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Number of items: 124.
A
| Abbruzzese, G and Agid, Y and Albanese, A and Alf, C and Allen, R and Amar, K and de Andrade, LA and Ang, LC and Angelini, C and Archer, RL and Arunodaya, GR and Baltzan, M and Baral, K and Barnett, H and Bergamasco, B and Berger, M and Bernard, J and Bharucha, NE and Bhatia, K and Blary, N and Black, S and Bodis-Wollner, I and Boyson, SJ and Bral-Kulaksizoglu, I and Brooks, DJ and Brown, JD and Burke, RE and Calne, DOC and Calne, SM and Cardoso, F and Cardozo-Pelaez, F and Chang, YJ and Chen, CC and Chen, RS and Chen, R and Chowdhury, A and Christie, S and Chu, CC and Chu, NS and Clarida, L and Collette, EM and Comella, C and Conneally, PM and Crossman, AR and Csanda, E and Dalmau, J and Dalvi, A and De Feijter, A and Deecke, L and Desai, H and De Ybenes, J and Dihenia, B and Direnfeld, L and Dodel, R and Donat, J and Doudet, D and Duane, DD and Duff, J and Duvoisin, R and Eggert, K and Elble, RJ and Elmer, LW and Emre, M and Fariello, R and Fernendy, HH and Findley, LJ and Fink, S and Freissmuth, M and Friedman, JH and de la Fuente-Fernandez, R and Furtado, S and Furukawa, Y and Galvez-Jimenez, N and Gauthier, S and Gawel, MJ and Gilman, S and Gladstone, RM and Goetz, CG and Gomori, A and Gopinathan, G and Gordin, A and Gorell, JM and Greenamyre, JT and Grimes, DA and Gurvit, H and Guttman, M and Guzman, DA and Hachinski, V and Hanagasi, H and Hardy, J and Harik, SJ and Hassan, MN and Hattori, N and Hauser, RA and Hayashi, H and Heller, GL and Hobson, D and Hochschorner, G and Hortnagel, H and Horowski, R and Howse, DC and Huang, CC and Huk, II and Hurtig, H and Hutton, JT and Jaffe, ME and Jankovic, J and Jardine, M and Jog, M and Johnson, B and Kagamihara, Y and Karagoz, N and Kasper, S and Kato, S and Kebabian, JW and Kertsz, A and Khadilkar, SV and Kirk, A and Kish, S and Kitaguchi, T and Kofman, OS and Koide, R and Komori, T and Kostyuk, PG and Kumar, R and Kuo, HC and Kurlan, R and Kurland, L and Kurtuncu, M and Lalkaka, JA and Lambert, M and Landau, W and Lang, AE and Lassmann, H and Lee, CS and Lees, AJ and Lieberman, A and Litvan, I and Loeb, C and Logan, WJ and Lozano, AM and Lu, CS and Lucy, D and Lynch, T and Manyam, BV and Maraganore, D and Marshall, FT and Martin, WRW and Martin, WE and Mathias, C and Matsubera, S and Mendis, T and Menkes, JH and Metz, LN and Miyazaki, Y and Mizuno, Y and Mohr, E and Moodley, LG and Moore, R and Morris, JL and Muthane, U and Nagaraja, D and Nair, CPV and Narabayashi, H and Nomura, Y and Norris, JW and Obeso, JA and O'Brien, C and Oertel, W and Ohtake, T and Okiyama, R and Ozdemir, C and Pal, PK and Panisset, M and Paty, DW and Paulson, GW and Perlmutter, J and Pfeiffer, RF and Pifl, C and Pincus, JH and Poewe, W and Quinn, N and Rajput, AH and Rajput, A and Ransmayr, G and Rascol, O and Robinson, R and Rocca, WA and Roos, RAC and Rosenfeld, MR and Russell, D and Ruth, TJ and Ryu, SJ and Sachdev, H and Safoschnik, G and Sahin, H and Sanchez-Ramos, J and Satishchandra, P and Schapira, A and Scheltens, and Schmidley, JW and Schnaberth, G and Schneider, E and Schneider, JS and Schutz, W and Seeberger, LC and Segawa, M and Sethi, KD and Shah, A and Shannon, K and Shelton, P and Shihabuddin, B and Shimizu, T and Shinotoh, H and Siddique, T and Siderowf, A and Sieghart, W and Simard, A and Simmonds, DC and Singhal, BS and Sluga, E and Snow, BJ and Soukop, W and Sperk, G and Spieker, S and Steele, JC and Stewart, S and Stoessl, AJ and Subramony, SH and Sundaram, M and Sung, CY and Surya, N and Sweet, RD and Tabbal, SD and Takahashi, H and Taniguchi, M and Tarsy, D and Teravainen, H and Tetrud, JW and Tolosa, E and Tourtellotte, WW and Troupin, AS and Tsui, JKC and Tuite, P and Uc, EY and Ueki, Y and Uitti, R and Uyu, C and van Hilten, JJ and Veerendrakumar, M and Veloso, F and Viallet, F and Voll, C and Vrooman, M and Wang, X and Ward, I and Ward, A and Waters, C and Weng, YH and Wenning, GK and Williams, BJ and Wilson, TW and Wolters, EC and Wooten, FG and Wszolek, Z and Yahr, MD and Yanagisawa, N and Yokochi, F and Young, RR and Yu, CM and Zifko, U (2001) An open letter to the Committee on the Nobel Prize in Medicine. PARKINSONISM & RELATED DISORDERS , 7 (2) 149 - 155. |
| Abraham, R and Myers, A and Wavrant-DeVrieze, F and Hamshere, ML and Thomas, HV and Marshall, H and Compton, D and Spurlock, G and Turic, D and Hoogendoorn, B and Kwon, KM and Petersen, RC and Tangalos, E and Norton, J and Morris, JC and Bullock, R and Liolitsa, S and Lovestone, S and Hardy, J and Goate, A and O'Donovan, M and Williams, J and Owen, MJ and Jones, L (2001) Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease. HUMAN GENETICS , 109 (6) 646 - 652. 10.1007/s00439-001-0614-1. |
