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Number of items: 154.

A

Abou-Sleiman, PM and Healy, DG and Wood, NW (2004) Causes of Parkinson's disease: genetics of DJ-1. CELL TISSUE RES , 318 (1) 185 - 188. 10.1007/s00441-004-0922-6.

Abou-Sleiman, PM and Healy, DG and Wood, NW (2004) Genetic approaches to solving common diseases. J NEUROL , 251 (10) 1169 - 1172. 10.1007/s00415-004-0518-9.

Abramov, AY and Canevari, L and Duchen, MR (2004) Amyloid beta peptides induce mitochondrial dysfunction and oxidative stress in astrocytes and death of neurons through activation of NADPH oxidase. In: BIOPHYSICAL JOURNAL. (pp. 469A - 469A). BIOPHYSICAL SOCIETY

Abramov, AY and Canevari, L and Duchen, MR (2004) beta-amyloid peptides induce mitochondrial dysfunction and oxidative stress in astrocytes and death of neurons through activation of NADPH oxidase. J NEUROSCI , 24 (2) 565 - 575. 10.1523/JNEUROSCI.4042-03.2004.

Abramov, AY and Canevari, L and Duchen, MR (2004) Calcium signals induced by amylold beta peptide and their consequences in neurons and astrocytes in culture. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH , 1742 (1-3) 81 - 87. 10.1016/j.bbamcr.2004.09.006.

Ahluwalia, J and Tinker, A and Clapp, LH and Duchen, MR and Abramov, AY and Pope, S and Nobles, M and Segal, AW (2004) The large-conductance Ca2+-activated K+ channel is essential for innate immunity (Retracted article. See vol. 468, 2010). NATURE , 427 (6977) 853 - 858. 10.1038/nature02356.

Ansorge, O and Giunti, P and Michalik, A and Van Broeckhoven, C and Harding, B and Wood, N and Scaravilli, F (2004) Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats. ANN NEUROL , 56 (3) 448 - 452.

B

Bandopadhyay, R and Kingsbury, AE and Cookson, MR and Reid, AR and Evans, IM and Hope, AD and Pittman, AM and Lashley, T and Canet-Aviles, R and Miller, DW and McLendon, C and Strand, C and Leonard, AJ and Abou-Sleiman, PM and Healy, DG and Ariga, H and Wood, NW and de Silva, R and Revesz, T and Hardy, JA and Lees, AJ (2004) The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease. BRAIN , 127 420 - 430. 10.1093/brain/awh054.

Bandopadhyay, R and Kingsbury, AE and Evans, IM and Miller, DW and Cookson, MR and Lees, AJ (2004) DJ-1 immunoreactivity in control and idiopathic Parkinson's disease brain: Correlation with DJ-1 mRNA expression. In: MOVEMENT DISORDERS. (pp. S200 - S200). WILEY-LISS

Bandopadhyay, R. and Kingsbury, A.E. and Cookson, M.R. and Reid, A.R. and Evans, I.M. and Hope, A.D. and Pittman, A.M. and Lashley, T. and Canet-Aviles, R. and Miller, D.W. and McLendon, C. and Strand, C. and Leonard, A.J. and Abou-Sleiman, P.M. and Healy, D.G. and Ariga, H. and Wood, N.W. and de Silva, R. and Revesz, T. and Hardy, J.A. and Lees, A.J. (2004) The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease. Brain , 127 (2) pp. 420-430. 10.1093/brain/awh054.

Beck, J.A. and Poulter, M. and Campbell, T.A. and Uphill, J.B. and Adamson, G. and Geddes, J.F. and Revesz, T. and Davis, M.B. and Wood, N.W. and Collinge, J. and Tabrizi, S.J. (2004) Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease. Human Molecular Genetics , 13 (12) pp. 1219-1224. 10.1093/hmg/ddh134.

