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Number of items: 234.

A

Adlkofer, F; Aguzzi, A; Baumeister, R; Haass, C; Silva, ODE; DeStrooper, B; ... Wiltfang, J; + view all (2002) Early diagnosis of Alzheimer's disease and related dementia (DIADEM) - A research network funded by the European Union. NEUROBIOL AGING , 23 (1) S383 - S383.

Alves, JD; Ames, PRJ; Donohue, S; Stanyer, L; Noorouz-Zadeh, J; Ravirajan, C; Isenberg, DA; (2002) Antibodies to high-density lipoprotein and beta(2)-glycoprotein I are inversely correlated with paraoxonase activity in systemic lupus erythematosus and primary antiphospholipid syndrome. ARTHRITIS RHEUM , 46 (10) 2686 - 2694. 10.1002/art.10542.

Amtul, Z; Lewis, PA; Piper, S; Crook, R; Baker, M; Findlay, K; ... Golde, TE; + view all (2002) A presenilin 1 mutation associated with familial frontotemporal dementia inhibits gamma-secretase cleavage of APP and notch. Neurobiol Dis , 9 (2) 269 - 273. 10.1006/nbdi.2001.0473.

An, SF; Groves, M; Martinian, L; Kuo, LT; Scaravilli, F; (2002) Detection of infectious agents in brain of patients with acute hemorrhagic leukoencephalitis. J NEUROVIROL , 8 (5) 439 - 446. 10.1080/13550280290100798.

Anderson, LVB; Bushby, KMD; Hanna, MG; Muntoni, FN; Hilton-Jones, D; Newsom-Davis, J; (2002) Diagnosing rare neuromuscular diseases - The jump from research to service. In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. S72 - S72).

Annaert, W; De Strooper, B; (2002) A cell biological perspective on Alzheimer's disease. Annu Rev Cell Dev Biol , 18 25 - 51. 10.1146/annurev.cellbio.18.020402.142302.

Asmus, F; Zimprich, A; du Montcel, ST; Kabus, C; Deuschl, G; Kupsch, A; ... Gasser, T; + view all (2002) Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype. ANN NEUROL , 52 (4) 489 - 492. 10.1002/ana.10325.

B

Baekelandt, V; Claeys, A; Eggermont, K; Lauwers, E; De Strooper, B; Nuttin, B; Debyser, Z; (2002) Characterization of lentiviral vector-mediated gene transfer in adult mouse brain. Hum Gene Ther , 13 (7) 841 - 853. 10.1089/10430340252899019.

Bajaj, NPS; Waldman, A; Orrell, R; Wood, NW; Bhatia, KP; (2002) Familial adult onset of Krabbe's disease resembling hereditary spastic paraplegia with normal neuroimaging. J NEUROL NEUROSUR PS , 72 (5) 635 - 638.

Bandmann, O; Wood, NW; (2002) Dopa-responsive dystonia -- the story so far. Neuropediatrics , 33 (1) 1 - 5.

Ben-Shlomo, Y; Camfield, L; Warner, T; Grp, ESDEC; (2002) What are the determinants of quality of life in people with cervical dystonia? JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 72 (5) 608 - 614. 10.1136/jnnp.72.5.608.

Bensimon, G; Leigh, PN; Ludolph, A; Lacomblez, L; Vidailhet, M; Landwehrmeyer, B; ... Grp, NNIPPSS; + view all (2002) Neuroprotection and Natural History in Parkinson Plus Syndromes (NNIPPS): Design and progress report of a clinical trial of the efficacy and safety of riluzole in Progressive Supranuclear Palsy (PSP) and Multiple System Atrophy (MSA). In: MOVEMENT DISORDERS. (pp. S256 - S256).

Bloem, BR; Mazibrada, G; Schrag, A; Viswanathan, R; Lees, AJ; Quinn, NP; (2002) Falls and injuries in Progressive Supranuclear Palsy (PSP). In: MOVEMENT DISORDERS. (pp. S252 - S252).

Boeve, BF; Maraganore, DM; Parisi, JE; Ivnik, RJ; Westmoreland, BF; Dickson, DW; ... Petersen, RC; + view all (2002) Corticobasal degeneration and frontotemporal dementia presentations in a kindred with nonspecific histopathology. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS , 13 (2) 80 - 90. 10.1159/000048638.

Brealey, D.; Brand, M.; Hargreaves, I.; Heales, S.; Land, J.; Smolenski, R.; ... Singer, M.; + view all (2002) Association between mitochondrial dysfunction and severity and outcome of septic shock. The Lancet , 360 (9328) pp. 219-223. 10.1016/S0140-6736(02)09459-X.

