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Number of items: 159.

A

Abbruzzese, G; Agid, Y; Albanese, A; Alf, C; Allen, R; Amar, K; ... Zifko, U; + view all (2001) An open letter to the Committee on the Nobel Prize in Medicine. PARKINSONISM & RELATED DISORDERS , 7 (2) 149 - 155.

Abraham, R; Myers, A; Wavrant-DeVrieze, F; Hamshere, ML; Thomas, HV; Marshall, H; ... Jones, L; + view all (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; Zamaraeva, MV; Hagelgans, AI; Azimov, RR; Krasilnikov, OV; (2001) Influence of plant terpenoids on the permeability of mitochondria and lipid bilayers. BBA-BIOMEMBRANES , 1512 (1) 98 - 110.

An, SF; Osuntokun, O; Groves, M; Scaravilli, F; (2001) Expression of CCR-5/CXCR-4 in spinal cord of patients with AIDS. ACTA NEUROPATHOL , 102 (2) 175 - 180.

Annaert, WG; Esselens, C; Baert, V; Boeve, C; Snellings, G; Cupers, P; ... De Strooper, B; + view all (2001) Interaction with telencephalin and the amyloid precursor protein predicts a ring structure for presenilins. Neuron , 32 (4) 579 - 589.

B

Bajaj, NPS; Lees, A; Giovannoni, G; Bhatia, K; Quinn, N; (2001) Movement disorder in Whipple's disease. NEUROLOGY , 56 (8) A119 - A119.

Bandopadhyay, R; de Silva, R; Khan, N; Graham, E; Vaughan, J; Engelender, S; ... Lees, A; + view all (2001) No pathogenic mutations in the synphilin-1 gene in Parkinson's disease. NEUROSCI LETT , 307 (2) 125 - 127.

Bandopadhyay, R; Orte, C; Lawrenson, JG; Reid, AR; De Silva, S; Allt, G; (2001) Contractile proteins in pericytes at the blood-brain and blood-retinal barriers. J NEUROCYTOL , 30 (1) 35 - 44.

Ben Shlomo, Y; Head, J; Lees, A; (2001) Selegiline and mortality in subjects with Parkinson's disease: a longitudinal community study. Neurology , 57 (2) 369 - 369.

Bibb, JA; Nishi, A; O'Callaghan, JP; Ule, J; Lan, M; Snyder, GL; ... Greengard, P; + view all (2001) Phosphorylation of protein phosphatase inhibitor-1 by Cdk5. J Biol Chem , 276 (17) 14490 - 14497. 10.1074/jbc.M007197200. Gold open access

Bird, TD; Jarvik, GP; Wood, NW; (2001) Genetic association studies - Genes in search of diseases. NEUROLOGY , 57 (7) 1153 - 1154.

Bonifati, V; De Michele, G; Lucking, CB; Durr, A; Fabrizio, E; Ambrosio, G; ... European Consortium Genetic Suscep,; + view all (2001) The parkin gene and its phenotype. NEUROLOGICAL SCIENCES , 22 (1) 51 - 52.

Bostantjopoulou, S; Katsarou, Z; Papadimitriou, A; Veletza, V; Hatzigeorgiou, G; Lees, A; (2001) Clinical features of parkinsonian patients with the alpha-synuclein (G209A) mutation. MOVEMENT DISORDERS , 16 (6) 1007 - 1013. 10.1002/mds.1221.

C

Caselli, RJ; Osborne, D; Reiman, EM; Hentz, JG; Barbieri, CJ; Saunders, AM; ... Alexander, GE; + view all (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.

Choi, P; Golts, N; Snyder, H; Chong, M; Petrucelli, L; Hardy, J; ... Wolozin, B; + view all (2001) Co-association of parkin and alpha-synuclein. NEUROREPORT , 12 (13) 2839 - 2843. 10.1097/00001756-200109170-00017.

Cordivari, C; Misra, VP; Catania, S; Lees, AJ; (2001) Treatment of dystonic clenched fist with botulinum toxin. MOVEMENT DISORD , 16 (5) 907 - 913.

Creemers, JW; Ines Dominguez, D; Plets, E; Serneels, L; Taylor, NA; Multhaup, G; ... De Strooper, B; + view all (2001) Processing of beta-secretase by furin and other members of the proprotein convertase family. J Biol Chem , 276 (6) 4211 - 4217. 10.1074/jbc.M006947200.

