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Number of items: 158.
A
| Adlkofer, F and Aguzzi, A and Baumeister, R and Haass, C and Silva, ODE and DeStrooper, B and Dotti, C and Efthimiopoulos, S and Gomez-Isla, T and Growdon, J and Hardy, J and Hock, C and Nitsch, R and Lannfelt, L and Pohlner, J and Rossor, M and Tovar, K and Unsicker, K and Wiltfang, J (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 and Ames, PRJ and Donohue, S and Stanyer, L and Noorouz-Zadeh, J and Ravirajan, C and 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 and Lewis, PA and Piper, S and Crook, R and Baker, M and Findlay, K and Singleton, A and Hogg, M and Younkin, L and Younkin, SG and Hardy, J and Hutton, M and Boeve, BF and Tang-Wai, D and Golde, TE (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 and Groves, M and Martinian, L and Kuo, LT and 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 and Bushby, KMD and Hanna, MG and Muntoni, FN and Hilton-Jones, D and Newsom-Davis, J (2002) Diagnosing rare neuromuscular diseases - The jump from research to service. In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. S72 - S72). |
| Asmus, F and Zimprich, A and du Montcel, ST and Kabus, C and Deuschl, G and Kupsch, A and Ziemann, U and Castro, M and Kuhn, AA and Strom, TM and Vidailhet, M and Bhatia, KP and Durr, A and Wood, NW and Brice, A and Gasser, T (2002) Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype. ANN NEUROL , 52 (4) 489 - 492. 10.1002/ana.10325. |
B
| Bajaj, NPS and Waldman, A and Orrell, R and Wood, NW and 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 and Wood, NW (2002) Dopa-responsive dystonia -- the story so far. Neuropediatrics , 33 (1) 1 - 5. |
| Ben-Shlomo, Y and Camfield, L and Warner, T and 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. |
| Boeve, BF and Maraganore, DM and Parisi, JE and Ivnik, RJ and Westmoreland, BF and Dickson, DW and Hutton, M and Hardy, J and Caselli, RJ and Petersen, RC (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. and Brand, M. and Hargreaves, I. and Heales, S. and Land, J. and Smolenski, R. and Davies, N.A. and Cooper, C.E. and Singer, M. (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. |
C
| Camfield, L and Ben-Shlomo, Y and Warner, TT and Epidemiological Study Dystonia Eur, (2002) Impact of cervical dystonia on quality of life. MOVEMENT DISORD , 17 (4) 838 - 841. 10.1002/mds.10127. |
| Caselli, RJ and Hentz, JG and Osborne, D and Graff-Radford, NR and Barbieri, CJ and Alexander, GE and Hall, GR and Reiman, EM and Hardy, J and Saunders, AM (2002) Apolipoprotein E and intellectual achievement. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY , 50 (1) 49 - 54. 10.1046/j.1532-5415.2002.50007.x. |
| Chan, D and Revesz, T and Rudge, P (2002) Hippocampal, but not parahippocampal, damage in a case of dense retrograde amnesia: a pathological study. NEUROSCI LETT , 329 (1) 61 - 64. |
| Chinnery, PF and Walls, TJ and Hanna, MG and Bates, D and Fawcett, PRW (2002) Normokalemic periodic paralysis revisited: Does it exist? ANN NEUROL , 52 (2) 251 - 252. 10.1002/ana.10257. |
| Chong, MS and Smith, TE and 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. |
| Compton, D and DeVrieze, FW and Petersen, RC and Tangalos, E and Li, L and 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. |
| Cowan, DA and Russell, NJ and Mamais, A and 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
