- Detailed search
-
- Browse by:
- Department |
Year |
Latest
For everyone
- About UCL Discovery
- Open Access
- Using UCL Discovery:
- Statistics:
- FAQ
For UCL authors
Browse by UCL Departments and Centres
 | Up a level |
Group by: Author | Type
Number of items: 114.
A
| Abou-Sleiman, PM and Healy, DG and Ahmadi, K and Goldstein, DB and Wood, NW (2003) Population genetic approaches to Parkinsons disease. In: AMERICAN JOURNAL OF HUMAN GENETICS. (pp. 541 - 541). UNIV CHICAGO PRESS |
| Abou-Sleiman, PM and Healy, DG and Quinn, N and Lees, AJ and Wood, NW (2003) The role of pathogenic DJ-1 mutations in Parkinson's disease. ANN NEUROL , 54 (3) 283 - 286. 10.1002/ana.10675. |
| Abramov, A.Y. and Canevari, L. and Duchen, M.R. (2003) Changes in intracellular calcium and glutathione in astrocytes as the primary mechanism of amyloid neurotoxicity. Nature Chemical Biology , 23 (12) pp. 5088-5095. |  |
| Abramov, AY and Canevari, L and Duchen, MR (2003) Amyloid beta peptide causes [Ca2+](c) fluctuations and decreases [GSH] in rat astrocytes. In: BIOPHYSICAL JOURNAL. (pp. 389A - 389A). BIOPHYSICAL SOCIETY |
| Abramov, AY and Canevari, L and Duchen, MR (2003) Changes in intracellular calcium and glutathione in astrocytes as the primary mechanism of amyloid neurotoxicity. J NEUROSCI , 23 (12) 5088 - 5095. |
| Abramov, AY and Duchen, MR (2003) Actions of ionomycin, 4-BrA23187 and a novel electrogenic Ca2+ ionophore on mitochondria in intact cells. CELL CALCIUM , 33 (2) 101 - 112. |
| Ahmad-Annuar, A and Shah, P and Hafezparast, M and Hummerich, H and Witherden, AS and Morrison, KE and Shaw, PJ and Kirby, J and Warner, TT and Crosby, A and Proukakis, C and Wilkinson, P and Orrell, RW and Bradley, L and Martin, JE and Fisher, EMC (2003) No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders. AMYOTROPH LATERAL SC , 4 (3) 150 - 157. |
| Alves, JD and Ames, PRJ and Donohue, S and Stanyer, L and Nourooz-Zadeh, J and Ravirajan, C and Isenberg, DA (2003) Antibodies to high-density lipoprotein and beta(2)-glycoprotein I are inversely correlated with paraoxonase activity in systematic lupus erythematosus (vol 46, pg 2686, 2002). ARTHRITIS RHEUM , 48 (1) 284 - 284. 10.1002/art.539. |
| Andorfer, C and Kress, Y and Espinoza, M and de Silva, R and Tucker, KL and Barde, YA and Duff, K and Davies, P (2003) Hyperphosphorylation and aggregation of tau in mice expressing normal human tau isoforms. J NEUROCHEM , 86 (3) 582 - 590. 10.1046/j.1471-4159.2003.01879.x. |
B
| Baptista, MJ and O'Farrell, C and Daya, S and Ahmad, R and Miller, DW and Hardy, J and Farrer, MJ and Cookson, MR (2003) Co-ordinate transcriptional regulation of dopamine synthesis genes by alpha-synuclein in human neuroblastoma cell lines. JOURNAL OF NEUROCHEMISTRY , 85 (4) 957 - 968. 10.1046/j.1471-4159.2003.01742.x. |
| Baptista, MJ and O'Farrell, C and Hardy, J and Cookson, MR (2003) Microarray analysis reveals induction of heat shock proteins mRNAs by the torsion dystonia protein, TorsinA. NEUROSCIENCE LETTERS , 343 (1) 5 - 8. 10.1016/S0304-3940(03)00302-1. |
| Baumann, M and Mamais, A and McBlane, F and Xiao, H and Boyes, J (2003) Regulation of V(D)J recombination by nucleosome positioning at recombination signal sequences. EMBO J , 22 (19) 5197 - 5207. |
| Brancati, F and Valente, EM and Davies, NP and Sarkozy, A and Sweeney, MG and LoMonaco, M and Pizzuti, A and Hanna, MG and Dallapiccola, B (2003) Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A. J NEUROL NEUROSUR PS , 74 (9) 1339 - 1341. |
C
| Cairns, NJ and Perry, RH and Jaros, E and Burn, D and McKeith, IG and Lowe, JS and Holton, J and Rossor, MN and Skullerud, K and Duyckaerts, C and Cruz-Sanchez, FF and Lantos, PL (2003) Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions. NEUROSCI LETT , 341 (3) 177 - 180. 10.1016/S0304-3940(03)00100-9. |