Burn, DJ; Lees, AJ; (2002) Progressive supranuclear palsy: Where are we now? Lancet Neurology , 1 (6) 359 - 369. 10.1016/S1474-4422(02)00161-8.

C

Camfield, L; Ben-Shlomo, Y; Warner, TT; Epidemiological Study Dystonia Eur,; (2002) Impact of cervical dystonia on quality of life. MOVEMENT DISORD , 17 (4) 838 - 841. 10.1002/mds.10127.

Caparros-Lefebvre, D; Sergeant, N; Lees, A; Camuzat, A; Daniel, S; Lannuzel, A; ... Duyckaerts, C; + view all (2002) Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy. BRAIN , 125 801 - 811.

Caselli, RJ; Hentz, JG; Osborne, D; Graff-Radford, NR; Barbieri, CJ; Alexander, GE; ... Saunders, AM; + view all (2002) Apolipoprotein E and intellectual achievement. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY , 50 (1) 49 - 54. 10.1046/j.1532-5415.2002.50007.x.

Cenci, AM; Andersson, M; Daniel, SE; Kingsbury, AE; Kilford, L; Lees, AJ; (2002) Striatal expression of FosB-related transcription factors in human Parkinson's disease: Relation to L-dopa-induced dyskinesia. In: MOVEMENT DISORDERS. (pp. S98 - S98).

Chinnery, PF; Walls, TJ; Hanna, MG; Bates, D; Fawcett, PRW; (2002) Normokalemic periodic paralysis revisited: Does it exist? ANN NEUROL , 52 (2) 251 - 252. 10.1002/ana.10257.

Chong, MS; Smith, TE; Hanna, M; (2002) Case reports - reversal of sensory deficit associated with pain relief after treatment with gabapentin. PAIN , 96 (3) , Article PII S0304-3959(01)00468-7. 10.1016/S0304-3959(01)00468-7.

Church, AJ; Cardoso, F; Dale, RC; Lees, AJ; Thompson, EJ; Giovannoni, G; (2002) Anti-basal ganglia antibodies in acute and persistent Sydenham's chorea. NEUROLOGY , 59 (2) 227 - 231.

Colosimo, C; Hughes, AJ; Kilford, L; Lees, AJ; (2002) Lewy body cortical involvement may not always predict dementia in Parkinson's disease. In: MOVEMENT DISORDERS. (pp. S134 - S134).

Colosimo, C; Osaki, Y; Vanacore, N; Lees, AJ; (2002) Lack of association between progressive supranuclear palsy and arterial hypertension: A clinico-pathological study. In: MOVEMENT DISORDERS. (pp. S254 - S255).

Compton, D; DeVrieze, FW; Petersen, RC; Tangalos, E; Li, L; Hardy, J; (2002) Possible association between genetic variability at the apolipoprotein(a) locus and Alzheimer's disease in apolipoprotein E2 carriers. NEUROSCI LETT , 331 (1) 60 - 62.

Cordivari, C; (2002) Botulinum toxins in the treatment of limb dystonia. In: OPTIMAL PATIENT MANAGEMENT WITH BOTULINUM TOXINS: EVIDENCE AND EXPERIENCE. (pp. 55 - 63).

Cordivari, C; Lees, AJ; Misra, P; Brown, P; (2002) EMG-EMG coherence in writer's cramp. MOVEMENT DISORD , 17 (5) 1011 - 1016. 10.1002/mds.10212.

Cordivari, C; Vincent, A; Misra, VP; Catania, S; Bhatia, KP; Lees, AJ; (2002) Patients with cervical dystonia thought to be secondary non responders to botulinum toxin treatment should be given a trial of EMG guided injections. In: MOVEMENT DISORDERS. (pp. S295 - S296). WILEY-LISS

Costa, DC; Lees, AJ; (2002) Dopamine neurotransmission, Parkinson's disease and SPET. EUR J NUCL MED , 29 (1) 163 - 163.

Cowan, DA; Russell, NJ; Mamais, A; Sheppard, DM; (2002) Antarctic Dry Valley mineral soils contain unexpectedly high levels of microbial biomass. EXTREMOPHILES , 6 (5) 431 - 436. 10.1007/s00792-002-002-0276-5.

D

Dale, RC; Church, AJ; Benton, S; Surtees, RA; Lees, A; Thompson, EJ; ... Neville, BG; + view all (2002) Post-streptococcal autoimmune dystonia with isolated bilateral striatal necrosis. DEV MED CHILD NEUROL , 44 (7) 485 - 489.