| Davies, NP and Beesley, C and Elliott, PM and Holton, J and Lake, B and Landon, DN and Lee, P and Mundy, H and Winchester, B and Hanna, MG (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 and Eunson, LH and 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 and Sutton, I and Winer, JB and Moorcroft, P and Hall, HS and Cole, T and Davies, MB and Valente, EM and Brancati, F and Hammons, SR and Hanna, MG (2002) The sodium channel syndromes: Expanding the phenotype associated with SCN4A mutations. J NEUROL NEUROSUR PS , 73 (2) 229 - 229. |
| Davies, NP and Weber, A and Mueller, R and Hilton-Jones, D and Chinnery, PF and Hanna, MG (2002) Andersen's syndrome: A skeletal muscle potassium channel disorder. In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. S54 - S54). |
| Davies, NP and Weber, A and Mueller, R and Hilton-Jones, D and Chinnery, PF and 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 and Houlden, H (2002) Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutation. 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 and Farrer, M (2002) Tau neurotoxicity without the lesions: a fly challenges a tangled web. TRENDS NEUROSCI , 25 (7) 327 - 329. |
| de Silva, R and Hardy, J and Crook, J and Khan, N and Graham, EA and Morris, CM and Wood, NW and Lees, AJ (2002) The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease. NEUROSCI LETT , 330 (2) 201 - 203. |
| de Silva, R and Lashley, T and Gibb, G and Hanger, D and Revesz, T and 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 and Lees, A (2002) Genetics of the tau locus in progressive supranuclear palsy. In: MOVEMENT DISORDERS. (pp. 1405 - 1405). WILEY-LISS |
| Djamshidian, A and Grassl, R and Seltenhammer, M and Czech, T and Baumgartner, C and Schmidbauer, M and Ulrich, W and Zimprich, F (2002) Altered expression of voltage-dependent calcium channel alpha(1) subunits in temporal lobe epilepsy with Ammon's horn sclerosis. NEUROSCIENCE , 111 (1) 57 - 69. |
| Dobson-Stone, C and Danek, A and Rampoldi, L and Hardie, RJ and Chalmers, RM and Wood, NW and Bohlega, S and Dotti, MT and Federico, A and Shizuka, M and Tanaka, M and Watanabe, M and Ikeda, Y and Brin, M and Goldfarb, LG and Karp, BI and Mohiddin, S and Fananapazir, L and Storch, A and Fryer, AE and Maddison, P and Sibon, I and Trevisol-Bittencourt, PC and Singer, C and Caballero, IR and Aasly, JO and Schmierer, K and Dengler, R and Hiersemenzel, LP and Zeviani, M and Meiner, V and Lossos, A and Johnson, S and Mercado, FC and Sorrentino, G and Dupre, N and Rouleau, GA and Volkmann, J and Arpa, J and Lees, A and Geraud, G and Chouinard, S and Nemeth, A and Monaco, AP (2002) Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis. EUR J HUM GENET , 10 (11) 773 - +. 10.1038/sj/ejhg.5200866. |
E
| Eunson, L and Khan, NL and Quinn, N and Bhatia, K and Wood, NW and 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 and Saveliev, A and Webster, Z and Wood, NW and Festenstein, R (2002) The molecular basis for aberrant gene regulation in Friedreich's ataxia. J NEUROL NEUROSUR PS , 73 (2) 225 - 225. |
| Evidente, VGH and Advincula, J and Esteban, R and Pasco, P and Alfon, JA and Natividad, FF and Cuanang, J and San Luis, A and Gwinn-Hardy, K and Hardy, J and Hernandez, D and Singleton, A (2002) Phenomenology of "Lubag" or X-linked dystonia-parkinsonism. MOVEMENT DISORDERS , 17 (6) 1271 - 1277. 10.1002/mds.10271. |
| Evidente, VGH and Gwinn-Hardy, K and Hardy, J and Hernandez, D and 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 and Skipper, L and Berg, M and Bisceglio, G and Hanson, M and Hardy, J and Adam, A and Gwinn-Hardy, K and Aasly, J (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 and Warner, TT and Patel, H and Patton, MA and Proukakis, C and Crosby, AH (2002) Genetic heterogeneity in Silver syndrome. In: AMERICAN JOURNAL OF HUMAN GENETICS. (pp. 517 - 517). UNIV CHICAGO PRESS |
