, R and Holton, J and Revesz, T (2006) Determining 3-repeat tau pathology in PSP. In: MOVEMENT DISORDERS. (pp. S525 - S525). WILEY-LISS |
U
| Ule, J and Darnell, RB (2006) RNA binding proteins and the regulation of neuronal synaptic plasticity. Curr Opin Neurobiol , 16 102 - 110. |
| Ule, J and Stefani, G and Mele, A and Ruggiu, M and Wang, X and Taneri, B and Gaasterland, T and Blencowe, BJ and Darnell, RB (2006) An RNA map predicting Nova-dependent splicing regulation. Nature , 444 580 - 586. |
V
| Valente, E and Brady, JD and McGregor, L and Soutar, M and Vazquez, M and Wilson, L (2006) Performance evaluation of an automated microparticle enzyme immunoassay (MEIA) for holo-transcobalamin, AxSYM (R) HoloTC. In: CLINICAL CHEMISTRY. (pp. A179 - A179). AMER ASSOC CLINICAL CHEMISTRY |
| van de Warrenburg, BP and Giunti, P and Schneider, SA and Quinn, NP and Wood, NW and Bhatia, KP (2006) The syndrome of (predominantly cervical) dystonia and cerebellar ataxia: new cases indicate a distinct but heterogeneous entity. In: MOVEMENT DISORDERS. (pp. S338 - S339). WILEY-LISS |
| Vandrovcova, J and Lagerstedt-Robinsson, K and Pahlman, L and Lindblom, A (2006) Somatic BRAF-V600E mutations in familial colorectal cancer. CANCER EPIDEM BIOMAR , 15 (11) 2270 - 2273. 10.1158/1055-9965.EPI-06-0359. |
| Varsani, H and Newton, KR and Li, CK and Holton, JL and Harding, B and Wedderburn, LR (2006) Quantitative analysis of paediatric muscle biopsies reported as 'normal': Establishing a comparator cohort. In: ANNALS OF THE RHEUMATIC DISEASES. (pp. 574 - 574). B M J PUBLISHING GROUP |
| Venance, SL and Cannon, SC and Fialho, D and Fontaine, B and Hanna, MG and Ptacek, LJ and Tristani-Firouzi, M and Tawil, R and Griggs, RC and CINCH investigators, (2006) The primary periodic paralyses: diagnosis, pathogenesis and treatment. BRAIN , 129 8 - 17. 10.1093/brain/awh639. |
W
| Wedderburn, LR and Varsani, H and Li, CK and Amato, AA and Banwell, B and Bove, KE and Corse, AM and Emslie-Smith, A and Harding, B and Hoogendijk, J and Lundberg, IE and Marie, SK and Minetti, C and Nennesmo, I and Rushing, EJ and Sewry, C and Newton, KR and Allen, E and Charman, SC and Pilkington, CA and Holton, J (2006) A proposed score tool with which to define abnormalities on muscle biopsy from children with juvenile dermatomyositis. In: ARTHRITIS AND RHEUMATISM. (pp. S657 - S658). WILEY-LISS |
| Williams, DR and Revesz, T and Lees, AJ (2006) Pure akinesia with gait freezing: A 3rd PSP phenotype. In: MOVEMENT DISORDERS. (pp. S537 - S537). WILEY-LISS |
| Wood, NW (2006) Pharmacogenetic approaches to neurological disease - Epilepsy as an example. EUR J NEUROL , 13 1 - 1. |
| Wood-Kaczmar, A and Gandhi, S and Wood, NW (2006) Understanding the molecular causes of Parkinson's disease. TRENDS MOL MED , 12 (11) 521 - 528. 10.1016/j.molmed.2006.09.007. |
Y
| Yokota, O and Tsuchiya, K and Oda, T and Ishihara, T and de Silva, R and Lees, AJ and Arai, T and Uchihara, T and Ishizu, H and Kuroda, S and Akiyama, H (2006) Amyotrophic lateral sclerosis with dementia: an autopsy case showing many Bunina bodies, tau-positive neuronal and astrocytic plaque-like pathologies, and pallido-nigral degeneration. ACTA NEUROPATHOL , 112 (5) 633 - 645. 10.1007/s00401-006-0141-1. |