D
| Davies, NA and Cochrane, G and Hanna, M (2003) Muscle disorders. In: Greenwood, RJ and Barnes, MP and McMillan, TM and Ward, CD, (eds.) Handbook of neurological rehabilitation. (705 - 725). Psychology Press: Hove. |
| Davies, NP and Hanna, MG (2003) The skeletal muscle channelopathies: distinct entities and overlapping syndromes. CURR OPIN NEUROL , 16 (5) 559 - 568. 10.1097/01.wco.0000093098.34793.09. |
| de Silva, R and Hope, A and Pittman, A and Weale, ME and Morris, HR and Wood, NW and Lees, AJ (2003) Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy. NEUROLOGY , 61 (3) 407 - 409. |
| de Silva, R and Lashley, T and Gibb, G and Hanger, D and Hope, A and Reid, A and Bandopadhyay, R and Utton, M and Strand, C and Jowett, T and Khan, N and Anderton, B and Wood, N and Holton, J and Revesz, T and Lees, A (2003) Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies. NEUROPATH APPL NEURO , 29 (3) 288 - 302. |
| de Silva, R. and Lashley, T. and Gibb, G. and Hanger, D. and Hope, A. and Reid, A. and Bandopadhyay, R. and Utton, M. and Strand, C. and Jowett, T. and Khan, N. and Anderton, B. and Wood, N. and Holton, J. and Revesz, T. and Lees, A. (2003) Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies. Neuropathology and Applied Neurobiology , 29 (3) pp. 288-302. 10.1046/j.1365-2990.2003.00463.x. |
| Delisle, MB and Haik, S and Uro-Coste, E and Peoc'h, K and Puel, M and Revesz, T and Piccardo, P and Hauw, JJ and Duyckaerts, C and Laplanche, JL and Ghetti, B (2003) Gerstmann-Straussler-Scheinker disease presenting as corticobasal degeneration. In: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. (pp. 548 - 548). AMER ASSN NEUROPATHOLOGISTS INC |
| Ditzel, M and Wilson, R and Tenev, T and Zachariou, A and Paul, A and Deas, E and Meier, P (2003) Degradation of DIAP1 by the N-end rule pathway is essential for regulating apoptosis. NAT CELL BIOL , 5 (5) 467 - 473. 10.1038/ncb984. |
E
| Edwards, M and Wood, N and Bhatia, K (2003) Unusual phenotypes in DYT1 dystonia: A report of five cases and a review of the literature. MOVEMENT DISORD , 18 (6) 706 - 711. 10.1002/mds.10411. |
| Edwards, M and Wood, N and Bhatia, K (2003) Unusual phenotypes in DYT1 dystonia: A report of five cases and a review of the literature. Movement Disorders , 18 (6) 706 - 711. |
| Edwards, M.J. and Huang, Y.-Z. and Wood, N.W. and Rothwell, J.C. and Bhatia, K.P. (2003) Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation. Brain , 126 (9) pp. 2074-2080. 10.1093/brain/awg209. |
| Edwards, MJ and Huang, YZ and Wood, NW and Rothwell, JC and Bhatia, KP (2003) Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation. BRAIN , 126 2074 - 2080. 10.1093/brain/awg209. |
| Eerola, J and Hernandez, D and Launes, J and Hellstrom, O and Hague, S and Gulick, C and Johnson, J and Peuralinna, T and Hardy, J and Tienari, PJ and Singleton, AB (2003) Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD. NEUROLOGY , 61 (7) 1000 - 1002. |
| El-Agnaf, OMA and Salem, SA and Paleologou, KE and Cooper, LJ and Fullwood, NJ and Gibson, MJ and Curran, MD and Court, JA and Mann, DMA and Ikeda, S and Cookson, MR and Hardy, J and Allsop, D (2003) alpha-synuclein implicated in Parkinson's disease is present in extracellular biological fluids, including human plasma. FASEB JOURNAL , 17 (11) 1945 - +. 10.1096/fj.03-0098fje. |
F
| Frangione, B and Prelli, F and Ghiso, J and Revesz, T (2003) Familial and sporadic cerebral amyloid angiopathics. In: Korczyn, AD, (ed.) THIRD INTERNATIONAL CONGRESS ON VASCULAR DEMENTIA. (pp. 35 - 46). MEDIMOND S R L |