| Abramov, AY and Zamaraeva, MV and Hagelgans, AI and Azimov, RR and Krasilnikov, OV (2001) Influence of plant terpenoids on the permeability of mitochondria and lipid bilayers. BBA-BIOMEMBRANES , 1512 (1) 98 - 110. |
| An, SF and Osuntokun, O and Groves, M and Scaravilli, F (2001) Expression of CCR-5/CXCR-4 in spinal cord of patients with AIDS. ACTA NEUROPATHOL , 102 (2) 175 - 180. |
B
| Bandopadhyay, R and de Silva, R and Khan, N and Graham, E and Vaughan, J and Engelender, S and Ross, C and Morris, H and Morris, C and Wood, NW and Daniel, S and Lees, A (2001) No pathogenic mutations in the synphilin-1 gene in Parkinson's disease. NEUROSCI LETT , 307 (2) 125 - 127. |
| Bandopadhyay, R and Orte, C and Lawrenson, JG and Reid, AR and De Silva, S and Allt, G (2001) Contractile proteins in pericytes at the blood-brain and blood-retinal barriers. J NEUROCYTOL , 30 (1) 35 - 44. |
| Bibb, JA and Nishi, A and O'Callaghan, JP and Ule, J and Lan, M and Snyder, GL and Horiuchi, A and Saito, T and Hisanaga, S and Czernik, AJ and Nairn, AC and Greengard, P (2001) Phosphorylation of protein phosphatase inhibitor-1 by Cdk5. J Biol Chem , 276 14490 - 14497. 10.1074/jbc.M007197200. |
| Bird, TD and Jarvik, GP and Wood, NW (2001) Genetic association studies - Genes in search of diseases. NEUROLOGY , 57 (7) 1153 - 1154. |
| Bonifati, V and De Michele, G and Lucking, CB and Durr, A and Fabrizio, E and Ambrosio, G and Vanacore, N and De Mari, M and Marconi, R and Capus, L and Breteler, MMB and Gasser, T and Oostra, B and Wood, N and Agid, Y and Filla, A and Meco, G and Brice, A and Italian PD Genetics Study Grp, and French PD Genetics Study Grp, and European Consortium Genetic Suscep, (2001) The parkin gene and its phenotype. NEUROLOGICAL SCIENCES , 22 (1) 51 - 52. |
C
| Caselli, RJ and Osborne, D and Reiman, EM and Hentz, JG and Barbieri, CJ and Saunders, AM and Hardy, J and Graff-Radford, NR and Hall, GR and Alexander, GE (2001) Preclinical cognitive decline in late middle-aged asymptomatic apolipoprotein E-e4/4 homozygotes: a replication study. JOURNAL OF THE NEUROLOGICAL SCIENCES , 189 (1-2) 93 - 98. 10.1016/S0022-510X(01)00577-9. |
| Chan, D and Fox, NC and Scahill, RI and Crum, WR and Whitwell, JL and Leschziner, G and Rossor, AM and Stevens, JM and Cipolotti, L and Rossor, MN (2001) Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease. ANN NEUROL , 49 (4) 433 - 442. |
| Choi, P and Golts, N and Snyder, H and Chong, M and Petrucelli, L and Hardy, J and Sparkman, D and Cochran, E and Lee, JM and Wolozin, B (2001) Co-association of parkin and alpha-synuclein. NEUROREPORT , 12 (13) 2839 - 2843. 10.1097/00001756-200109170-00017. |
| Crockard, HA and Cheeseman, A and Steel, T and Revesz, T and Holton, JL and Plowman, N and Singh, A and Crossman, J (2001) A multidisciplinary team approach to skull base chondrosarcomas. J NEUROSURG , 95 (2) 184 - 189. |
| Crockard, HA and Steel, T and Plowman, N and Singh, A and Crossman, J and Revesz, T and Holton, JL and Cheeseman, A (2001) A multidisciplinary team approach to skull base chordomas. J NEUROSURG , 95 (2) 175 - 183. |
D
| Davenport, WJ and Siegel, AM and Dichgans, J and Drigo, P and Mammi, I and Pereda, P and Wood, NW and Rouleau, GA (2001) CCM1 gene mutations in families segregating cerebral cavernous malformations. NEUROLOGY , 56 (4) 540 - 543. |
| Davies, NP and Eunson, LH and Samuel, M and Hanna, MG (2001) Sodium channel gene mutations in hypokalemic periodic paralysis: An uncommon cause in the UK. NEUROLOGY , 57 (7) 1323 - 1325. |
| Davies, NP and Hanna, MG (2001) Inherited muscle and brain channelopathies. Expert Rev Neurother , 1 (2) 247 - 265. 10.1586/14737175.1.2.247. |
| Davies, NP and Hanna, MG (2001) The skeletal muscle channelopathies: basic science, clinical genetics and treatment. CURR OPIN NEUROL , 14 (5) 539 - 551. |
| Davies, NP and Hanna, MG (2001) The skeletal muscle channelopathies: basic science, clinical genetics and treatment (vol 14, pg 541, 2001). CURRENT OPINION IN NEUROLOGY , 14 (6) 845 - 845. |
| Davies, NP and Hanna, MG (2001) The genetic neurological channelopathies. In: Scolding, N, (ed.) Contemporary treatments in neurology. (398 - 440). Butterworth-Heinemann: Oxford. |
| de Silva, R and Weiler, M and Morris, HR and Martin, ER and Wood, NW and Lees, AJ (2001) Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy. NEUROSCI LETT , 311 (3) 145 - 148. |
| Dickson, D and Farrer, M and Lincoln, S and Mason, RP and Zimmerman, TR and Golbe, LI and Hardy, J (2001) Pathology of PD in monozygotic twins with a 20-year discordance interval. NEUROLOGY , 56 (7) 981 - 982. |
F