Crockard, HA; Cheeseman, A; Steel, T; Revesz, T; Holton, JL; Plowman, N; ... Crossman, J; + view all (2001) A multidisciplinary team approach to skull base chondrosarcomas. J NEUROSURG , 95 (2) 184 - 189.

Crockard, HA; Steel, T; Plowman, N; Singh, A; Crossman, J; Revesz, T; ... Cheeseman, A; + view all (2001) A multidisciplinary team approach to skull base chordomas. J NEUROSURG , 95 (2) 175 - 183.

Cupers, P; Bentahir, M; Craessaerts, K; Orlans, I; Vanderstichele, H; Saftig, P; ... Annaert, W; + view all (2001) The discrepancy between presenilin subcellular localization and gamma-secretase processing of amyloid precursor protein. J Cell Biol , 154 (4) 731 - 740. 10.1083/jcb.200104045.

Cupers, P; Orlans, I; Craessaerts, K; Annaert, W; De Strooper, B; (2001) The amyloid precursor protein (APP)-cytoplasmic fragment generated by gamma-secretase is rapidly degraded but distributes partially in a nuclear fraction of neurones in culture. J Neurochem , 78 (5) 1168 - 1178.

D

Davenport, WJ; Siegel, AM; Dichgans, J; Drigo, P; Mammi, I; Pereda, P; ... Rouleau, GA; + view all (2001) CCM1 gene mutations in families segregating cerebral cavernous malformations. NEUROLOGY , 56 (4) 540 - 543.

Davies, NP; Eunson, LH; Samuel, M; Hanna, MG; (2001) Sodium channel gene mutations in hypokalemic periodic paralysis: An uncommon cause in the UK. NEUROLOGY , 57 (7) 1323 - 1325.

Davies, NP; Hanna, MG; (2001) Inherited muscle and brain channelopathies. Expert Rev Neurother , 1 (2) 247 - 265. 10.1586/14737175.1.2.247.

Davies, NP; Hanna, MG; (2001) The skeletal muscle channelopathies: basic science, clinical genetics and treatment. CURR OPIN NEUROL , 14 (5) 539 - 551.

Davies, NP; 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; Hanna, MG; (2001) The genetic neurological channelopathies. In: Scolding, N, (ed.) Contemporary treatments in neurology. (398 - 440). Butterworth-Heinemann: Oxford.

De Jonghe, C; Esselens, C; Kumar-Singh, S; Craessaerts, K; Serneels, S; Checler, F; ... De Strooper, B; + view all (2001) Pathogenic APP mutations near the gamma-secretase cleavage site differentially affect Abeta secretion and APP C-terminal fragment stability. Hum Mol Genet , 10 (16) 1665 - 1671.

de Silva, R; Weiler, M; Morris, HR; Martin, ER; Wood, NW; Lees, AJ; (2001) Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy. NEUROSCI LETT , 311 (3) 145 - 148.

De Strooper, B; Annaert, W; (2001) Presenilins and the intramembrane proteolysis of proteins: Facts and fiction. Nature Cell Biology , 3 (10) 10.1038/ncb1001-e221.

De Strooper, B; Annaert, W; (2001) Where Notch and Wnt signaling meet. The presenilin hub. J Cell Biol , 152 (4) F17 - F20.

De Strooper, B; König, G; (2001) An inflammatory drug prospect. Nature , 414 (6860) 159 - 160. 10.1038/35102656.

Dickson, D; Farrer, M; Lincoln, S; Mason, RP; Zimmerman, TR; Golbe, LI; Hardy, J; (2001) Pathology of PD in monozygotic twins with a 20-year discordance interval. NEUROLOGY , 56 (7) 981 - 982.

Doder, M; Rabiner, EI; Turjanski, N; Lees, AJ; Brooks, DJ; (2001) Functional imaging of tremor in Parkinson's disease with [C-11]-WAY 100635 PET. NEUROLOGY , 56 (8) A271 - A272.

Dominguez, DI; De Strooper, B; Annaert, W; (2001) Secretases as therapeutic targets for the treatment of Alzheimer's disease. Amyloid , 8 (2) 124 - 142.

F

Farrer, M; Chan, P; Chen, R; Tan, L; Lincoln, S; Hernandez, D; ... Langston, JW; + view all (2001) Lewy bodies and parkinsonism in families with parkin mutations. ANNALS OF NEUROLOGY , 50 (3) 293 - 300. 10.1002/ana.1132.

Farrer, M; Destee, A; Levecque, C; Singleton, A; Engelender, S; Becquet, E; ... Chartier-Harlin, MC; + view all (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; Lockhart, P; Singleton, A; West, A; Hardy, J; Hernandez, D; ... De Silva, R; + view all (2001) α-synuclein gene haplotypes are associated with Parkinson's disease. Human Molecular Genetics , 10 (17) 1847 - 1851.