| Frank, RA and Galasko, D and Hampel, H and Hardy, J and de Leon, MJ and Mehta, PD and Rogers, J and Siemers, E and Trojanowski, JQ (2003) Biological markers for therapeutic trials in Alzheimer's disease - Proceedings of the biological markers working group; NIA initiative on neuroimaging in Alzheimer's disease. NEUROBIOLOGY OF AGING , 24 (4) 521 - 536. 10.1016/S0197-4580(03)00002-2. |
G
| Goldstein, D.B. and Ahmadi, K.R. and Weale, M.E. and Wood, N.W. (2003) Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. Trends in Genetics , 19 (11) pp. 615-622. 10.1016/j.tig.2003.09.006. |
| Goldstein, DB and Ahmadi, KR and Weale, ME and Wood, NW (2003) Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. TRENDS GENET , 19 (11) 615 - 622. 10.1016/j.tig.2003.09.006. |
| Grover, A and England, E and Baker, M and Sahara, N and Adamson, J and Granger, B and Houlden, H and Passant, U and Yen, SH and DeTure, M and Hutton, M (2003) A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathy. EXP NEUROL , 184 (1) 131 - 140. 10.1016/S0014-4886(03)00393-5. |
| Groves, MJ and Schanzer, A and Simpson, AJ and An, SF and Kuo, LT and Scaravilli, F (2003) Profile of adult rat sensory neuron loss, apoptosis and replacement after sciatic nerve crush. J NEUROCYTOL , 32 (2) 113 - 122. |
H
| Hadjivassiliou, M and Grunewald, R and Sharrack, B and Sanders, D and Lobo, A and Williamson, C and Woodroofe, N and Wood, N and Davies-Jones, A (2003) Gluten ataxia in perspective: epidemiology, genetic susceptibility and clinical characteristics. BRAIN , 126 685 - 691. 10.1093/brain/awg050. |
| Hague, S and Rogaeva, E and Hernandez, D and Gulick, C and Singleton, A and Hanson, M and Johnson, J and Weiser, R and Gallardo, M and Ravina, B and Gwinn-Hardy, K and Crawley, A and St George-Hyslop, PH and Lang, AE and Heutink, P and Bonifati, V and Hardy, J and Singleton, A (2003) Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation. ANNALS OF NEUROLOGY , 54 (2) 271 - 274. 10.1002/ana.10663. |
| Hanna, M (2003) Disorders of muscle: introduction. In: Warrell, DA and Cox, TM and Firth, JD and Benz, EJ, (eds.) Oxford Textbook of Medicine. (1216 - 1220). Oxford University Press: Oxford. |
| Hardy, J (2003) Alzheimer's disease: Genetic evidence points to a single pathogenesis. ANNALS OF NEUROLOGY , 54 (2) 143 - 144. 10.1002/ana.10624. |
| Hardy, J (2003) Impact of genetic analysis on Parkinson's disease research. In: MOVEMENT DISORDERS. (pp. S96 - S98). WILEY-LISS |
| Hardy, J (2003) The relationship between amyloid and tau. JOURNAL OF MOLECULAR NEUROSCIENCE , 20 (2) 203 - 206. 10.1385/JMN:20:2:203. |
| Hardy, J (2003) The relationship between Lewy body disease, Parkinson's disease, and Alzheimer's disease. Annals of the New York Academy of Sciences , 991 167 - 170. |
| Hardy, J and Cookson, MR and Singleton, A (2003) Genes and parkinsonism. LANCET NEUROLOGY , 2 (4) 221 - 228. 10.1016/S1474-4422(03)00350-8. |
| Hardy, J and Singleton, A and Gwinn-Hardy, K (2003) Ethnic differences and disease phenotypes. SCIENCE , 300 (5620) 739 - 740. 10.1126/science.300.5620.739. |
| Hargreaves, IP and Heales, SJR and Briddon, A and Lee, PJ and Hanna, MG and Land, JM (2003) Primary pyruvate dehydrogenase E3 binding protein deficiency with mild hyperlactataemia and hyperalaninaemia. J INHERIT METAB DIS , 26 (5) 505 - 506. |
| Harold, D and Peirce, T and Moskvina, V and Myers, A and Jones, S and Hollingworth, P and Moore, P and Lovestone, S and Powell, J and Foy, C and Archer, N and Walter, S and Edmonson, A and McIlroy, S and Craig, D and Passmore, PA and Goate, A and Hardy, J and O'Donovan, M and Williams, J and Liddell, M and Owen, MJ and Jones, L (2003) Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease. HUMAN GENETICS , 113 (3) 258 - 267. 10.1007/s00439-003-0960-2. |