| Farrer, M and Chan, P and Chen, R and Tan, L and Lincoln, S and Hernandez, D and Forno, L and Gwinn-Hardy, K and Petrucelli, L and Hussey, J and Singleton, A and Tanner, C and Hardy, J and Langston, JW (2001) Lewy bodies and parkinsonism in families with parkin mutations. ANNALS OF NEUROLOGY , 50 (3) 293 - 300. 10.1002/ana.1132. |
| Farrer, M and Destee, A and Levecque, C and Singleton, A and Engelender, S and Becquet, E and Mouroux, V and Richard, F and Defebvre, L and Crook, R and Hernandez, D and Ross, CA and Hardy, J and Amouyel, P and Chartier-Harlin, MC (2001) Genetic analysis of synphilin-1 in familial Parkinson's disease. NEUROBIOLOGY OF DISEASE , 8 (2) 317 - 323. 10.1006/nbdi.2000.0326. |
| Farrer, M and Maraganore, DM and Lockhart, P and Singleton, A and Lesnick, TG and de Andrade, M and West, A and de Silva, R and Hardy, J and Hernandez, D (2001) alpha-synuclein gene haplotypes are associated with Parkinson's disease. HUM MOL GENET , 10 (17) 1847 - 1851. |
| Farrer, M and Maraganore, DM and Lockhart, P and Singleton, A and Lesnick, TG and De Andrade, M and West, A and De Silva, R and Hardy, J and Hernandez, D (2001) α-synuclein gene haplotypes are associated with Parkinson's disease. Human Molecular Genetics , 10 (17) 1847 - 1851. |
| Feliciani, M and Warner, T (2001) Cervical dystonia. In: The Year in Neurology 2001. (1 - 50). Oxford Clinical Publishing Services |
| Frangione, B and Revesz, T and Vidal, R and Holton, J and Lashley, T and Houlden, H and Wood, N and Rostagno, A and Plant, G and Ghiso, J (2001) Familial cerebral amyloid angiopathy related to stroke and dementia. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS , 8 36 - 42. |
G
| Gaspar, C and Lopes-Cendes, I and Hayes, S and Goto, J and Arvidsson, K and Dias, A and Silveira, I and Maciel, P and Coutinho, P and Lima, M and Zhou, YX and Soong, BW and Watanabe, M and Giunti, P and Stevanin, G and Riess, O and Sasaki, H and Hsieh, M and Nicholson, GA and Brunt, E and Higgins, JJ and Lauritzen, M and Tranebjaerg, L and Volpini, V and Wood, N and Ranum, L and Tsuji, S and Brice, A and Sequeiros, J and Rouleau, GA (2001) Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study. AM J HUM GENET , 68 (2) 523 - 528. |
| Gasser, T and Dichgans, M and Finsterer, J and Hausmanowa-Petrusewicz, I and Jurkat-Rott, K and Klopstock, T and LeGuern, E and Lehesjoki, AE and Lehmann-Horn, F and Lynch, T and Morris, H and Rossor, M and Steinlein, OK and Wood, N and Zaremba, J and Zeviani, M and Zoharn, A and EFNS Task Force on Molecular Diagnosis of Neurologic Disorders, (2001) EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. First of two parts. Eur J Neurol , 8 (4) 299 - 314. |
| Gasser, T and Dichgans, M and Finsterer, J and Hausmanowa-Petrusewicz, I and Jurkat-Rott, K and Klopstock, T and Leguern, E and Lehesjoki, AE and Lehmann-Horn, F and Lynch, T and Morris, H and Rossor, M and Steinlein, OK and Wood, N and Zaremba, J and Zeviani, M and Zoharn, A and EFNS Task Force on Molecular Diagnosis of Neurologic Disorders, (2001) EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. Second of two parts. Eur J Neurol , 8 (5) 407 - 424. |
| Ghiso, J and Revesz, T and Holton, J and Rostagno, A and Lashley, T and Houlden, H and Gibb, G and Anderton, B and Bek, T and Bojsen-Moller, M and Wood, N and Vidal, R and Braenagaard, H and Plant, G and Frangione, B (2001) Review - Chromosome 13 dementia syndromes as models of neurodegeneration. AMYLOID , 8 (4) 277 - 284. |
| Ghiso, J and Revesz, T and Rostagno, A and Vidal, RG and Plant, G and Frangione, B (2001) Familial British dementia. In: Iqbal, K and Sisodia, SS and Winblad, B, (eds.) ALZHEIMER'S DISEASE. (pp. 487 - 493). JOHN WILEY & SONS LTD |
| Ghiso, JA and Holton, J and Miravalle, L and Calero, M and Lashley, T and Vidal, R and Houlden, H and Wood, N and Neubert, TA and Rostagno, A and Plant, G and Revesz, T and Frangione, B (2001) Systemic amyloid deposits in familial British dementia. J BIOL CHEM , 276 (47) 43909 - 43914. |
| Goerres, GW and Revesz, T and Duncan, J and Banati, RB (2001) Imaging cerebral vasculitis in refractory epilepsy using [C-11](R)-PK11195 positron emission tomography. AM J ROENTGENOL , 176 (4) 1016 - 1018. |
| Guerin, CJ and Nolan, CC and Mavroudis, G and Lister, T and Davidson, GM and Holton, JL and Ray, DE (2001) The dynamics of blood-brain barrier breakdown in an experimental model of glial cell degeneration. Neuroscience , 103 (4) 873 - 883. |
| Gwinn-Hardy, K and Singleton, A and O'Suilleabhain, P and Boss, M and Nicholl, D and Adam, A and Hussey, J and Critchley, P and Hardy, J and Farrer, M (2001) Spinocerebellar ataxia type 3 phenotypically resembling Parkinson disease in a black family. ARCHIVES OF NEUROLOGY , 58 (2) 296 - 299. 10.1001/archneur.58.2.296. |
H