Beck, JA and Poulter, M and Campbell, T and Uphill, JB and Adamson, G and Geddes, JF and Revesz, T and Davis, M and Wood, NW and Collinge, J and Tabrizi, SJ (2004) Nuclear somatic mosaicism in sporadic early-onset Alzheimer's disease. In: NEUROBIOLOGY OF AGING. (pp. S54 - S54). ELSEVIER SCIENCE INC

Beck, JA and Poulter, M and Campbell, TA and Uphill, JB and Adamson, G and Geddes, JF and Revesz, T and Davis, MB and Wood, NW and Collinge, J and Tabrizi, SJ (2004) Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease. HUM MOL GENET , 13 (12) 1219 - 1224. 10.1093/hmg/ddh134.

Braendgaard, H and Josephs, K and Holton, J and Rossor, M and Gedde, A and Rosa, P and Waldemar, G and Revesz, T (2004) Neurofilament inclusion body disease (NIBD) - A new form of dementia. In: DEMENTIA AND GERIATRIC COGNITIVE DISORDERS. (pp. 370 - 370). KARGER

Bremner, FD and Houlden, H and Smith, SE (2004) Genotypic and phenotypic heterogeneity in familial microcoria. BRIT J OPHTHALMOL , 88 (4) 469 - 473. 10.1136/bjo.2003.027169.

Brown, AM and Gordon, D and Lee, H and Caudy, M and Hardy, J and Haroutunian, V and Blass, JP (2004) Association of the dihydrolipoamide dehydrogenase gene with Alzheimer's disease in an Ashkenazi Jewish population. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 131B (1) 60 - 66. 10.1002/ajmg.b.30008.

Brown, M. and Jacobs, T. and Eickholt, B. and Ferrari, G. and Teo, M. and Monfries, C. and Qi, R.Z. and Leung, T. and Lim, L. and Hall, C. (2004) {alpha}2-Chimaerin, cyclin-dependent kinase 5/p35, and its target collapsin response mediator protein-2 are essential components in semaphorin 3A-induced growth-cone collapse. Journal of Neuroscience , 24 (41) pp. 8994-9004. 10.1523/JNEUROSCI.3184-04.2004.
An open access version is available from UCL Discovery

Busby, J and O'Brien, KK and Gibson, AM and McKeith, IG and Perry, RH and Hardy, JA and Singleton, AB and Morris, CM (2004) Dementia with Lewy bodies: no association of polymorphisms in the human synphilin gene. NEUROGENETICS , 5 (4) 251 - 252. 10.1007/s10048-004-0188-x.

Busby, V and Goossens, S and Nowotny, P and Hamilton, G and Smemo, S and Harold, D and Turic, D and Jehu, L and Myers, A and Womick, M and Woo, D and Compton, D and Doil, LM and Tacey, KM and Lau, KF and Al-Saraj, S and Killick, R and Pickering-Brown, S and Moore, P and Hollingworth, P and Archer, N and Foy, C and Walter, S and Lendon, C and Iwatsubo, T and Morris, JC and Norton, J and Mann, D and Janssens, B and Hardy, J and O'Donovan, M and Jones, L and Williams, J and Holmans, P and Owen, MJ and Grupe, A and Powell, J and van Hengel, J and Goate, A and Van Roy, F and Lovestone, S (2004) alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease. NEUROMOLECULAR MEDICINE , 5 (2) 133 - 146. 10.1385/NMM:5:2:133.

C

Canevari, L and Abramov, AY and Duchen, MR (2004) Toxicity of amyloid beta peptide: Tales of calcium, mitochondria, and oxidative stress. NEUROCHEM RES , 29 (3) 637 - 650.

Cano, SJ and Hobart, JC and Fitzpatrick, R and Bhatia, K and Thompson, AJ and Warner, TT (2004) Patient-based outcomes of cervical dystonia: A review of rating scales. MOVEMENT DISORD , 19 (9) 1054 - 1059. 10.1002/mds.20055.