| Hernandez, D and Hanson, M and Singleton, A and Gwinn-Hardy, K and Freeman, J and Ravina, B and Doheny, D and Gallardo, M and Weiser, R and Hardy, J and Singleton, A (2003) Mutation at the SCA17 locus is not a common cause of parkinsonism. PARKINSONISM & RELATED DISORDERS , 9 (6) 317 - 320. 10.1016/S1353-8020(03)00027-0. |
| Hogg, M and Grujic, ZM and Baker, M and Demirci, S and Guillozet, AL and Sweet, AP and Herzog, LL and Weintraub, S and Mesulam, MM and LaPointe, NE and Gamblin, TC and Berry, RW and Binder, LI and de Silva, R and Lees, A and Espinoza, M and Davies, P and Grover, A and Sahara, N and Ishizawa, T and Dickson, D and Yen, SH and Hutton, M and Bigio, EH (2003) The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy. ACTA NEUROPATHOL , 106 (4) 323 - 336. 10.1007/s00401-003-0734-x. |
| Holton, JL and Beesley, C and Winchester, B and Al-Memar, A (2003) Vacuolar myopathy in twin girls. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY , 29 (5) 525 - 525. |
| Hope, AD and de Silva, R and Fischer, DF and Hol, EM and van Leeuwen, FW and Lees, AJ (2003) Alzheimer's associated variant ubiquitin causes inhibition of the 26S proteasome and chaperone expression. J NEUROCHEM , 86 (2) 394 - 404. 10.1046/j.1471-4159.2003.01844.x. |
| Houlden, H and Lincoln, S and Farrer, M and Cleland, PG and Hardy, J and Orrell, RW (2003) Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic. NEUROLOGY , 61 (10) 1423 - 1426. |
| Houlden, H. and Lincoln, S. and Farrer, M. and Cleland, P.G. and Hardy, J. and Orrell, R.W. (2003) Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic. Neurology , 61 (10) pp. 1423-1426. |
I
| Iseki, E and Togo, T and Suzuki, K and Katsuse, O and Marui, W and de Silva, R and Lees, A and Yamamoto, T and Kosaka, K (2003) Dementia with Lewy bodies from the perspective of tauopathy. ACTA NEUROPATHOL , 105 (3) 265 - 270. 10.1007/s00401-002-0644-3. |
J
| Jacques, TS and Eldridge, C and Powell, M and Revesz, T (2003) A mixed glial-neuronal tumour of the IVth ventricle with prominent rosette formation. In: NEUROPATH APPL NEURO. (pp. 525 - 526). BLACKWELL PUBLISHING LTD |
| Janssen, JC and Beck, JA and Campbell, TA and Dickinson, A and Fox, NC and Harvey, RJ and Houlden, H and Rossor, MN and Collinge, J (2003) Early onset familial Alzheimer's disease - Mutation frequency in 31 families. NEUROLOGY , 60 (2) 235 - 239. |
| Josephs, K.A. and Holton, J.L. and Rossor, M.N. and Braendgaard, H. and Ozawa, T. and Fox, N.C. and Petersen, R.C. and Pearl, G.S. and Ganguly, M. and Rosa, P. and Laursen, H. and Parisi, J.E. and Waldemar, G. and Quinn, N.P. and Dickson, D.W. and Revesz, T. (2003) Neurofilament inclusion body disease: a new proteinopathy? Brain , 126 (10) pp. 2291-2303. 10.1093/brain/awg231. |
| Josephs, KA and Holton, JL and Rossor, MN and Braendgaard, H and Ozawa, T and Fox, NC and Petersen, RC and Pearl, GS and Ganguly, M and Laursen, H and Parisi, JE and Waldemar, G and Quinn, NP and Dickson, DW and Revesz, T (2003) Neurofilament inclusion body disease. In: ANNALS OF NEUROLOGY. (pp. S51 - S51). WILEY-LISS |
| Josephs, KA and Holton, JL and Rossor, MN and Braendgaard, H and Ozawa, T and Fox, NC and Petersen, RC and Pearl, GS and Ganguly, M and Rosa, P and Laursen, H and Parisi, JE and Waldemar, G and Quinn, NP and Dickson, DW and Revesz, T (2003) Neurofilament inclusion body disease: a new proteinopathy? BRAIN , 126 2291 - 2303. 10.1093/brain/awg231. |