| Hall, C. and Brown, M. and Jacobs, T. and Ferrari, G. and Cann, N. and Teo, M. and Monfries, C. and Lim, L. (2001) Collapsin response mediator protein switches RhoA and Rac1 morphology in N1E-115 neuroblastoma cells and is regulated by Rho kinase. Journal of Biological Chemistry , 276 (46) pp. 43482-43486. 10.1074/jbc.C100455200. |
| Hall, C. and Michael, G.J. and Cann, N. and Ferrari, G. and Teo, M. and Jacobs, T. and Monfries, C. and Lim, L. (2001) alpha 2-chimaerin, a Cdc42/Rac1 regulator, is selectively expressed in the rat embryonic nervous system and is involved in neuritogenesis in N1E-115 neuroblastoma cells. The Journal of Neuroscience , 21 (14) pp. 5191-5202. |  |
| Hardy, J (2001) Genetic dissection of neurodegenerative disease. CLINICAL NEUROSCIENCE RESEARCH , 1 (1-2) , Article PII S1566-2772(00)00013-X. 10.1016/S1566-2772(00)00013-X. |
| Hardy, J (2001) The human genome is sequenced - What does it mean and why is it important? ARCHIVES OF NEUROLOGY , 58 (11) 1748 - 1749. 10.1001/archneur.58.11.1748. |
| Hardy, J and Crook, R (2001) Presenilin mutations line up along transmembrane alpha-helices. NEUROSCIENCE LETTERS , 306 (3) 203 - 205. 10.1016/S0304-3940(01)01910-3. |
| Holton, J.L. and Ghiso, J. and Lashle, T. and Rostagno, A. and Guerin, C.J. and Gibb, G. and Houlden, H. and Ayling, H. and Martinian, L. and Anderton, B.H. and Wood, N.W. and Vidal, R. and Plant, G. and Frangione, B. and Revesz, T. (2001) Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia. American Journal of Pathology , 158 (2) pp. 515-526. | |
| Holton, JL and Ghiso, J and Lashley, T and Rostagno, A and Guerin, CJ and Gibb, G and Houlden, H and Ayling, H and Martinian, L and Anderton, BH and Wood, NW and Vidal, R and Plant, G and Frangione, B and Revesz, T (2001) Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia. AM J PATHOL , 158 (2) 515 - 526. |
| Holton, JL and Lashley, T and Vidal, R and Rostagno, A and Gibb, G and Anderton, BH and Braendgaard, H and Plant, GT and Bojsen-Moller, M and Ghiso, J and Frangione, B and Revesz, T (2001) Familial Danish dementia (FDD); A novel form of cerebral amyloidosis associated with deposition of two amyloidogenic peptides. J NEUROPATH EXP NEUR , 60 (5) 536 - 536. |
| Houlden, H and Baker, M and Morris, HR and MacDonald, N and Pickering-Brown, S and Adamson, J and Lees, AJ and Rossor, MN and Quinn, NP and Kertesz, A and Khan, MN and Hardy, J and Lantos, PL and George-Hyslop, PS and Munoz, DG and Mann, D and Lang, AE and Bergeron, C and Bigio, EH and Litvan, I and Bhatia, KP and Dickson, D and Wood, NW and Hutton, M (2001) Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype. NEUROLOGY , 56 (12) 1702 - 1706. |
| Houlden, H and Crook, R and Dolan, RJ and McLaughlin, J and Revesz, T and Hardy, J (2001) A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodies. NEUROSCI LETT , 313 (1-2) 93 - 95. |
| Houlden, H and King, RHM and Hashemi-Nejad, A and Wood, NW and Mathias, CJ and Reilly, M and Thomas, PK (2001) A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V. ANN NEUROL , 49 (4) 521 - 525. |
| Houlden, H and King, RHM and Wood, NW and Thomas, PK and Reilly, MM (2001) Mutations in the 5 ' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin. BRAIN , 124 907 - 915. |
| Houlden, H. and King, R.H.M. and Hashemi-Nejad, A. and Wood, N.W. and Mathias, C.J. and Reilly, M. and Thomas, P.K. (2001) A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V. Annals of Neurology , 49 (4) pp. 521-525. 10.1002/ana.103. |
| Houlden, H. and King, R.H.M. and Wood, N.W. and Thomas, P.K. and Reilly, M.M. (2001) Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin. Brain , 124 (5) pp. 907-915. 10.1093/brain/124.5.907. |
J
| Jackson, TL and Antcliff, RJ and Hodgetts, A and Hussain, AA and Hillenkamp, J and Zhang, JJ and Marshall, J (2001) Retinal exclusion limit: Species variation. INVEST OPHTH VIS SCI , 42 (4) S193 - S193. |
| Jouvenceau, A and Eunson, LH and Spauschus, A and Ramesh, V and Zuberi, SM and Kullmann, DM and Hanna, MG (2001) Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel. LANCET , 358 (9284) 801 - 807. |
| Jouvenceau, A. and Eunson, L.H. and Spauschus, A. and Ramesh, V. and Zuberi, S.M. and Kullmann, D.M. and Hanna , M.G. (2001) Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel. The Lancet , 358 (9284) pp. 801-807. 10.1016/S0140-6736(01)05971-2. |
K
| Khan, N and Graham, E and Dixon, P and Morris, C and Mander, A and Clayton, D and Vaughan, J and Quinn, N and Lees, A and Daniel, S and Wood, N and de Silva, R (2001) Parkinson's disease is not associated with combined alpha-synuclein/apolipoprotein E susceptibility genotype. ANN NEUROL , 49 (5) 665 - 668. |