Farrer, M; Maraganore, DM; Lockhart, P; Singleton, A; Lesnick, TG; de Andrade, M; ... Hernandez, D; + view all (2001) alpha-synuclein gene haplotypes are associated with Parkinson's disease. HUM MOL GENET , 10 (17) 1847 - 1851.

Feliciani, M; Warner, T; (2001) Cervical dystonia. In: The Year in Neurology 2001. (1 - 50). Oxford Clinical Publishing Services

Frangione, B; Revesz, T; Vidal, R; Holton, J; Lashley, T; Houlden, H; ... Ghiso, J; + view all (2001) Familial cerebral amyloid angiopathy related to stroke and dementia. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS , 8 36 - 42.

G

Gaspar, C; Lopes-Cendes, I; Hayes, S; Goto, J; Arvidsson, K; Dias, A; ... Rouleau, GA; + view all (2001) Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study. AM J HUM GENET , 68 (2) 523 - 528.

Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; ... EFNS Task Force on Molecular Diagnosis of Neurologic Disorders,; + view all (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; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; ... EFNS Task Force on Molecular Diagnosis of Neurologic Disorders,; + view all (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; Revesz, T; Holton, J; Rostagno, A; Lashley, T; Houlden, H; ... Frangione, B; + view all (2001) Review - Chromosome 13 dementia syndromes as models of neurodegeneration. AMYLOID , 8 (4) 277 - 284.

Ghiso, JA; Holton, J; Miravalle, L; Calero, M; Lashley, T; Vidal, R; ... Frangione, B; + view all (2001) Systemic amyloid deposits in familial British dementia. J BIOL CHEM , 276 (47) 43909 - 43914. Gold open access

Gibson, GE; Kingsbery, AE; Xu, H; Lindsay, JG; Daniel, S; Foster, O; ... Blass, JP; + view all (2001) Deficit in a Krebs cycle mitochondrial enzyme in brains from patients with Parkinson's disease. JOURNAL OF NEUROCHEMISTRY , 78 132 - 132.

Guerin, CJ; Nolan, CC; Mavroudis, G; Lister, T; Davidson, GM; Holton, JL; Ray, DE; (2001) The dynamics of blood-brain barrier breakdown in an experimental model of glial cell degeneration. NEUROSCIENCE , 103 (4) 873 - 883. 10.1016/S0306-4522(01)00015-X.

Gwinn-Hardy, K; Singleton, A; O'Suilleabhain, P; Boss, M; Nicholl, D; Adam, A; ... Farrer, M; + view all (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.; Brown, M.; Jacobs, T.; Ferrari, G.; Cann, N.; Teo, M.; ... Lim, L.; + view all (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. Gold open access

Hall, C.; Michael, G.J.; Cann, N.; Ferrari, G.; Teo, M.; Jacobs, T.; ... Lim, L.; + view all (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. Green open access
file

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; Crook, R; (2001) Presenilin mutations line up along transmembrane alpha-helices. NEUROSCIENCE LETTERS , 306 (3) 203 - 205. 10.1016/S0304-3940(01)01910-3.

Hartmann, D; Tournoy, J; Saftig, P; Annaert, W; De Strooper, B; (2001) Implication of APP secretases in notch signaling. J Mol Neurosci , 17 (2) 171 - 181. 10.1385/JMN:17:2:171.

Holton, J.L.; Ghiso, J.; Lashle, T.; Rostagno, A.; Guerin, C.J.; Gibb, G.; ... Revesz, T.; + view all (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. Green open access
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Holton, JL; Ghiso, J; Lashley, T; Rostagno, A; Guerin, CJ; Gibb, G; ... Revesz, T; + view all (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; Lashley, T; Vidal, R; Rostagno, A; Gibb, G; Anderton, BH; ... Revesz, T; + view all (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; Baker, M; Morris, HR; MacDonald, N; Pickering-Brown, S; Adamson, J; ... Hutton, M; + view all (2001) Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype. NEUROLOGY , 56 (12) 1702 - 1706.