Cano, SJ and Warner, TT and Fitzpatrick, R and Bhatia, K and Thompson, AJ and Hobart, JC (2004) The cervical dystonia impact profile (CDIP-58): A new patient-based rating scale. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 1224 - 1224). B M J PUBLISHING GROUP

Cano, SJ and Warner, TT and Linacre, JM and Bhatia, KP and Thompson, AJ and Fitzpatrick, R and Hobart, JC (2004) Capturing the true burden of dystonia on patients - The Cervical Dystonia Impact Profile (CDIP-58). NEUROLOGY , 63 (9) 1629 - 1633.

Clark, LN and Afridi, S and Mejia-Santana, H and Harris, J and Louis, ED and Cote, LJ and Andrews, H and Singleton, A and De-Vrieze, FW and Hardy, J and Mayeux, R and Fahn, S and Waters, C and Ford, B and Frucht, S and Ottman, R and Marder, K (2004) Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations. MOVEMENT DISORDERS , 19 (7) 796 - 800. 10.1002/mds.20131.

Coleman, P and Kurlan, R and Crook, R and Werner, J and Hardy, J (2004) New presenilin Alzheimer's disease case confirms the helical alignment of pathogenic mutations in transmembrane domain 5. NEUROSCIENCE LETTERS , 364 (3) 139 - 140. 10.1016/j.neulet.2004.04.030.

Crowther, DC and Belorgey, D and Miranda, E and Kinghorn, KJ and Sharp, LK and Lomas, DA (2004) Practical genetics: alpha-1-antitrypsin deficiency and the serpinopathies. Eur J Hum Genet , 12 (3) 167 - 172. 10.1038/sj.ejhg.5201127.

Crowther, DC and Kinghorn, KJ and Page, R and Lomas, DA (2004) Therapeutic targets from a Drosophila model of Alzheimer's disease. Curr Opin Pharmacol , 4 (5) 513 - 516. 10.1016/j.coph.2004.07.001.

D

Davies, N and Beeson, D and Brownlow, S and Hanna, M (2004) Congenital myasthenic syndrome with episodic apnoea: new mutations and an unusual complication. In: JOURNAL OF NEUROLOGY. (pp. 16 - 16). DR DIETRICH STEINKOPFF VERLAG

de Silva, R and Lashley, T and Revesz, T and Lees, A and Powers, JM (2004) Detecting tau isoforms in archival cases. ACTA NEUROPATHOL , 107 (2) 181 - 182. 10.1007/s00401-003-0795-x.

de Silva, R and Pittman, AM and Myers, AJ and Wood, NW and Hardy, J and Lees, AJ (2004) Definition of the tau gene haplotype block that is associated with progressive supranuclear palsy. In: MOVEMENT DISORDERS. (pp. S355 - S355). WILEY-LISS

Depondt, C and Cavalleri, G and Weale, ME and Burly, MW and Cock, H and Shorvon, SD and Sisodiya, S and Wood, NW and Goldstein, DB (2004) Common variation in the SCN1A gene is a risk factor for common forms of epilepsy associated with febrile seizures. In: EPILEPSIA. (pp. 120 - 120). BLACKWELL PUBLISHING INC

Depondt, C and Cock, HR and Healy, DG and Burley, MW and Weinshenker, D and Wood, NW and Goldstein, DB and Sisodiya, SM (2004) The -1021C -> T DBH gene variant is not associated with epilepsy or antiepileptic drug response. NEUROLOGY , 63 (8) 1497 - 1499.

Dogu, O and Johnson, J and Hernandez, D and Hanson, M and Hardy, J and Apaydin, H and Ozekmekci, S and Sevim, S and Gwinn-Hardy, K and Singleton, A (2004) A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion. MOVEMENT DISORDERS , 19 (7) 812 - 816. 10.1002/mds.20028.