| Kornek, B and Storch, MK and Bauer, J and Djamshidian, A and Weissert, R and Wallstroem, E and Stefferl, A and Zimprich, F and Olsson, T and Linington, C and Schmidbauer, M and Lassmann, H (2001) Distribution of a calcium channel subunit in dystrophic axons in multiple sclerosis and experimental autoimmune encephalomyelitis. BRAIN , 124 1114 - 1124. |
L
| Le, TV and Crook, R and Hardy, J and Dickson, DW (2001) Cotton wool plaques in non-familial late-onset Alzheimer disease. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY , 60 (11) 1051 - 1061. |
| Lee, MF and Sweeney, M and Stephenson, D and Davis, M and Houlden, H and Wood, NW and Scaravilli, F and Reilly, MM (2001) Genetic study of the mutilated foot rat, an animal model for human hereditary sensory neuropathy. ANN NEUROL , 50 (3) S51 - S51. |
| Lelievre, E and Plun-Favreau, H and Chevalier, S and Froger, J and Guillet, C and Elson, GCA and Gauchat, JF and Gascan, H (2001) Signaling pathways recruited by the cardiotrophin-like cytokine/cytokine-like factor-1 composite cytokine - Specific requirement of the membrane-bound form of ciliary neurotrophic factor receptor alpha component. J BIOL CHEM , 276 (25) 22476 - 22484. |
| Leonard, A.J. and Evans, I.M. and Pickard, M.R. and Bandopadhyay, R. and Sinha, A.K. and Ekins, R.P. (2001) Thyroid hormone receptor expression in rat placenta. Placenta , 22 (4) pp. 353-359. 10.1053/plac.2000.0617. |
| Leonard, AJ and Evans, IM and Pickard, MR and Bandopadhyay, R and Sinha, AK and Ekins, RP (2001) Thyroid hormone receptor expression in rat placenta. PLACENTA , 22 (4) 353 - 359. |
| Lewis, J and Dickson, DW and Lin, WL and Chisholm, L and Corral, A and Jones, G and Yen, SH and Sahara, N and Skipper, L and Yager, D and Eckman, C and Hardy, J and Hutton, M and McGowan, E (2001) Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP. SCIENCE , 293 (5534) 1487 - 1491. 10.1126/science.1058189. |
| Lewis, PA and Piper, S and Baker, M and Onstead, L and Murphy, MP and Hardy, J and Wang, R and McGowan, E and Golde, TE (2001) Expression of BRI-amyloid beta peptide fusion proteins: a novel method for specific high-level expression of amyloid beta peptides. Biochim Biophys Acta , 1537 (1) 58 - 62. |
| Liu, F and Ma, XH and Ule, J and Bibb, JA and Nishi, A and DeMaggio, AJ and Yan, Z and Nairn, AC and Greengard, P (2001) Regulation of cyclin-dependent kinase 5 and casein kinase 1 by metabotropic glutamate receptors. Proc Natl Acad Sci U S A , 98 11062 - 11068. 10.1073/pnas.191353898. |
| Liu, WK and Le, TV and Adamson, J and Baker, M and Cookson, N and Hardy, J and Hutton, M and Yen, SH and Dickson, DW (2001) Relationship of the extended tau haplotype to tau biochemistry and neuropathology in progressive supranuclear palsy. ANNALS OF NEUROLOGY , 50 (4) 494 - 502. 10.1002/ana.1159. |
M
| Maraganore, DM and Hernandez, DG and Singleton, AB and Fatter, MJ and McDonnell, SK and Hutton, ML and Hardy, JA and Rocca, WA (2001) Case-control study of the extended tau gene haplotype in Parkinson's disease. ANNALS OF NEUROLOGY , 50 (5) 658 - 661. 10.1002/ana.1228. |
| Matsuoka, Y and Vila, M and Lincoln, S and McCormack, A and Picciano, M and LaFrancois, J and Yu, X and Dickson, D and Langston, WJ and McGowan, E and Farrer, M and Hardy, J and Duff, K and Przedborski, S and Di Monte, DA (2001) Lack of nigral pathology in transgenic mice expressing human alpha-synuclein driven by the tyrosine hydroxylase promoter. NEUROBIOLOGY OF DISEASE , 8 (3) 535 - 539. 10.1006/nbdi.2001.0392. |
| McEntagart, M and Norton, N and Williams, H and Teare, MD and Dunstan, M and Baker, P and Houlden, H and Reilly, M and Wood, N and Harper, PS and Futreal, PA and Williams, N and Rahman, N (2001) Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14. AM J HUM GENET , 68 (5) 1270 - 1276. |
| McEntagart, M. and Norton, N. and Williams, H. and Teare, M.D. and Dunstan, M. and Baker, P. and Houlden, H. and Reilly, M. and Wood, N. and Harper, P.S. and Futreal, P.A. and Williams, N. and Rahman, N. (2001) Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14. The American Journal of Human Genetics , 68 (5) pp. 1270-1276. 10.1086/320122. |
| Mead, SH and Proukakis, C and Wood, N and Crosby, AH and Plant, GT and Warner, TT (2001) A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members. J NEUROL NEUROSUR PS , 71 (6) 788 - 791. |
| Meschia, JF and Brown, RD and Brott, TG and Hardy, J and Atkinson, EJ and O'Brien, PC (2001) Feasibility of an affected sibling pair study in ischemic stroke - Results of a 2-center family history registry. STROKE , 32 (12) 2939 - 2941. |
| Misbahuddin, A and Warner, TT (2001) Dystonia: an update on genetics and treatment. CURR OPIN NEUROL , 14 (4) 471 - 475. |
| Morris, HR and Al-Sarraj, S and Schwab, C and Gwinn-Hardy, K and Perez-Tur, J and Wood, NW and Hardy, J and Lees, AJ and McGeer, PL and Daniel, SE and Steele, JC (2001) A clinical and pathological study of motor neurone disease on Guam. BRAIN , 124 2215 - 2222. |