Dale, RC; Church, AJ; Surtees, RA; Lees, AJ; Neville, AG; Giovannoni, G; (2002) Re-emergence of encephalitis lethargica-like syndrome: Evidence of CNS autoimmunity. In: MOVEMENT DISORDERS. (pp. S260 - S260). WILEY-LISS

Dale, RC; Church, AJ; Surtees, RAH; Lees, AJ; Neville, BGR; Giovanni, G; (2002) Re-emergence of encephalitis lethargica: New evidence of an autoimmune CNS disease. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY , 73 (2) 214 - 214.

Davies, NP; Beesley, C; Elliott, PM; Holton, J; Lake, B; Landon, DN; ... Hanna, MG; + view all (2002) Intronic and missense mutations within the LAMP-2 gene in Danon disease (X linked vacuolar cardiomyopathy and myopathy). J NEUROL NEUROSUR PS , 72 (1) 139 - 139.

Davies, NP; Eunson, LH; Hanna, MG; (2002) Results of a United Kingdom-wide clinical and molecular genetic study of myotonia congenita. J NEUROL NEUROSUR PS , 72 (1) 137 - 137.

Davies, NP; Sutton, I; Winer, JB; Moorcroft, P; Hall, HS; Cole, T; ... Hanna, MG; + view all (2002) The sodium channel syndromes: Expanding the phenotype associated with SCN4A mutations. J NEUROL NEUROSUR PS , 73 (2) 229 - 229.

Davies, NP; Weber, A; Mueller, R; Hilton-Jones, D; Chinnery, PF; Hanna, MG; (2002) Andersen's syndrome: A skeletal muscle potassium channel disorder. In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. S54 - S54).

Davies, NP; Weber, A; Mueller, R; Hilton-Jones, D; Chinnery, PF; Hanna, MG; (2002) Periodic paralysis, malignant ventricular arrhythmia and dysmorphism (Andersen's syndrome): A skeletal muscle potassium channel disorder. J NEUROL NEUROSUR PS , 73 (2) 221 - 221.

de Carvalho, M; Houlden, H; (2002) Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutation. NEUROLOGY , 59 (11) 1823 - 1823.

De Carvalho, M; Houlden, H; Goizet, C; Lacombe, D; (2002) Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutation [4] (multiple letters). Neurology , 59 (11) 1823 - 1823.

de Silva, R; (2002) Functional aspects of alpha-synuclein. In: Neurodgenerative Disorders Associated with α-Synuclein Pathology. (1 - 10). Medicina stm Editores, S.L.: Barcelona.

de Silva, R; Farrer, M; (2002) Tau neurotoxicity without the lesions: a fly challenges a tangled web. TRENDS NEUROSCI , 25 (7) 327 - 329.

de Silva, R; Hardy, J; Crook, J; Khan, N; Graham, EA; Morris, CM; ... Lees, AJ; + view all (2002) The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease. NEUROSCI LETT , 330 (2) 201 - 203.

de Silva, R; Lashley, T; Gibb, G; Hanger, D; Revesz, T; Lees, A; (2002) Dissection of tau isoform composition of tauopathy lesions using novel isoform-specific monoclonal antibodies. In: MOVEMENT DISORDERS. (pp. S20 - S20). WILEY-LISS

de Silva, R; Lees, A; (2002) Genetics of the tau locus in progressive supranuclear palsy. In: MOVEMENT DISORDERS. (pp. 1405 - 1405). WILEY-LISS

Dobson-Stone, C; Danek, A; Rampoldi, L; Hardie, RJ; Chalmers, RM; Wood, NW; ... Monaco, AP; + view all (2002) Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis. EUR J HUM GENET , 10 (11) 773 - +. 10.1038/sj/ejhg.5200866.

Dominguez, DI; De Strooper, B; (2002) Novel therapeutic strategies provide the real test for the amyloid hypothesis of Alzheimer's disease. Trends Pharmacol Sci , 23 (7) 324 - 330.

E

Eapen, V; Lees, AJ; Lakke, JPWF; Trimble, MR; Robertson, MM; (2002) Adult-onset tic disorders. MOVEMENT DISORD , 17 (4) 735 - 740. 10.1002/mds.10180.