Houlden, H; Crook, R; Dolan, RJ; McLaughlin, J; Revesz, T; 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; King, RHM; Hashemi-Nejad, A; Wood, NW; Mathias, CJ; Reilly, M; 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; King, RHM; Wood, NW; Thomas, PK; 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; Parlette, E; Domínguez, K; Hoffler, KD; Chui, CK; (2001) Development of multi-dimensional wavelet methods for simulation aerodynamic modeling. 39th Aerospace Sciences Meeting and Exhibit

Houlden, H.; King, R.H.M.; Hashemi-Nejad, A.; Wood, N.W.; Mathias, C.J.; Reilly, M.; 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.; King, R.H.M.; Wood, N.W.; Thomas, P.K.; 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.

Hughes, AJ; Ben-Shlomo, Y; Daniel, SE; Lees, AJ; (2001) What features improve the accuracy of clinical diagnosis in Parkinson's disease: A clinicopathologic study. NEUROLOGY , 57 (10) S34 - S38.

Hughes, AJ; Daniel, SE; Lees, AJ; (2001) Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease. NEUROLOGY , 57 (8) 1497 - 1499.

Hughes, AJ; Lees, AJ; Daniel, SE; Ben-Shlomo, Y; (2001) What features improve the accuracy of clinical diagnosis in parkinson's disease: A clinicopathologic study. Neurology , 57 (10 SUPPL. 3) 1142 - 1146.

J

Jouvenceau, A; Eunson, LH; Spauschus, A; Ramesh, V; Zuberi, SM; Kullmann, DM; Hanna, MG; (2001) Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel. LANCET , 358 (9284) 801 - 807.

Jouvenceau, A.; Eunson, L.H.; Spauschus, A.; Ramesh, V.; Zuberi, S.M.; Kullmann, D.M.; 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; Graham, E; Dixon, P; Morris, C; Mander, A; Clayton, D; ... de Silva, R; + view all (2001) Parkinson's disease is not associated with combined alpha-synuclein/apolipoprotein E susceptibility genotype. ANN NEUROL , 49 (5) 665 - 668.

Khan, NL; Pavese, N; Wood, NW; Lees, AJ; Brooks, DJ; Piccini, P; (2001) An 18F dopa PET study of disease progression and subclinical nigrostriatal dysfunction in a Parkin kindred. NEUROLOGY , 56 (8) A249 - A249.

Koller, W; Lees, A; Doder, M; Hely, M; Tolcapone Pergolide Study Grp,; (2001) Randomized trial of tolcapone versus pergolide as add-on to levodopa therapy in Parkinson's disease patients with motor fluctuations. MOVEMENT DISORD , 16 (5) 858 - 866.

L

Lang, AE; Lees, AJ; (2001) Editorial. Movement Disorders , 16 (1) 1 - 2. 10.1002/1531-8257(200101)16:1<1::AID-MDS1015>3.0.CO;2-5.

Lang, AE; Lees, AJ; (2001) Untitled. MOVEMENT DISORDERS , 16 (1) 1 - 2. 10.1002/1531-8257(200101)16:1<1::AID-MDS1015>3.0.CO;2-5.

Le, TV; Crook, R; Hardy, J; 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; Sweeney, M; Stephenson, D; Davis, M; Houlden, H; Wood, NW; ... Reilly, MM; + view all (2001) Genetic study of the mutilated foot rat, an animal model for human hereditary sensory neuropathy. ANN NEUROL , 50 (3) S51 - S51.

Lees, A; (2001) Jumpers. MOVEMENT DISORD , 16 (3) 403 - 404.

Lees, AJ; (2001) Apomorphine infusions for treatment of advanced Parkinson's disease. In: Krauss, JK and Jankovic, J and Grossman, RG, (eds.) Surgery for Parkinson's disease and movement disorders. (252 - 257). Lippincott, Williams & Wilkins: London.

Lees, AJ; Katzenschlager, R; Head, J; Ben-Shlomo, Y; Parkinsons Dis Res Grp United King,; (2001) Ten-year follow-up of three different initial treatments in de-novo PD - A randomized trial. NEUROLOGY , 57 (9) 1687 - 1694.

Lelievre, E; Plun-Favreau, H; Chevalier, S; Froger, J; Guillet, C; Elson, GCA; ... Gascan, H; + view all (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. Gold open access

Leonard, A.J.; Evans, I.M.; Pickard, M.R.; Bandopadhyay, R.; Sinha, A.K.; Ekins, R.P.; (2001) Thyroid hormone receptor expression in rat placenta. Placenta , 22 (4) pp. 353-359. 10.1053/plac.2000.0617.

Leonard, AJ; Evans, IM; Pickard, MR; Bandopadhyay, R; Sinha, AK; Ekins, RP; (2001) Thyroid hormone receptor expression in rat placenta. PLACENTA , 22 (4) 353 - 359.