| Morris, HR and Khan, MN and Janssen, JC and Brown, JM and Perez-Tur, J and Baker, M and Ozansoy, M and Hardy, J and Hutton, M and Wood, NW and Lees, AJ and Revesz, T and Lantos, P and Rossor, MN (2001) The genetic and pathological classification of familial frontotemporal dementia. ARCH NEUROL-CHICAGO , 58 (11) 1813 - 1816. |
| Morris, HR and Schrag, A and Nath, U and Burn, D and Quinn, NP and Daniel, S and Wood, NW and Lees, AJ (2001) Effect of ApoE and tau on age of onset of progressive supranuclear palsy and multiple system atrophy. NEUROSCI LETT , 312 (2) 118 - 120. |
| Myllykangas, L and Polvikoski, T and Sulkava, R and Notkola, IL and Rastas, S and Verkkoniemi, A and Tienari, PJ and Niinisto, L and Hardy, J and Perez-Tur, J and Kontula, K and Haltia, M (2001) Association of lipoprotein lipase Ser447Ter polymorphism with brain infarction: a population-based neuropathological study. ANNALS OF MEDICINE , 33 (7) 486 - 492. 10.3109/07853890109002098. |
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| Nardocci, N and Fernandez-Alvarez, E and Wood, NW and Spacey, SD and Richter, A (2001) The paroxysmal dyskinesias. In: Guerrini, R and Aicardi, J and Andermann, F and Hallett, M, (eds.) Epilepsy and movement disorders. (125 - 139). Cambridge University Press: Cambridge. |
| Nath, U and Ben-Shlomo, Y and Thomson, RG and Morris, HR and Wood, NW and Lees, AJ and Burn, DJ (2001) The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK. BRAIN , 124 1438 - 1449. |
| Noury, AM and Jackson, TL and Hodgetts, A and Marshall, J (2001) Hydraulic conductivity of sclera as a function of age. INVEST OPHTH VIS SCI , 42 (4) S665 - S665. |
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| O'Farrell, C and Murphy, DD and Petrucelli, L and Singleton, AB and Hussey, J and Farrer, M and Hardy, J and Dickson, DW and Cookson, MR (2001) Transfected synphilin-1 forms cytoplasmic inclusions in HEK293 cells. MOLECULAR BRAIN RESEARCH , 97 (1) 94 - 102. 10.1016/S0169-328X(01)00292-3. |
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| Patel, H and Hart, PE and Warner, T and Allen, I and Phillimore, HE and Silver, JR and Wood, NW and Jeffery, S and Patton, MA and Crosby, AH (2001) Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci. AM J MED GENET , 102 (1) 68 - 72. |
| Patel, H and Hart, PE and Warner, TT and Houlston, RS and Patton, MA and Jeffery, S and Crosby, AH (2001) The Silver syndrome variant of hereditary spastic paraplegia maps to 11q12-q14 with evidence for genetic heterogeneity within this subtype. AMERICAN JOURNAL OF HUMAN GENETICS , 69 (4) 512 - 512. |
| Patel, H and Hart, PE and Warner, TT and Houlston, RS and Patton, MA and Jeffery, S and Crosby, AH (2001) The silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype. AMERICAN JOURNAL OF HUMAN GENETICS , 69 (1) 209 - 215. 10.1086/321267. |
| Periquet, M and Lucking, CB and Vaughan, JR and Bonifati, V and Durr, A and De Michele, G and Horstink, MW and Farrer, M and Illarioshkin, SN and Pollak, P and Borg, M and Brefel-Courbon, C and Denefle, P and Meco, G and Gasser, T and Breteler, MMB and Wood, NW and Agid, Y and Brice, A and French Parkinsons Dis Genetics Stu, and European Consortium Genetic Suscep, (2001) Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects. AM J HUM GENET , 68 (3) 617 - 626. |
| Placzek, MR and Misbahuddin, A and Chaudhuri, KR and Wood, NW and Bhatia, KP and Warner, TT (2001) Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor gene. J NEUROL NEUROSUR PS , 71 (2) 262 - 264. |
| Plant, GT and Guerin, CJ and Holton, J and Houlden, H and Braendgaard, H and Bek, T and Ghiso, J and Frangione, B and Revesz, T (2001) Retinal angiopathy in the British and Danish forms of Familial BRI Dementia. INVEST OPHTH VIS SCI , 42 (4) S648 - S648. |
| Plun-Favreau, H and Elson, G and Chabbert, M and Froger, J and deLapeyriere, O and Lelievre, E and Guillet, C and Hermann, J and Gauchat, JF and Gascan, H and Chevalier, S (2001) The ciliary neurotrophic factor receptor alpha component induces the secretion of and is required for functional responses to cardiotrophin-like cytokine. EMBO J , 20 (7) 1692 - 1703. |
| Polvikoski, T and Sulkava, R and Myllykangas, L and Notkola, IL and Niinisto, L and Verkkoniemi, A and Kainulainen, K and Kontula, K and Perez-Tur, J and Hardy, J and Haltia, M (2001) Prevalence of Alzheimer's disease in very elderly people - A prospective neuropathological study. NEUROLOGY , 56 (12) 1690 - 1696. |
| Proukakis, C and Comiskey, C and Reid, E and Wilkinson, P and Rubinsztein, D and Patton, MA and Warner, TT and Crosby, AH (2001) SPG4 (spastin) mutation screening in hereditary spastic paraparesis. AM J HUM GENET , 69 (4) 600 - 600. |