E

Emre, M. and Aarsland, D. and Albanese, A. and Byrne, E.J. and Deuschl, G. and De Deyn, P.P. and Durif, F. and Kulisevsky, J. and van Laar, T. and Lees, A. and Poewe, W. and Robillard, A. and Rosa, M.M. and Wolters, E. and Quarg, P. and Tekin, S. and Lane, R. (2004) Rivastigmine for dementia associated with Parkinson's disease. New England Journal of Medicine , 351 (24) pp. 2509-2518. 10.1056/NEJMoa041470.
An open access version is available from UCL Discovery

Evans, W and Fung, HC and Steele, J and Eerola, J and Tienari, P and Pittman, A and de Silva, R and Myers, A and Wavrant-De Vrieze, F and Singleton, A and Hardy, J (2004) The tau H2 haplotype is almost exclusively Caucasian in origin. NEUROSCI LETT , 369 (3) 183 - 185. 10.1016/j.neulet.2004.05.119.

Everett, CM and Wood, NW (2004) Trinucleotide repeats and neurodegenerative disease. BRAIN , 127 2385 - 2405. 10.1093/brain/awh278.

Evidente, VGH and Esteban, RP and Hernandez, JL and Natividad, FF and Advincula, J and Gwinn-Hardy, K and Hardy, J and Singleton, A and Singleton, A (2004) Smell testing is abnormal in 'lubag' or X-linked dystonia-parkinsonism: a pilot study. PARKINSONISM & RELATED DISORDERS , 10 (7) 407 - 410. 10.1016/j.parkreldis.2004.04.011.

F

Fidani, L and Goulas, A and Crook, R and Petersen, RC and Tangalos, E and Kotsis, A and Hardy, J (2004) An association study of the cholesteryl ester transfer protein TaqI B polymorphism with late onset Alzheimer's disease. NEUROSCIENCE LETTERS , 357 (2) 152 - 154. 10.1016/j.neulet.2003.11.071.

Furtado, S and Payami, H and Lockhart, PJ and Hanson, M and Nutt, JG and Singleton, AA and Singleton, A and Bower, J and Utti, RJ and Bird, TD and de la Fuente-Femandez, R and Tsuboi, Y and Klimek, ML and Suchowersky, O and Hardy, J and Calne, DB and Wszolek, ZK and Farrer, M and Gwinn-Hardy, K and Stoessl, AJ (2004) Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2). MOVEMENT DISORDERS , 19 (6) 622 - 629. 10.1002/mds.20074.

G

Gibb, GM and de Silva, R and Revesz, T and Lees, AJ and Anderton, BH and Hanger, DP (2004) Differential involvement and heterogeneous phosphorylation of tau isoforms in progressive supranuclear palsy. MOL BRAIN RES , 121 (1-2) 95 - 101. 10.1016/j.molbrainres.2003.11.007.

H

Hanna, MG (2004) Episodic ataxia and migraine. EUR J NEUROL , 11 341 - 341.

Hanson, M and Honour, M and Singleton, A and Crawley, A and Singleton, A and Hardy, J and Gwinn-Hardy, K (2004) Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity features. JOURNAL OF NEUROLOGY , 251 (11) 1398 - 1401. 10.1007/s00415-004-0552-7.

Hardy, J (2004) Is amyloid plaque imaging the key to monitoring brain pathology of Alzheimer's disease in vivo? For. EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING , 31 (11) 1539 - 1540. 10.1007/s00259-004-1676-9.

Hardy, J (2004) The uncertain anatomy of Alzheimer's disease. NEUROBIOLOGY OF AGING , 25 (6) 719 - 720. 10.1016/j.neurobiolaging.2003.12.012.

Hardy, J (2004) Toward Alzheimer therapies based on genetic knowledge. ANNUAL REVIEW OF MEDICINE , 55 15 - 25. 10.1146/annurev.med.55.091902.103607.

Hardy, J and Langston, JW (2004) How many pathways are there to nigral death? ANNALS OF NEUROLOGY , 56 (3) 316 - 318. 10.1002/ana.20257.

Hardy, J and Myers, A and Wavrant-De Vrieze, F (2004) Problems and Solutions in the Genetic Analysis of Late-Onset Alzheimer's Disease. NEURODEGENERATIVE DISEASES , 1 (4-5) 213 - 217. 10.1159/000080988.