Eunson, L; Khan, NL; Quinn, N; Bhatia, K; Wood, NW; Davis, MB; (2002) Novel parkin mutations in early-onset parkinsonism. In: JOURNAL OF MEDICAL GENETICS. (pp. S71 - S71). BRITISH MED JOURNAL PUBL GROUP

Everett, CM; Saveliev, A; Webster, Z; Wood, NW; Festenstein, R; (2002) The molecular basis for aberrant gene regulation in Friedreich's ataxia. J NEUROL NEUROSUR PS , 73 (2) 225 - 225.

Evidente, VGH; Advincula, J; Esteban, R; Pasco, P; Alfon, JA; Natividad, FF; ... Singleton, A; + view all (2002) Phenomenology of "Lubag" or X-linked dystonia-parkinsonism. MOVEMENT DISORDERS , 17 (6) 1271 - 1277. 10.1002/mds.10271.

Evidente, VGH; Gwinn-Hardy, K; Hardy, J; Hernandez, D; Singleton, A; (2002) X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: A more benign phenotype? MOVEMENT DISORDERS , 17 (1) 200 - 202. 10.1002/mds.1263.

F

Farrer, M; Skipper, L; Berg, M; Bisceglio, G; Hanson, M; Hardy, J; ... Aasly, J; + view all (2002) The Tau H1 haplotype is associated with Parkinson's disease in the Norwegian population. NEUROSCIENCE LETTERS , 322 (2) , Article PII S0304-3940(02)00106-4. 10.1016/S0304-3940(02)00106-4.

Fenske, CD; Warner, TT; Patel, H; Patton, MA; Proukakis, C; Crosby, AH; (2002) Genetic heterogeneity in Silver syndrome. In: AMERICAN JOURNAL OF HUMAN GENETICS. (pp. 517 - 517). UNIV CHICAGO PRESS

Fidani, L; Compton, D; Hardy, J; Petersen, RC; Tangalos, E; Mirtsou, V; ... De Vrieze, FW; + view all (2002) No association between the lipoprotein lipase S447X polymorphism and Alzheimer's disease. NEUROSCI LETT , 322 (3) 192 - 194.

Fidani, L; Goulas, A; Mirtsou, V; Petersen, RC; Tangalos, E; Crook, R; Hardy, J; (2002) Interleukin-1A polymorphism is not associated with late onset Alzheimer's disease. NEUROSCIENCE LETTERS , 323 (1) , Article PII S0304-3940(02)00114-3. 10.1016/S0304-3940(02)00114-3.

Flood, DG; Reaume, AG; Dorfman, KS; Lin, YG; Lang, DM; Trusko, SP; ... Scott, RW; + view all (2002) FAD mutant PS-1 gene-targeted mice: increased A beta 42 and A beta deposition without APP overproduction. Neurobiol Aging , 23 (3) 335 - 348.

G

Gabriel, CM; Gregson, NA; Wood, NW; Hughes, RAC; (2002) Immunological study of hereditary motor and sensory neuropathy type 1 a (HMSN1 a). J NEUROL NEUROSUR PS , 72 (2) 230 - 235.

Garrard, P; Blake, J; Stinton, V; Hanna, M; Reilly, M; Holton, J; ... Honan, W; + view all (2002) Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA? Journal of Neurology, Neurosurgery and Psychiatry , 73 (2) pp.207 - 208.

Garrard, P; Blake, J; Stinton, V; Hanna, MG; Reilly, MM; Holton, JL; ... Honan, WP; + view all (2002) Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA? J NEUROL NEUROSUR PS , 73 (2) 207 - 208. Green open access
file

Gibb, G; Hanger, D; Anderton, B; Connell, J; Grierson, A; De Silva, R; Revesz, T; (2002) Comparision of tau protein expression in AD, FTDP-17, PSP and Pick's disease. NEUROBIOL AGING , 23 (1) S505 - S505.

Goldstein, DB; Ramachandran, V; Wood, N; Shorvon, S; (2002) Pharmacogenomics of neurological disorders. In: Pharmacogenomics: The search for Individualised Therapies.

Goudreau, JL; Maraganore, DM; Farrer, MJ; Lesnick, TG; Singleton, AB; Bower, JH; ... Rocca, WA; + view all (2002) Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease. MOVEMENT DISORDERS , 17 (6) 1305 - 1311. 10.1002/mds.10268.

Goulas, A; Fidani, L; Kotsis, A; Mirtsou, V; Petersen, RC; Tangalos, E; Hardy, J; (2002) An association study of a functional catalase gene polymorphism,-262C -> T, and patients with Alzheimer's disease. NEUROSCI LETT , 330 (2) 210 - 212.