| Pulkes, T and Hanna, MG (2001) Human mitochondrial DNA diseases. ADV DRUG DELIVER REV , 49 (1-2) 27 - 43. |
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| Rampoldi, L and Dobson-Stone, C and Rubio, JP and Danek, A and Chalmers, RM and Wood, NW and Verellen, C and Ferrer, X and Malandrini, A and Fabrizi, GM and Brown, R and Vance, J and Pericak-Vance, M and Rudolf, G and Carre, S and Alonso, E and Manfredi, M and Nemeth, AH and Monaco, AP (2001) A conserved sorting-associated protein is mutant in chorea- acanthocytosis. Nature Genetics , 28 (2) 119 - 120. |
| Rees, J.H. and Hain, S.F. and Johnson, M.R. and Hughes, R.A.C. and Costa, D.C. and Ell, P.J. and Keir, G. and Rudge, P. (2001) The role of [18F]fluoro-2-deoxyglucose-PET scanning in the diagnosis of paraneoplastic neurological disorders. Brain , 124 (11) pp. 2223-2231. 10.1093/brain/124.11.2223. |
| Rees, JH and Balakas, N and Agathonikou, A and Hain, SF and Giovanonni, G and Panayiotopoulos, CP and Luxsuwong, M and Revesz, T (2001) Primary diffuse leptomeningeal gliomatosis simulating tuberculous meningitis. J NEUROL NEUROSUR PS , 70 (1) 120 - 122. |
| Reilly, MM and Lee, MJ and Sweeney, MG and Stephenson, D and Davis, M and Groves, M and Houlden, H and Wood, NW and Scaravilli, F (2001) Genetic analysis of the mutilated foot (mf) rat: an animal model for human hereditary sensory neuropathy. AM J HUM GENET , 69 (4) 501 - 501. |
| Revesz, T and Gray, F and Scaravilli, F (2001) Parkinson's disease. In: Duckett, S and De La Torre, JC, (eds.) Pathology of the aging human nervous system. (264 - 308). Oxford University Press: Oxford. |
| Revesz, T and Lashley, T and Vidal, R and Rostagno, K and Gibb, G and Anderton, BH and Plant, G and Frangione, B and Ghiso, J and Holton, JL (2001) Deposition of amyloid-BRI (ABri) is associated with neurofibrillary degeneration in familial British dementia (FBD). J NEUROPATH EXP NEUR , 60 (5) 536 - 536. |
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| Scaravilli, F and Pang, JT and An, SF and Chamberlain, S (2001) A case of SCA 2 with unusual pathological findings. J NEUROPATH EXP NEUR , 60 (5) 550 - 550. |
| Sheen, VL and Dixon, PH and Fox, JW and Hong, SE and Kinton, L and Sisodiya, SM and Duncan, JS and Dubeau, F and Scheffer, IE and Schachter, SC and Wilner, A and Henchy, R and Crino, P and Kamuro, K and DiMario, F and Berg, M and Kuzniecky, R and Cole, AJ and Bromfield, E and Biber, M and Schomer, D and Wheless, J and Silver, K and Mochida, GH and Berkovic, SF and Andermann, F and Andermann, E and Dobyns, WB and Wood, NW and Walsh, CA (2001) Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. HUM MOL GENET , 10 (17) 1775 - 1783. |
| Smith, CCT and Hyatt, PJ and Stanyer, L and Betteridge, DJ (2001) Platelet secretion of beta-amyloid is increased in hypercholesterolaemia. BRAIN RES , 896 (1-2) 161 - 164. |
| Steiner, H and Revesz, T and Neumann, M and Romig, H and Grim, MG and Pesold, B and Kretzschmar, HA and Hardy, J and Holton, JL and Baumeister, R and Houlden, H and Haass, C (2001) A pathogenic presenilin-1 deletion causes abberrant A beta 42 production in the absence of congophilic amyloid plaques. J BIOL CHEM , 276 (10) 7233 - 7239. |
| Stewart, VC and Heslegrave, AJ and Brown, GC and Clark, JB and Heales, SJR (2001) Glutamate receptor activation mediates nitric oxide dependent damage to neuronal mitochondria. J NEUROCHEM , 78 84 - 84. |
| Sukocheva, OA and Abramov, AY and Levitskaya, JO and Gagelgans, AI and Carpenter, DO (2001) Modulation of intracellular Ca2+ concentration by vitamin B-12 in rat thymocytes. BLOOD CELL MOL DIS , 27 (5) 812 - 824. 10.1006/bcmd.2001.0450. |
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| Valente, EM and Bentivoglio, AR and Cassetta, E and Dixon, PH and Davis, MB and Ferraris, A and Ialongo, T and Frontali, M and Wood, NW and Albanese, A (2001) DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial cervical or upper limb onset. ANN NEUROL , 49 (3) 362 - 366. |
| Valente, EM and Bentivoglio, AR and Cassetta, E and Dixon, PH and Davis, MB and Ferraris, A and Ialongo, T and Frontali, M and Wood, NW and Albanese, A (2001) Identification of a novel primary torsion dystonia loons (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset. NEUROLOGICAL SCIENCES , 22 (1) 95 - 96. |
| Valente, EM and Bentivoglio, AR and Dixon, PH and Ferraris, A and Ialongo, T and Frontali, M and Albanese, A and Wood, NW (2001) Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36. AM J HUM GENET , 68 (4) 895 - 900. |
| Valente, EM and Brancati, F and Ferraris, A and Bentivoglio, AR and Bonifati, V and Vaughan, J and Pizzuti, A and De Michele, G and Caputo, V and Brice, A and Gasser, T and Breteler, M and Oostra, BA and Dallapiccola, B and Wood, NW and European Consortium Genet Suscepti, (2001) PARK6 is a major locus in early-onset parkinsonism. AM J HUM GENET , 69 (4) 500 - 500. |