Healy, DG and Abou-Sleiman, PM and Ahmadi, KR and Muqit, MMK and Bhatia, KP and Quinn, NP and Lees, AJ and Latchmann, DS and Goldstein, DB and Wood, NW (2004) The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonism. ANN NEUROL , 56 (3) 329 - 335.

Healy, DG and Abou-Sleiman, PM and Gibson, JM and Ross, OA and Jain, S and Gandhi, S and Gosal, D and Muqit, MMK and Wood, NW and Lynch, T (2004) PINK1 (PARK6) associated Parkinson disease in Ireland. NEUROLOGY , 63 (8) 1486 - 1488.

Healy, DG and Abou-Sleiman, PM and Lees, AJ and Casas, JP and Quinn, N and Bhatia, K and Hingorani, AD and Wood, NW (2004) Tau gene and Parkinson's disease: a case-control study and meta-analysis. J NEUROL NEUROSUR PS , 75 (7) 962 - 965. 10.1136/jnnp.2003.026203.

Healy, DG and Abou-Sleiman, PM and Ozawa, T and Lees, AJ and Bhatia, K and Ahmadi, KR and Wullner, U and Berciano, J and Moller, JC and Kamm, C and Burk, K and Barrone, P and Tolosa, E and Quinn, N and Goldstein, DB and Wood, NW (2004) A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's disease. ANN NEUROL , 55 (3) 443 - 446.

Healy, DG and Abou-Sleiman, PM and Valente, EM and Gilks, WP and Bhatia, K and Quinn, N and Lees, AJ and Wood, NW (2004) DJ-1 mutations in Parkinson's disease. J NEUROL NEUROSUR PS , 75 (1) 144 - 145.

Healy, DG and Abou-Sleiman, PM and Wood, NW (2004) Genetic causes of Parkinson's disease: UCHL-1. CELL TISSUE RES , 318 (1) 189 - 194. 10.1007/s00441-004-0917-3.

Healy, DG and Abou-Sleiman, PM and Wood, NW (2004) PINK, PANK, or PARK? A clinicians' guide to familial parkinsonism. LANCET NEUROL , 3 (11) 652 - 662.

Healy, DG and Wood, NW (2004) Clinical picture of bilateral vestibular schwannomas, sudden bilateral hearing loss, and aviation. NEUROLOGY , 63 (5) 933 - 933.

Henley, SM and Warrington, EK and Warner, TT and Stevens, JM and Ashburner, J and Rossor, MN and Fox, NC and Tabrizi, SJ (2004) Correlation between patterns of atrophy and psychomotor task performance in early Huntington's disease. In: NEUROBIOLOGY OF AGING. (pp. S462 - S462). ELSEVIER SCIENCE INC

Hodgetts, A and Bosse, JT and Kroll, JS and Langford, PR (2004) Analysis of differential protein expression in Actinobacillus pleuropneumoniae by Surface Enhanced Laser Desorption Ionisation-ProteinChip (TM) (SELDI) technology. VET MICROBIOL , 99 (3-4) 215 - 225. 10.1016/j.vetmic.2004.01.003.

Hope, AD and Lashley, T and Lees, AJ and de Silva, R (2004) Failure in heat-shock protein expression in response to UBB+1 protein in progressive supranuclear palsy in humans. NEUROSCI LETT , 359 (1-2) 94 - 98. 10.1016/j.neulet.2003.12.0127.

Hope, AD and Lashley, T and Lees, AJ and de Silva, R (2004) Failure in heat-shock protein expression in response to UBB+1 protein in progressive supranuclear palsy in humans. Neurosci Lett , 359 (1-2) 94 - 98. 10.1016/j.neulet.2003.12.127.

Houlden, H and Blake, J and Reilly, MM (2004) Hereditary sensory neuropathies. CURR OPIN NEUROL , 17 (5) 569 - 577.