Guillet, C; Lelievre, E; Plun-Favreau, H; Froger, J; Chabbert, M; Hermann, J; ... Elson, G; + view all (2002) Functionally active fusion protein of the novel composite cytokine CLC/soluble CNTF receptor. EUR J BIOCHEM , 269 (7) 1932 - 1941. 10.1046/j.1432-1033.2002.02850.x.

H

Hafezparast, M; Ahmad-Annuar, A; Wood, NW; Tabrizi, SJ; Fisher, EMC; (2002) Mouse models for neurological disease. LANCET NEUROL , 1 (4) 215 - 224.

Hanger, D; Gibb, G; Anderton, B; Ghiso, J; Rostagno, A; Frangione, B; ... Revesz, T; + view all (2002) Tau in familial Danish dementia brain is similar, but not identical, to that found in familial British dementia and PHF-tau in Alzheimer's disease. NEUROBIOL AGING , 23 (1) S505 - S505.

Hanger, DP; Gibb, GM; de Silva, R; Boutajangout, A; Brion, JP; Revesz, T; ... Anderton, BH; + view all (2002) The complex relationship between soluble and insoluble tau in tauopathies revealed by efficient dephosphorylation and specific antibodies. FEBS LETT , 531 (3) 538 - 542.

Hanna, MG; Wood, NW; (2002) Running a neurogenetic clinic. J NEUROL NEUROSUR PS , 73 2 - 4.

Hardy, J; (2002) Pathways to primary neurodegenerative disease. NEUROLOGIA , 17 (8) 399 - 401.

Hardy, J; (2002) Testing times for the "amyloid cascade hypothesis". NEUROBIOLOGY OF AGING , 23 (6) , Article PII S0197-4580(02)00042-8. 10.1016/S0197-4580(02)00042-8.

Hardy, J; (2002) The real problem in association studies. AMERICAN JOURNAL OF MEDICAL GENETICS , 114 (2) 253 - 253. 10.1002/ajmg.10294.

Hardy, J; Selkoe, DJ; (2002) Medicine - The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeutics. SCIENCE , 297 (5580) 353 - 356. 10.1126/science.1072994.

Hartmann, D; de Strooper, B; Serneels, L; Craessaerts, K; Herreman, A; Annaert, W; ... Saftig, P; + view all (2002) The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts. Hum Mol Genet , 11 (21) 2615 - 2624.

Hawthorne, M; (2002) Botulinum toxins in the treatment of laryngeal and oromandibular dystonia. In: OPTIMAL PATIENT MANAGEMENT WITH BOTULINUM TOXINS: EVIDENCE AND EXPERIENCE. (pp. 40 - 46).

Henderson, JN; Crook, R; Crook, J; Hardy, J; Onstead, L; Carson-Henderson, L; ... Williams, B; + view all (2002) Apolipoprotein E4 and tau allele frequencies among Choctaw Indians. NEUROSCIENCE LETTERS , 324 (1) , Article PII S0304-3940(02)00150-7. 10.1016/S0304-3940(02)00150-7.

Holton, J; Lashley, T; Revesz, T; Rostagno, A; Frangione, B; Ghiso, J; (2002) Morphological evidence of the activation of the classical complement pathway in the BRI gene-related dementias. NEUROBIOL AGING , 23 (1) S205 - S206.

Holton, J.L.; Lashley, T.; Ghiso, J.; Braendgaard, H.; Vidal, R.; Guerin, C.; ... Revesz, T.; + view all (2002) Familial Danish dementia: a novel form of cerebral amyloidosis associated with deposition of both amyloid-Dan and amyloid-beta. Journal of Neuropathology and Experimental Neurology , 61 (3) pp. 254-267.

Holton, JL; Lashley, T; Ghiso, J; Braendgaard, H; Vidal, R; Guerin, CJ; ... Revesz, T; + view all (2002) Familial Danish dementia: A novel form of cerebral amyloidosis associated with deposition of both amyloid-Dan and amyloid-beta. J NEUROPATH EXP NEUR , 61 (3) 254 - 267.

Holton, JL; Revesz, T; Crooks, R; Scaravilli, F; (2002) Evidence for pathological involvement of the spinal cord in motor neuron disease-inclusion dementia. ACTA NEUROPATHOL , 103 (3) 221 - 227. 10.1007/s004010100457.

Houlden, H; Roper, H; Willis, T; Schenone, A; Di Battista, C; Wood, NW; Reilly, M; (2002) Giant axonal neuropathy is caused by mutations in the gigaxonin gene: Clinical, genetic, and pathological characterisation of three families. J NEUROL NEUROSUR PS , 73 (2) 225 - 225.