| Fidani, L and Compton, D and Hardy, J and Petersen, RC and Tangalos, E and Mirtsou, V and Goulas, A and De Vrieze, FW (2002) No association between the lipoprotein lipase S447X polymorphism and Alzheimer's disease. NEUROSCI LETT , 322 (3) 192 - 194. |
| Fidani, L and Goulas, A and Mirtsou, V and Petersen, RC and Tangalos, E and Crook, R and 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. |
G
| Gabriel, CM and Gregson, NA and Wood, NW and 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 and Blake, J and Stinton, V and Hanna, M and Reilly, M and Holton, J and Landon, D and Honan, W (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 and Blake, J and Stinton, V and Hanna, MG and Reilly, MM and Holton, JL and Landon, DN and Honan, WP (2002) Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA? J NEUROL NEUROSUR PS , 73 (2) 207 - 208. |  |
| Gibb, G and Hanger, D and Anderton, B and Connell, J and Grierson, A and De Silva, R and Revesz, T (2002) Comparision of tau protein expression in AD, FTDP-17, PSP and Pick's disease. NEUROBIOL AGING , 23 (1) S505 - S505. |
| Gnanalingham, KK and Chakraborty, A and Galloway, M and Revesz, T and Powell, M (2002) Osteosarcoma and fibrosarcoma caused by postoperative radiotherapy for a pituitary adenoma. J NEUROSURG , 96 (5) 960 - 963. |
| Goetz, P and Lafuente, J and Revesz, T and Galloway, M and Dogan, A and Kitchen, N (2002) Primary low-grade B-cell lymphoma of mucosa-associated lymphoid tissue of the dura mimicking the presentation of an acute subdural hematoma - Case report and review of the literature. J NEUROSURG , 96 (3) 611 - 614. |
| Goldstein, DB and Ramachandran, V and Wood, N and Shorvon, S (2002) Pharmacogenomics of neurological disorders. In: Pharmacogenomics: The search for Individualised Therapies. |
| Goudreau, JL and Maraganore, DM and Farrer, MJ and Lesnick, TG and Singleton, AB and Bower, JH and Hardy, JA and Rocca, WA (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 and Fidani, L and Kotsis, A and Mirtsou, V and Petersen, RC and Tangalos, E and 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. |
| Graf, D and Nethisinghe, S and Palmer, DB and Fisher, AG and Merkenschlager, M (2002) The developmentally regulated expression of Twisted gastrulation reveals a role for bone morphogenetic proteins in the control of T cell development. J EXP MED , 196 (2) 163 - 171. 10.1084/jem.20020276. |
| Guillet, C and Lelievre, E and Plun-Favreau, H and Froger, J and Chabbert, M and Hermann, J and de Coignac, AB and Bonnefoy, JY and Gascan, H and Gauchat, JF and Elson, G (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 and Ahmad-Annuar, A and Wood, NW and Tabrizi, SJ and Fisher, EMC (2002) Mouse models for neurological disease. LANCET NEUROL , 1 (4) 215 - 224. |
| Hanger, D and Gibb, G and Anderton, B and Ghiso, J and Rostagno, A and Frangione, B and Holton, J and Revesz, T (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 and Gibb, GM and de Silva, R and Boutajangout, A and Brion, JP and Revesz, T and Lees, AJ and Anderton, BH (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 and 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 and 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. |