| Josephs, KA and Holton, JL and Rossor, MN and Braendgaard, H and Petersen, RC and Pearl, GS and Ganguly, M and Parisi, JE and Waldemar, G and Quinn, NP and Dickson, DW and Revesz, T (2003) Neurofilament inclusion body disease: a new proteinopathy. NEUROPATH APPL NEURO , 29 (5) 521 - 521. |
K
| Katsuse, O and Iseki, E and Arai, T and Akiyama, H and Togo, T and Uchikado, H and Kato, M and de Silva, R and Lees, A and Kosaka, K (2003) 4-repeat tauopathy sharing pathological and biochemical features of corticobasal degeneration and progressive supranuclear palsy. ACTA NEUROPATHOL , 106 (3) 251 - 260. 10.1007/s00401-003-0728-8. |
| Khan, N.L. and Graham, E. and Critchley, P. and Schrag, A.E. and Wood, N.W. and Lees, A.J. and Bhatia, K.P. and Quinn, N. (2003) Parkin disease: a phenotypic study of a large case series. Brain , 126 (6) pp. 1279-1292. 10.1093/brain/awg142. |
| Khan, NL and Graham, E and Critchley, P and Schrag, AE and Wood, NW and Lees, AJ and Bhatia, KP and Quinn, N (2003) Parkin disease: a phenotypic study of a large case series. BRAIN , 126 1279 - 1292. 10.1093/brain/awg142. |
| Khan, NL and Wood, NW and Bhatia, KP (2003) Autosomal recessive, DYT2-like primary torsion dystonia - A new family. NEUROLOGY , 61 (12) 1801 - 1803. |
| Kuo, L and Scaravilli, F and Groves, MJ and An, SF (2003) Gene expression of neurotrophins and their receptors in the dorsal root ganglion after axotomy and systemic NT-3 treatment. In: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. (pp. 578 - 578). AMER ASSN NEUROPATHOLOGISTS INC |
| Kuoppamaki, M and Giunti, P and Quinn, N and Wood, NW and Bhatia, KP (2003) Slowly progressive cerebellar ataxia and cervical dystonia: Clinical presentation of a new form of spinocerebellar ataxia? MOVEMENT DISORD , 18 (2) 200 - 206. 10.1002/mds.10308. |
L
| Lee, M.-J. and Stephenson, D.A. and Groves, M.J. and Sweeney, M.G. and Davis, M.B. and An, S.-F. and Houlden, H. and Salih, M.A.M. and Timmerman, V. and De Jonghe, P. and Auer-Grumbach, M. and Di Maria, E. and Scaravilli, F. and Wood, N.W. and Reilly, M.M. (2003) Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene. Human Molecular Genetics , 12 (15) pp. 1917-1925. 10.1093/hmg/ddg198. |
| Lee, MJ and Stephenson, DA and Groves, MJ and Sweeney, MG and Davis, MB and An, SF and Houlden, H and Salih, MAM and Timmerman, V and de Jonghe, P and Auer-Grumbach, M and Di Maria, E and Scaravilli, F and Wood, NW and Reilly, MM (2003) Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene. HUM MOL GENET , 12 (15) 1917 - 1925. 10.1093/hmg/ddg198. |
| Lhatoo, SD and Perunovic, B and Love, S and Houlden, H and Campbell, MJ (2003) Familial idiopathic brain calcification - A new and familial alpha-synucleinopathy? EUR NEUROL , 49 (4) 223 - 226. 10.1159/000070189. |
| Lincoln, S and Wiley, J and Lynch, T and Langston, JW and Chen, R and Lang, A and Rogaeva, E and Munhoz, RP and Harris, J and Marder, K and Klein, C and Bisceglio, G and Hussey, J and West, A and Hulihan, M and Hardy, J and Farrer, M (2003) Parkin-proven disease - Common founders but divergent phenotypes. NEUROLOGY , 60 (10) 1605 - 1610. |
| Lincoln, SJ and Maraganore, DM and Lesnick, TG and Bounds, R and de Andrade, M and Bower, JH and Hardy, JA and Farrer, MJ (2003) Parkin variants in north American Parkinson's disease: Cases and controls. MOVEMENT DISORDERS , 18 (11) 1306 - 1311. 10.1002/mds.10601. |
| Liolitsa, D and Rahman, S and Benton, S and Carr, LJ and Hanna, MG (2003) Is the mitochondrial complex IND5 gene a hot-spot for MELAS causing mutations? ANN NEUROL , 53 (1) 128 - 132. 10.1002/ana.10435. |