Lewis, J; Dickson, DW; Lin, WL; Chisholm, L; Corral, A; Jones, G; ... McGowan, E; + view all (2001) Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP. SCIENCE , 293 (5534) 1487 - 1491. 10.1126/science.1058189.

Lewis, PA; Piper, S; Baker, M; Onstead, L; Murphy, MP; Hardy, J; ... Golde, TE; + view all (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; Ma, XH; Ule, J; Bibb, JA; Nishi, A; DeMaggio, AJ; ... Greengard, P; + view all (2001) Regulation of cyclin-dependent kinase 5 and casein kinase 1 by metabotropic glutamate receptors. Proc Natl Acad Sci U S A , 98 (20) 11062 - 11068. 10.1073/pnas.191353898.

Liu, WK; Le, TV; Adamson, J; Baker, M; Cookson, N; Hardy, J; ... Dickson, DW; + view all (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

Manson, AJ; Hanagasi, H; Turner, K; Patsalos, PN; Carey, P; Ratnaraj, N; Lees, AJ; (2001) Intravenous apomorphine therapy in Parkinson's disease - Clinical and pharmacokinetic observations. BRAIN , 124 331 - 340.

Manson, AJ; Katzenschlager, R; Hobart, J; Lees, AJ; (2001) High dose naltrexone for dyskinesias induced by levodopa. J NEUROL NEUROSUR PS , 70 (4) 554 - 556.

Maraganore, DM; Hernandez, DG; Singleton, AB; Fatter, MJ; McDonnell, SK; Hutton, ML; ... Rocca, WA; + view all (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.

Marks, L; Turner, K; O'Sullivan, J; Deighton, B; Lees, A; (2001) Drooling in Parkinson's disease: A novel speech and language therapy intervention. In: INTERNATIONAL JOURNAL OF LANGUAGE & COMMUNICATION DISORDERS. (pp. 282 - 287).

Matsuoka, Y; Vila, M; Lincoln, S; McCormack, A; Picciano, M; LaFrancois, J; ... Di Monte, DA; + view all (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; Norton, N; Williams, H; Teare, MD; Dunstan, M; Baker, P; ... Rahman, N; + view all (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.; Norton, N.; Williams, H.; Teare, M.D.; Dunstan, M.; Baker, P.; ... Rahman, N.; + view all (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; Proukakis, C; Wood, N; Crosby, AH; Plant, GT; 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; Brown, RD; Brott, TG; Hardy, J; Atkinson, EJ; 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; Warner, TT; (2001) Dystonia: an update on genetics and treatment. CURR OPIN NEUROL , 14 (4) 471 - 475.

Morris, HR; Al-Sarraj, S; Schwab, C; Gwinn-Hardy, K; Perez-Tur, J; Wood, NW; ... Steele, JC; + view all (2001) A clinical and pathological study of motor neurone disease on Guam. BRAIN , 124 2215 - 2222.

Morris, HR; Khan, MN; Janssen, JC; Brown, JM; Perez-Tur, J; Baker, M; ... Rossor, MN; + view all (2001) The genetic and pathological classification of familial frontotemporal dementia. ARCH NEUROL-CHICAGO , 58 (11) 1813 - 1816.

Morris, HR; Schrag, A; Nath, U; Burn, D; Quinn, NP; Daniel, S; ... Lees, AJ; + view all (2001) Effect of ApoE and tau on age of onset of progressive supranuclear palsy and multiple system atrophy. NEUROSCI LETT , 312 (2) 118 - 120.

Munchau, A; Bahlke, G; Allen, PJ; Quinn, NP; Lees, AJ; Rothwell, JC; ... Bhatia, KP; + view all (2001) Polymyography combined with time-locked video recording (video EMG) for presurgical assessment of patients with cervical dystonia. EUR NEUROL , 45 (4) 222 - 228.

Munchau, A; Palmer, JD; Dressler, D; O'Sullivan, JD; Tsang, KL; Jahanshahi, M; ... Bhatia, KP; + view all (2001) Prospective study of selective peripheral denervation for botulinum-toxin resistant patients with cervical dystonia. BRAIN , 124 769 - 783.

Myllykangas, L; Polvikoski, T; Sulkava, R; Notkola, IL; Rastas, S; Verkkoniemi, A; ... Haltia, M; + view all (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.

N

Nardocci, N; Fernandez-Alvarez, E; Wood, NW; Spacey, SD; 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.

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T

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V

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This list was generated on Sun Oct 19 07:43:37 2014 BST.