| Henderson, JN and Crook, R and Crook, J and Hardy, J and Onstead, L and Carson-Henderson, L and Mayer, P and Parker, B and Petersen, R and Williams, B (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 and Lashley, T and Revesz, T and Rostagno, A and Frangione, B and 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. and Lashley, T. and Ghiso, J. and Braendgaard, H. and Vidal, R. and Guerin, C. and Gibb, G. and Hanger, D.P. and Rostango, A. and Anderton, B. and Strand, C. and Ayling, H. and Plant, G. and Frangione, B. and Bojsen-Moller, M. and Revesz, T. (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 and Lashley, T and Ghiso, J and Braendgaard, H and Vidal, R and Guerin, CJ and Gibb, G and Hanger, DP and Rostagno, A and Anderton, BH and Strand, C and Ayling, H and Plant, G and Frangione, B and Bojsen-Moller, M and Revesz, T (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 and Revesz, T and Crooks, R and 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 and Roper, H and Willis, T and Schenone, A and Di Battista, C and Wood, NW and 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 and Smith, S and de Carvalho, M and Blake, J and Mathias, C and Wood, NW and Reilly, MM (2002) Clinical and genetic characterization of families with triple A (Allgrove) syndrome. BRAIN , 125 2681 - 2690. |
| Houlden, H and Smith, S and de Carvalho, M and Mathias, C and Blake, J and Wood, NW and Reilly, M (2002) Clinical and genetic characterisation of families with triple a (Allgrove) syndrome. J NEUROL NEUROSUR PS , 73 (2) 225 - 225. |
| Houlden, H. and Smith, S. and de Carvalho, M. and Blake, J. and Mathias, C. and Wood, N.W. and 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. |
I
| Isenberg, DA and Allen, E and Farewell, V and Ehrenstein, MR and Cooper, R and Hanna, M and Lundberg, I and Oddis, C and Plotz, P and Vencovsky, J and Rider, L and Miller, F (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 |
J
| Jacques, TS and Holton, J and Watts, PM and Wills, AJ and Smith, SE and Hanna, MG (2002) Tubular agaregate myopathy with abnormal pupils and skeletal deformities. J NEUROL NEUROSUR PS , 73 (3) 324 - 326. |
| Janssen, JC and Beck, JA and Campbell, TA and Dickinson, A and Fox, NC and Harvey, RJ and Houlden, H and Rosser, MN and Collinge, J (2002) Early onset familial alzheimer's disease: Mutation frequency in 31 families. J NEUROL NEUROSUR PS , 73 (2) 219 - 219. |
| Janssen, JC and Fox, NC and Harvey, RJ and Houlden, H and Rossor, MN and Beck, JA and Campbell, TA and Dickinson, A and Collinge, J (2002) Early-onset familial Alzheimer's disease: Mutation frequency in 31 families. NEUROBIOL AGING , 23 (1) S311 - S311. |
| Janssen, JC and Warrington, EK and Morris, HR and Lantos, P and Brown, J and Revesz, T and Wood, N and Khan, MN and Cipolotti, L and Fox, NC and Rossor, MN (2002) Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation. NEUROLOGY , 58 (8) 1161 - 1168. |
| Jarman, PR and Wood, NW (2002) Genetics of movement disorders and ataxia. Journal of Neurology, Neurosurgery and Psychiatry , 73 (Suppl.2) II22 - II26. |
| Jarman, PR and Wood, NW (2002) Genetics of movement disorders and ataxia. J NEUROL NEUROSUR PS , 73 22 - 26. |
| Jeffery, S and Wilkinson, P and Warner, TT and 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
| Khan, N and Valente, EM and Brooks, DJ and Piccini, P and Bhatia, KP and Quinn, NP and Wood, NW (2002) The genetic basis and phenotypic variability in early onset parkinsonism. J NEUROL NEUROSUR PS , 73 (2) 213 - 213. |