| Lohmann, E and Periquet, M and Bonifati, V and Wood, NW and De Michele, G and Bonnet, AM and Fraix, V and Broussolle, E and Horstink, MWIM and Vidailhet, M and Verpillat, P and Gasser, T and Nicholl, D and Teive, H and Raskin, S and Rascol, O and Destee, A and Ruberg, M and Gasparini, F and Meco, G and Agid, Y and Durr, A and Brice, A and French Parkinsons Dis Genetics Stu, and European Consortium Genetic Suscep, (2003) How much phenotypic variation can be attributed to parkin genotype? ANN NEUROL , 54 (2) 176 - 185. 10.1002/ana.10613. |
M
| Maraganore, DM and de Andrade, M and Lesnick, TG and Farrer, MJ and Bower, JH and Hardy, JA and Rocca, WA (2003) Complex interactions in Parkinson's disease: A two-phased approach. MOVEMENT DISORDERS , 18 (6) 631 - 636. 10.1002/mds.10431. |
| Maraganore, DM and Farrer, MJ and Lesnick, TG and de Andrade, M and Bower, JH and Hernandez, D and Hardy, JA and Rocca, WA (2003) Case-control study of the alpha-synuclein interacting protein gene and Parkinson's disease. MOVEMENT DISORDERS , 18 (11) 1233 - 1239. 10.1002/mds.10547. |
| Marlow, L and Canet, RM and Haugabook, SJ and Hardy, JA and Lahiri, DK and Sambamurti, K (2003) APH1, PEN2, and Nicastrin increase A beta levels and gamma-secretase activity. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS , 305 (3) 502 - 509. 10.1016/S0006-291X(03)00797-6. |
| Miller, RF and Shahmanesh, M and Hanna, MG and Unwin, RJ and Schapira, AHV and Weller, IVD (2003) Polyphenotypic expression of mitochondrial toxicity caused by nucleoside reverse transcriptase inhibitors. ANTIVIR THER , 8 (3) 253 - 257. |
| Misbahuddin, A and Placzek, MR and Taanman, JW and Cooper, JM and Warner, TT (2003) Study of mutant and wild type torsin A in human SH-SY5Y cell lines. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 409 - 409). BRITISH MED JOURNAL PUBL GROUP |
| Morris, CM and O'Brien, KK and Gibson, AM and Hardy, JA and Singleton, AB (2003) Polymorphism in the human DJ-1 gene is not associated with sporadic dementia with Lewy bodies or Parkinson's disease. NEUROSCIENCE LETTERS , 352 (2) 151 - 153. 10.1016/S0304-3940(03)01030-9. |
| Morris, HR and Osaki, Y and Holton, J and Lees, AJ and Wood, NW and Revesz, T and Quinn, N (2003) Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP. NEUROLOGY , 61 (1) 102 - 104. |
| Mundy, HR and Jones, SJ and Hobart, JC and Hanna, MG and Lee, PJ (2003) A randomized controlled study of modified cobratoxin in adrenomyeloneuropathy. NEUROLOGY , 61 (4) 528 - 530. |
P
| Payami, H and Nutt, J and Gancher, S and Bird, T and McNeal, MG and Seltzer, WK and Hussey, J and Lockhart, P and Gwinn-Hardy, K and Singleton, AA and Singleton, AB and Hardy, J and Farrer, M (2003) SCA2 may present as levodopa-responsive parkinsonism. MOVEMENT DISORDERS , 18 (4) 425 - 429. 10.1002/mds.10375. |
| Periquet, M and Latouche, M and Lohmann, E and Rawal, N and De Michele, G and Ricard, S and Teive, H and Fraix, V and Vidailhet, M and Nicholl, D and Barone, P and Wood, NW and Raskin, S and Deleuze, JF and Agid, Y and Durr, A and Brice, A and French Parkinsons Dis Genetics Stu, and European Consortium Genetic Suscep, (2003) Parkin mutations are frequent in patients with isolated early-onset parkinsonism. BRAIN , 126 1271 - 1278. 10.1093/brain/awg136. |
| Pickford, F and Onstead, L and Camacho-Prihar, C and Hardy, J and McGowan, E (2003) Expression of mBRI(2) in mice. NEUROSCIENCE LETTERS , 338 (2) 95 - 98. 10.1016/S0304-3940(02)01356-3. |
| Pitt, M and Houlden, H and Jacobs, J and Mok, Q and Harding, B and Reilly, M and Surtees, R (2003) Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1. BRAIN , 126 2682 - 2692. 10.1093/brain/awg278. |
| Pitt, M. and Houlden, H. and Jacobs, J. and Mok, Q. and Harding, B. and Reilly, M. and Surtees, R. (2003) Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1. Brain , 126 (12) pp. 2682-2692. 10.1093/brain/awg278. |