Houlden, H; Smith, S; de Carvalho, M; Blake, J; Mathias, C; Wood, NW; Reilly, MM; (2002) Clinical and genetic characterization of families with triple A (Allgrove) syndrome. BRAIN , 125 2681 - 2690.

Houlden, H; Smith, S; de Carvalho, M; Mathias, C; Blake, J; Wood, NW; Reilly, M; (2002) Clinical and genetic characterisation of families with triple a (Allgrove) syndrome. J NEUROL NEUROSUR PS , 73 (2) 225 - 225.

Houlden, H.; Smith, S.; de Carvalho, M.; Blake, J.; Mathias, C.; Wood, N.W.; Reilly, M.M.; (2002) Clinical and genetic characterization of families with triple A (Allgrove) syndrome. Brain , 125 (12) pp. 2681-2690. 10.1093/brain/awf270.

Hughes, AJ; Daniel, SE; Ben-Shlomo, Y; Lees, AJ; (2002) The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service. Brain , 125 (Pt 4) 861 - 870.

Hughes, AJ; Lees, AJ; (2002) The evolution of the acute response to L-dopa in Parkinson's disease. In: MOVEMENT DISORDERS. (pp. S97 - S98).

Hyman, N; (2002) Botulinum toxins in the treatment of cervical dystonia. In: OPTIMAL PATIENT MANAGEMENT WITH BOTULINUM TOXINS: EVIDENCE AND EXPERIENCE. (pp. 10 - 15).

I

Isenberg, DA; Allen, E; Farewell, V; Ehrenstein, MR; Cooper, R; Hanna, M; ... Miller, F; + view all (2002) Development of disease activity and damage indices for myositis: Further testing of four tools in adult onset patients. In: ARTHRITIS AND RHEUMATISM. (pp. S488 - S488). WILEY-LISS

Isotalo, PA; Donnelly, JG; Zetterberg, H; Rymo, L; Coppola, A; D'Angelo, A; ... Blennow, K; + view all (2002) Comment on 'increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos' (multiple letters) [2]. European Journal of Human Genetics , 10 (10) 578 - 582. 10.1038/sj.ejhg.5200862.

J

Jacques, TS; Holton, J; Watts, PM; Wills, AJ; Smith, SE; Hanna, MG; (2002) Tubular agaregate myopathy with abnormal pupils and skeletal deformities. J NEUROL NEUROSUR PS , 73 (3) 324 - 326.

Janssen, JC; Beck, JA; Campbell, TA; Dickinson, A; Fox, NC; Harvey, RJ; ... Collinge, J; + view all (2002) Early onset familial alzheimer's disease: Mutation frequency in 31 families. J NEUROL NEUROSUR PS , 73 (2) 219 - 219.

Janssen, JC; Fox, NC; Harvey, RJ; Houlden, H; Rossor, MN; Beck, JA; ... Collinge, J; + view all (2002) Early-onset familial Alzheimer's disease: Mutation frequency in 31 families. NEUROBIOL AGING , 23 (1) S311 - S311.

Janssen, JC; Warrington, EK; Morris, HR; Lantos, P; Brown, J; Revesz, T; ... Rossor, MN; + view all (2002) Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation. NEUROLOGY , 58 (8) 1161 - 1168.

Jarman, PR; Wood, NW; (2002) Genetics of movement disorders and ataxia. Journal of Neurology, Neurosurgery and Psychiatry , 73 (Suppl.2) II22 - II26.

Jarman, PR; Wood, NW; (2002) Genetics of movement disorders and ataxia. J NEUROL NEUROSUR PS , 73 22 - 26.

Jeffery, S; Wilkinson, P; Warner, TT; Crosby, AH; (2002) Confirmation and refinement of the SPG5A locus for pure autosomal recessive hereditary spastic paraplegia. In: AMERICAN JOURNAL OF HUMAN GENETICS. (pp. 433 - 433). UNIV CHICAGO PRESS

K

Kang, DE; Soriano, S; Xia, X; Eberhart, CG; De Strooper, B; Zheng, H; Koo, EH; (2002) Presenilin couples the paired phosphorylation of beta-catenin independent of axin: implications for beta-catenin activation in tumorigenesis. Cell , 110 (6) 751 - 762.

Katzenschlager, R; Costa, D; Gacinovic, S; Lees, AJ; (2002) [I-123]-FP-CIT-SPECT in the early diagnosis of PD presenting as exercise-induced dystonia. NEUROLOGY , 59 (12) 1974 - 1976.