| Van Paesschen, W and Sisodiya, S and Connelly, A and Duncan, JS and Free, SL and Raymond, AA and Grünewald, RA and Revesz, T and Shorvon, SD and Fish, DR and Stevens, JM and Johnson, CL and Scaravilli, F and Harkness, WFJ and Jackson, GD (2001) Quantitative hippocampal MRI and intractable temporal lobe epilepsy. Neurology , 57 (11 SUPPL. 4) S5 - S12. |
| Van Paesschen, W and Sisodiya, S and Connelly, A and Duncan, JS and Free, SL and Raymond, AA and Grunewald, RA and Revesz, T and Shorvon, SD and Fish, DR and Stevens, JM and Johnson, CL and Scaravilli, F and Harkness, WFJ and Jackson, GD (2001) Quantitative hippocampal MRI and intractable temporal lobe epilepsy. NEUROLOGY , 57 (11) S5 - S12. |
| Vaughan, JR and Davis, MB and Wood, NW (2001) Genetics of Parkinsonism: a review. ANN HUM GENET , 65 111 - 126. |
| Verkkoniemi, A and Kalimo, H and Paetau, A and Somer, M and Iwatsubo, T and Hardy, J and Haltia, M (2001) Variant Alzheimer disease with spastic paraparesis: Neuropathological phenotype. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY , 60 (5) 483 - 492. |
| Vidal, R and Calero, M and Revesz, T and Plant, G and Ghiso, J and Frangione, B (2001) Sequence, genomic structure and tissue expression of Human BRI3, a member of the BRI gene family. GENE , 266 (1-2) 95 - 102. |
| Vidal, RG and Revesz, T and Rostagno, A and Bek, T and Braendgaard, H and Plant, G and Ghiso, J and Frangione, B (2001) A decamer duplication in the BRI gene originates a de novo amyloid peptide that causes dementia in a Danish kindred. In: Iqbal, K and Sisodia, SS and Winblad, B, (eds.) UNSPECIFIED (507 - 513). JOHN WILEY & SONS LTD |
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| Ward, S and Harding, B and Wilkins, P and Harkness, W and Hayward, R and Darling, JL and Thomas, DGT and Warr, T (2001) Gain of 1q and loss of 22 are the most common changes detected by comparative genomic hybridisation in paediatric ependymoma. Genes, Chromosomes and Cancer , 32 (1) 59 - 66. 10.1002/gcc.1167. |
| Warr, T and Ward, S and Burrows, J and Harding, B and Wilkins, P and Harkness, W and Hayward, R and Darling, J and Thomas, D (2001) Identification of extensive genomic loss and gain by comparative genomic hybridisation in malignant astrocytoma in children and young adults. Genes Chromosomes Cancer , 31 (1) 15 - 22. 10.1002/gcc.1113. |
| West, A and Farrer, M and Petrucelli, L and Cookson, M and Lockhart, P and Hardy, J (2001) Identification and characterization of the human parkin gene promoter. JOURNAL OF NEUROCHEMISTRY , 78 (5) 1146 - 1152. 10.1046/j.1471-4159.2001.00512.x. |
| West, AB and Zimprich, A and Lockhart, PJ and Farrer, M and Singleton, A and Holtom, B and Lincoln, S and Hofer, A and Hill, L and Muller-Myhsok, B and Wszolek, ZK and Hardy, J and Gasser, T (2001) Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes. EUROPEAN JOURNAL OF HUMAN GENETICS , 9 (9) 659 - 666. 10.1038/sj.ejhg.5200698. |
| Whinney, D and Kitchen, N and Revesz, T and Brookes, G (2001) Primary malignant melanoma of the cerebellopontine angle. OTOLOGY & NEUROTOLOGY , 22 (2) 218 - 222. |
| Wilcock, DM and Gordon, MN and Ugen, KE and Gottschall, PE and Dicarlo, G and Dickey, C and Boyett, KW and Jantzen, PT and Connor, KE and Melachrino, J and Hardy, J and Morgan, D (2001) Number of A beta inoculations in APP+PS1 transgenic mice influences antibody titers, microglial activation, and congophilic plaque levels. DNA AND CELL BIOLOGY , 20 (11) 731 - 736. 10.1089/10445490152717596. |
| Wilkinson, PA and Bradley, JL and Warner, TT (2001) Friedreich's ataxia presenting as an isolated spastic paraparesis. J NEUROL NEUROSUR PS , 71 (5) 709 - 709. |
| Willis, T and Roper, HP and Houlden, H (2001) Clinical experience of giant axonal neuropathy in two families, each associated with novel mutations in the gigaxonin gene. NEUROMUSCULAR DISORD , 11 (6-7) 662 - 662. |
| Wood, NW and Kinton, L and Hanna, MG (2001) Genetics of the overlap between epilepsy and movement disorders. In: Guerrini, R and Aicardi, J and Andermann, F and Hallett, M, (eds.) Epilepsy and movement disorders. (451 - 464). Cambridge University Press: Cambridge. |
| Worth, PF and Wood, NW (2001) Spinocerebellar ataxia type 12 is rare in the United Kingdom. NEUROLOGY , 56 (3) 419 - 420. |
| Worth, PF and Wood, NW (2001) Genotype to phenotype in the spinocerebellar ataxias. In: Malcom, S and Goodship, J, (eds.) Genotype to phenotype. (165 - 187). Bios Scientific Publishers |
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| Zuberi, SM and Hanna, MG (2001) Ion channels and neurology. ARCH DIS CHILD , 84 (3) 277 - 280. |