| Plun-Favreau, H and Perret, D and Diveu, C and Froger, J and Chevalier, S and Lelievre, E and Gascan, H and Chabbert, M (2003) Leukemia inhibitory factor (LIF), cardiotrophin-1, and oncostatin M share structural binding determinants in the immunoglobulin-like domain of LIF receptor. J BIOL CHEM , 278 (29) 27169 - 27179. 10.1074/jbc.M303168200. |
| Prime, KP and Edwards, SG and Pakianathan, MR and Holton, JL and Scaravilli, F and Miller, RF (2003) Polymyositis masquerading as mitochondrial toxicity. SEX TRANSM INFECT , 79 (5) 417 - 418. |
| Proukakis, C and Auer-Grumbach, M and Wagner, K and Wilkinson, PA and Reid, E and Patton, MA and Warner, TT and Crosby, AH (2003) Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene. Hum Mutat , 21 (2) 170 - ?. 10.1002/humu.9108. |
| Proukakis, C and Crosby, AH and Auer-Grumbach, M and Wagner, K and Reid, E and Patton, MA and Warner, TT (2003) Screening of the spastin gene in autosomal dominant hereditary spastic paraplegia reveals seven novel mutations. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 406 - 407). BRITISH MED JOURNAL PUBL GROUP |
| Pulkes, T and Liolitsa, D and Nelson, IP and Hanna, MG (2003) Classical mitochondrial phenotypes without mtDNA mutations - The possible role of nuclear genes. NEUROLOGY , 61 (8) 1144 - 1147. |
R
| Revesz, T and Ghiso, J and Holton, JL and Frangione, B (2003) Hereditary amyloidoses with neurodegeneration: familial British dementia and familial Danish dementia. In: Dickson, DW, (ed.) Neurodegeneration: the molecular pathology of dementia and movement disorders. (380 - 385). ISN Neuropath Press: Basel. |
| Revesz, T and Ghiso, J and Lashley, T and Plant, G and Rostagno, A and Frangione, B and Holton, JL (2003) Cerebral amyloid angiopathies: A pathologic, biochemical, and genetic view. J NEUROPATH EXP NEUR , 62 (9) 885 - 898. |
| Revesz, T and Holton, JL (2003) Anatamopathological spectrum of tauopathies. MOVEMENT DISORDERS , 18 S13 - S20. 10.1002/mds.10558. |
| Rippon, GA and Crook, R and Baker, M and Halvorsen, E and Chin, S and Hutton, M and Houlden, H and Hardy, J and Lynch, T (2003) Presenilin 1 mutation in an African American family presenting with atypical Alzheimer dementia. ARCH NEUROL-CHICAGO , 60 (6) 884 - 888. |
S
| Scaravilli, F and Lucas, S and Gray, F and Kuo, L and Hall-Craggs, MA and An, SF and Miller, R (2003) The changing presentation of encephalitis in AIDs. In: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. (pp. 562 - 562). AMER ASSN NEUROPATHOLOGISTS INC |
| Schulze, TG and Hardy, J and McMahon, FJ (2003) Inconsistent designs of association studies: a missed opportunity. MOLECULAR PSYCHIATRY , 8 (9) 770 - 772. 10.1038/sj.mp.4001329. |
| Seemungal, BM and Faldon, M and Revesz, T and Lees, AJ and Zee, DS and Bronstein, AM (2003) Influence of target size on vertical gaze palsy in a pathologically proven case of progressive supranuclear palsy. MOVEMENT DISORD , 18 (7) 818 - 822. 10.1002/mds.10434. |
| Sibbing, D and Trender-Gerhardt, I and Wood, NW and Oertel, WH and Bhatia, KP and Bandmann, O (2003) The promoter region of the Menkes gene ATP7A is not altered in focal or generalized dystonia. ANN NEUROL , 53 (2) 278 - 279. 10.1002/ana.10436. |
| Siddiqui, A and Kerb, R and Weale, ME and Brinkmann, U and Smith, A and Goldstein, DB and Wood, NW and Sisodiya, SM (2003) Association of multidrug resistance in epilepsy with a polymorphism in the drug-transporter gene ABCB1. NEW ENGL J MED , 348 (15) 1442 - 1448. |