Katzenschlager, R; Costa, D; Gerschlager, W; O'Sullivan, JD; Lees, AJ; Brown, P; (2002) Dopamine transporter imaging with I-123-FP-CIT SPECT demonstrates marked presynaptic nigrostriatal dopaminergic deficit in orthostatic tremor. In: MOVEMENT DISORDERS. (pp. S346 - S346).

Katzenschlager, R; Lees, AJ; (2002) Treatment of Parkinson's disease: levodopa as the first choice. J Neurol , 249 Suppl 2 II19 - II24. 10.1007/s00415-002-1204-4.

Khan, N; Valente, EM; Brooks, DJ; Piccini, P; Bhatia, KP; Quinn, NP; Wood, NW; (2002) The genetic basis and phenotypic variability in early onset parkinsonism. J NEUROL NEUROSUR PS , 73 (2) 213 - 213.

Khan, NL; Brooks, DJ; Pavese, N; Sweeney, MG; Wood, NW; Lees, AJ; Piccini, P; (2002) Progression of nigrostriatal dysfunction in a parkin kindred: an [F-18] dopa PET and clinical study. BRAIN , 125 2248 - 2256.

Khan, NL; Brooks, DJ; Pavese, N; Wood, NW; Lees, AJ; Piccini, P; (2002) Progression of nigrostriatal dysfunction in a parkin kindred: An F-18-dopa PET and clinical study. J NEUROL NEUROSUR PS , 72 (1) 134 - 134.

Khan, NL; Valente, EM; Bentivoglio, AR; Wood, NW; Albanese, A; Brooks, DJ; Piccini, P; (2002) Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: An F-18-dopa PET study. ANN NEUROL , 52 (6) 849 - 853. 10.1002/ana.10417.

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Utton, M; Connell, J; Asuni, A; Miller, C; Anderton, B; van Slegtenhorst, M; ... Lees, A; + view all (2002) The mechanism of slow axonal transport of the microtubule-associated protein tau and the transport rates of different isoforms and mutants. NEUROBIOL AGING , 23 (1) S499 - S499.

Utton, MA; Connell, J; Asuni, AA; van Slegtenhorst, M; Hutton, M; de Silva, R; ... Anderton, BH; + view all (2002) The slow axonal transport of the microtubule-associated protein tau and the transport rates of different Isoforms and mutants in cultured neurons. J NEUROSCI , 22 (15) 6394 - 6400.

V

Valente, EM; Brancati, F; Caputo, V; Graham, EA; Davis, MB; Ferraris, A; ... European Consortium Genetic Suscep,; + view all (2002) PARK6 is a common cause of familial parkinsonism. NEUROLOGICAL SCIENCES , 23 S117 - S118.

Valente, EM; Brancati, F; Ferraris, A; Graham, EA; Davis, MB; Breteler, MMB; ... European Consortium Genetic Suscep,; + view all (2002) PARK6-linked parkinsonism occurs in several European families. ANN NEUROL , 51 (1) 14 - 18. 10.1002/ana.10053.

Valente, EM; Misbahuddin, A; Brancati, F; Placzek, MR; Dallapiccola, B; Warner, TT; (2002) Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclomasdystonia: Evidence for genetic heterogeneity. In: MOVEMENT DISORDERS. (pp. S331 - S331). WILEY-LISS

van den Maagdenberg, AMJM; Terwindt, GM; Kors, EE; Imbrici, P; Giffin, NJ; Sherrington, CR; ... Frants, RR; + view all (2002) Two novel mutations in the CACNA1A gene leading to identical functional consequences but with different phenotypic expression. In: AMERICAN JOURNAL OF HUMAN GENETICS. (pp. 520 - 520). UNIV CHICAGO PRESS

Vaughan, JR; Revesz, T; Petrucelli, L; Luecking, C; Farrer, M; Lees, AJ; (2002) Prominent neurolibrillary tangle pathology in a Parkin brain. In: MOVEMENT DISORDERS. (pp. S156 - S156). WILEY-LISS

Visvikis, D; Gacinovic, S; Erlandsson, K; Katzenschlager, R; O'Sullivan, JD; Lees, AJ; Costa, DC; (2002) Analysis of 123I-FPCIT 9DaTSCANTM) binding in normal volunteers and Parkinson's disease. In: Nuclear Medicine Communications. (pp. 378 - 379).