| Khan, NL and Brooks, DJ and Pavese, N and Sweeney, MG and Wood, NW and Lees, AJ and 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 and Brooks, DJ and Pavese, N and Wood, NW and Lees, AJ and 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 and Valente, EM and Bentivoglio, AR and Wood, NW and Albanese, A and Brooks, DJ and 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. |
| Kinton, L and Johnson, MR and Smith, SJM and Farrell, F and Stevens, J and Rance, JB and Claudino, AM and Duncan, JS and Davis, MB and Wood, NW and Sander, JWA (2002) Partial epilepsy with pericentral spikes: A new familial epilepsy syndrome with evidence for linkage to chromosome 4p15. ANN NEUROL , 51 (6) 740 - 749. 10.1002/ana.10221. |
| Konkiewitz, EC and Trender-Gerhard, I and Kamm, C and Warner, T and Ben-Shlomo, Y and Gasser, T and Conrad, B and Ceballos-Baumann, AO (2002) Service-based survey of dystonia in Munich. NEUROEPIDEMIOLOGY , 21 (4) 202 - 206. |
| Kullmann, DM and Hanna, MG (2002) Neurological disorders caused by inherited ion-channel mutations. LANCET NEUROL , 1 (3) 157 - 166. |
L
| Lambert, JC and Araria-Goumidi, L and Myllykangas, L and Ellis, C and Wang, JC and Bullido, MJ and Harris, JM and Artiga, MJ and Hernandez, D and Kwon, JM and Frigard, B and Petersen, RC and Cumming, AM and Pasquier, F and Sastre, I and Tienari, PJ and Frank, A and Sulkava, R and Morris, JC and St Clair, D and Mann, DM and Wavrant-DeVrieze, F and Ezquerra-Trabalon, M and Amouyel, P and Hardy, J and Haltia, M and Valdivieso, F and Goate, AM and Perez-Tur, J and Lendon, CL and Chartier-Harlin, MC (2002) Contribution of APOE promoter polymorphisms to Alzheimer's disease risk. NEUROLOGY , 59 (1) 59 - 66. |
| Lantos, PL and Cairns, NJ and Khan, MN and King, A and Revesz, T and Janssen, JC and Morris, H and Rossor, MN (2002) Neuropathologic variation in frontotemporal dementia due to the intronic tau 10(+16) mutation. NEUROLOGY , 58 (8) 1169 - 1175. |
| Lee, MJ and Huang, YC and Sweeney, MG and Wood, NW and Reilly, MM and Yip, PK (2002) Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis. J NEUROL , 249 (9) 1311 - 1312. 10.1007/s00415-002-0762-9. |
| Lee, MJ and Nelson, I and Houlden, H and Sweeney, MG and Hilton-Jones, D and Blake, J and Wood, NW and Reilly, MM (2002) Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease. J NEUROL NEUROSUR PS , 73 (3) 304 - 306. |
| Leong, W and Cordivari, C and Houlden, H and Murray, N and Reilly, M (2002) Point mutations in PMP22 are rare causes of hereditary neuropathy with liability to pressure palsies. In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. S90 - S91). ELSEVIER SCIENCE BV |
| Liolitsa, D and Hanna, MG (2002) Models of mitochondrial disease. INT REV NEUROBIOL , 53 429 - 466. |
| Lisbonne, M and Plun-Favreau, H (2002) French Society of Immunology: Cytokine Meeting May 16-17, 2002, Le Croisic, Port-aux-Rocs, France. Eur Cytokine Netw , 13 (4) 474 - 476. |
| Littleton, ET and Man, WD and Holton, JL and Landon, DN and Hanna, MG and Polkey, MI and Taylor, GP (2002) Human T cell leukaemia virus type I associated neuromuscular disease causing respiratory failure. J NEUROL NEUROSUR PS , 72 (5) 650 - 652. |
| Lockhart, PJ and Holtom, B and Lincoln, S and Hussey, J and Zimprich, A and Gasser, T and Wszolek, ZK and Hardy, J and Farrer, MJ (2002) The human sideroflexin 5 (SFXN5) gene: sequence, expression analysis and exclusion as a candidate for PARK3. GENE , 285 (1-2) , Article PII S0378-1119(02)00402-X. 10.1016/S0378-1119(02)00402-X. |
| Lovestone, S and Hardy, J (2002) Psychotic genes or forgetful ones? NEUROLOGY , 59 (1) 11 - 12. |
M
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