| Singleton, AB and Farrer, M and Johnson, J and Singleton, A and Hague, S and Kachergus, J and Hulihan, M and Peuralinna, T and Dutra, A and Nussbaum, R and Lincoln, S and Crawley, A and Hanson, M and Maraganore, D and Adler, C and Cookson, MR and Muenter, M and Baptista, M and Miller, D and Blancato, J and Hardy, J and Gwinn-Hardy, K (2003) alpha-synuclein locus triplication causes Parkinson's disease. SCIENCE , 302 (5646) 841 - 841. 10.1126/science.1090278. |
| Sorajja, P and Sweeney, MG and Chalmers, R and Sachdev, B and Syrris, P and Hanna, M and Wood, ND and McKenna, WJ and Elliott, PM (2003) Cardiac abnormalities in patients with Leber's hereditary optic neuropathy. HEART , 89 (7) 791 - 792. |
| Sultan, R and Hanna, MG and Rahman, S and Isenberg, DA (2003) International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in patients with adult onset disease. Journal of Rheumatology , 43 (1) 49 - 54. |
T
| Tabrizi, SJ and Blamire, AM and Manners, DN and Rajagopalan, B and Styles, P and Schapira, AHV and Warner, TT (2003) Creatine therapy for Huntington's disease: Clinical and MRS findings in a 1-year pilot study. NEUROLOGY , 61 (1) 141 - 142. |
| Tan, LC and Tanner, CM and Chen, R and Chan, P and Farrer, M and Hardy, J and Langston, JW (2003) Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation. MOVEMENT DISORDERS , 18 (7) 758 - 763. 10.1002/mds.10432. |
U
| Ule, J and Jensen, KB and Ruggiu, M and Mele, A and Ule, A and Darnell, RB (2003) CLIP identifies Nova-regulated RNA networks in the brain. Science , 302 1212 - 1215. |
V
| Valente, EM and Misbahuddin, A and Brancati, F and Placzek, MR and Garavaglia, B and Salvi, S and Nemeth, A and Shaw-Smith, C and Nardocci, N and Bentivoglio, AR and Berardelli, A and Eleopra, R and Dallapiccola, B and Warner, TT (2003) Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: Evidence for genetic heterogeneity. MOVEMENT DISORD , 18 (9) 1047 - 1051. 10.1002/mds.10476. |
W
| Warner, TT and Schapira, AHV (2003) Genetic and environmental factors in the cause of Parkinson's disease. ANN NEUROL , 53 S16 - S23. 10.1002/ana.10487. |
| Weale, ME and Depondt, C and Macdonald, SJ and Smith, A and Lai, PS and Shorvon, SD and Wood, NW and Goldstein, DB (2003) Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: Implications for linkage-disequilibrium gene mapping. AM J HUM GENET , 73 (3) 551 - 565. |
| Wilkinson, P.A. and Crosby, A.H. and Turner, C. and Patel, H. and Wood, N.W. and Schapira, A.H. and Warner, T.T. (2003) A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia. Neurology , 61 (2) pp. 235-238. |
| Wilkinson, PA and Crosby, AH and Turner, C and Patel, H and Wood, NW and Schapira, AH and Warner, TT (2003) A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia. NEUROLOGY , 61 (2) 235 - 238. |
| Wilkinson, PA and Hart, PE and Patel, H and Warner, TT and Crosby, AH (2003) SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia. J NEUROL SCI , 216 (1) 43 - 45. 10.1016/S0022-510X(03)00210-7. |
| Wood, N (2003) Principles of genetic counselling. In: EPILEPSIA. (pp. 9 - 9). BLACKWELL PUBLISHING INC |
| Wood, NW (2003) Neurogenetics. In: Fowler, TJ and Scadding, JW, (eds.) Clinical neurology. (119 - 129). Arnold: London. |
| Wood, NW (2003) Ataxic disorders. In: Warrell, DA and Cox, TM and Firth, JD and Benz, EJ, (eds.) Oxford Textbook of Medicine. (1068 - 1074). Oxford University Press: Oxford. |
| Wood, NW (2003) Neurogenetics. In: Warrell, DA and Cox, TM and Firth, JD and Benz, EJ, (eds.) Oxford Textbook of Medicine. (945 - 952). Oxford University Press: Oxford. |
| Worth, PF and Wood, NW (2003) A systematic and structured approach to the investigation of ataxia. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 1166 - 1166). BRITISH MED JOURNAL PUBL GROUP |