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W

Walker, RH; Friedman, J; Wiener, J; Hobler, R; Gwinn-Hardy, K; Adam, A; ... Hardy, J; + view all (2002) A family with a tau P301L mutation presenting with parkinsonism. PARKINSONISM & RELATED DISORDERS , 9 (2) , Article PII S1353-8020(02)00003-2. 10.1016/S1353-8020(02)00003-2.

Ward, KN; White, RP; Mackinnon, S; Hanna, M; (2002) Human herpesvirus-7 infection of the CNS with acute myelitis in an adult bone marrow recipient. BONE MARROW TRANSPL , 30 (12) 983 - 985. 10.1038/sj.bmt.1703774.

Warren, JD; Mummery, CJ; Al-Din, AS; Brown, P; Wood, NW; (2002) Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look-alike? MOVEMENT DISORD , 17 (3) 563 - 567. 10.1002/mds.10122.

West, A; Periquet, M; Lincoln, S; Lucking, CB; Nicholl, D; Bonifati, V; ... European Consortium Genetic Suscep,; + view all (2002) Complex relationship between parkin mutations and Parkinson disease. AM J MED GENET , 114 (5) 584 - 591. 10.1002/ajmg.10525.

West, AB; Maraganore, D; Crook, J; Lesnick, T; Lockhart, PJ; Wilkes, KM; ... Farrer, MJ; + view all (2002) Functional association of the parkin gene promoter with idiopathic Parkinson's disease. HUMAN MOLECULAR GENETICS , 11 (22) 2787 - 2792. 10.1093/hmg/11.22.2787.

Wu, RM; Shan, DE; Sun, CM; Liu, RS; Hwu, WL; Tai, CH; ... Lincoln, S; + view all (2002) Clinical, F-18-dopa PET, and genetic analysis of an ethnic chinese kindred with early-onset parkinsonism and parkin gene mutations. MOVEMENT DISORDERS , 17 (4) 670 - 675. 10.1002/mds.10184.

Z

Zermansky, AJ; Ben-Shlomo, Y; Thomson, R; Lees, AJ; Burn, DJ; (2002) Anxiety and depression in PSP: Common, but unrelated to disease severity. In: MOVEMENT DISORDERS. (pp. S247 - S247).

Zetterberg, H; Coppola, A; D'Angelo, A; Palmér, M; Rymo, L; Blennow, K; (2002) No association between the MTHFR A1298C and transcobalamin C776G genetic polymorphisms and hyperhomocysteinemia in thrombotic disease. Thromb Res , 108 (2-3) 127 - 131.

Zetterberg, H; Jansson, A; Rymo, L; Chen, F; Karlsson, A; Klein, G; Brodin, B; (2002) The Epstein-Barr virus ZEBRA protein activates transcription from the early lytic F promoter by binding to a promoter-proximal AP-1-like site. Journal of General Virology , 83 (8) 2007 - 2014.

Zetterberg, H; Jansson, A; Rymo, L; Chen, F; Karlsson, A; Klein, G; Brodin, B; (2002) The Epstein-Barr virus ZEBRA protein activates transcription from the early lytic F promoter by binding to a promoter-proximal AP-1-like site. J Gen Virol , 83 (Pt 8) 2007 - 2014.

Zetterberg, H; Palmér, M; Ricksten, A; Poirier, J; Palmqvist, L; Rymo, L; ... Blennow, K; + view all (2002) Influence of the apolipoprotein E epsilon4 allele on human embryonic development. Neurosci Lett , 324 (3) 189 - 192.

Zetterberg, H; Regland, B; Palmér, M; Ricksten, A; Palmqvist, L; Rymo, L; ... Blennow, K; + view all (2002) Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos. Eur J Hum Genet , 10 (2) 113 - 118. 10.1038/sj.ejhg.5200767.

Zetterberg, H; Regland, B; Palmér, M; Rymo, L; Zafiropoulos, A; Arvanitis, DA; ... Blennow, K; + view all (2002) The transcobalamin codon 259 polymorphism influences the risk of human spontaneous abortion. Hum Reprod , 17 (12) 3033 - 3036.

Zijlmans, J; Booij, J; Valk, J; Lees, A; Horstink, M; (2002) Posttraumatic tremor without parkinsonism in a patient with complete contralateral loss of the nigrostriatal pathway. MOVEMENT DISORD , 17 (5) 1086 - 1088. 10.1002/mds.10203.

Zijlmans, J; Daniel, S; Lees, A; (2002) Clinical features of patients with pathology confirmed vascular parkinsonism. In: MOVEMENT DISORDERS. (pp. S248 - S249).

This list was generated on Sun Aug 31 04:02:41 2014 BST.