Houlden, H and Girard, M and Cockerell, C and Ingram, D and Wood, NW and Goossens, M and Walker, RWH and Reilly, MM (2004) Connexin 32 promoter P2 mutations: A mechanism of peripheral nerve dysfunction. ANN NEUROL , 56 (5) 730 - 734. 10.1002/ana.20267.

Houlden, H and King, RHM and Muddle, JR and Warner, TT and Reilly, MM and Orrell, RW and Ginsberg, L (2004) A novel RAB7 mutation associated with ulcero-mutilating neuropathy. ANN NEUROL , 56 (4) 586 - 590. 10.1002/ana.20281.

Houlden, H and King, RHM and Muddle, JR and Warner, TT and Reilly, MM and Orrell, RW and Ginsberg, L (2004) Ulcero-mutilating neuropathy: Clinical, pathological and molecular genetic study of a family with a novel RAB7 mutation. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 1228 - 1228). B M J PUBLISHING GROUP

Houlden, H. and Girard, M. and Cockerell, C. and Ingram, D. and Wood, N.W. and Goossens, M. and Walker, R.W.H. and Reilly, M.M. (2004) Connexin 32 promoter P2 mutations: a mechanism of peripheral nerve dysfunction. Annals of Neurology , 56 (5) pp. 730-734. 10.1002/ana.20267.

Houlden, H. and King, R.H.M. and Muddle, J.R. and Warner, T.T. and Reilly, M.M. and Orrell, R.W. and Ginsberg, L. (2004) A novel RAB7 mutation associated with ulcero-mutilating neuropathy. Annals of Neurology , 56 (4) pp. 586-590. 10.1002/ana.20281.

I

Imbrici, P and Jaffe, SL and Eunson, LH and Davies, NP and Herd, C and Robertson, R and Kullmann, DM and Hanna, MG (2004) Dysfunction of the brain calcium channel Ca(V)2.1 in absence epilepsy and episodic ataxia. BRAIN , 127 2682 - 2692. 10.1093/brain/awh301.

Imbrici, P. and Jaffe, S.L. and Eunson, L.H. and Davies, N.P. and Herd, C. and Robertson, R. and Kullmann, D.M. and Hanna, M.G. (2004) Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia. Brain , 127 (12) pp. 2682-2692. 10.1093/brain/awh301.

Isenberg, DA and Allen, E and Farewell, V and Ehrenstein, MR and Hanna, MG and Lundberg, IE and Oddis, C and Pilkington, C and Plotz, P and Scott, D and Vencovsky, J and Cooper, R and Rider, L and Miller, F and Int Myositis Clinical Studies Grp, (2004) International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in patients with adult onset disease. RHEUMATOLOGY , 43 (1) 49 - 54. 10.1093/rheumatology/keg427.

J

Johnson, J and Hague, SM and Hanson, M and Gibson, A and Wilson, KE and Evans, EW and Singleton, AA and McInerney-Leo, A and Nussbaum, RL and Hernandez, DG and Gallardo, M and McKeith, IG and Burn, DJ and Ryu, M and Hellstrom, O and Ravina, B and Eerola, J and Perry, RH and Jaros, E and Tienari, P and Weiser, R and Gwinn-Hardy, K and Morris, CM and Hardy, J and Singleton, AB (2004) SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies. NEUROLOGY , 63 (3) 554 - 556.

Johnson, J and Ostojic, J and Lannfelt, L and Glaser, A and Basun, H and Rogaeva, E and Kawarai, T and Bruni, A and Hyslop, PHSG and Goate, A and Pastor, P and Chakraverty, S and Norton, J and Morris, JC and Hardy, J and Singleton, A (2004) No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found. NEUROSCIENCE LETTERS , 363 (2) 99 - 101. 10.1016/j.neulet.2004.03.070.

Josephs, KA and Holton, JL and Rossor, MN and Godbolt, AK and Ozawa, T and Strand, K and Khan, N and Al-Sarraj, S and Revesz, T (2004) Frontotemporal lobar degeneration and ubiquitin immunohistochemistry. NEUROPATH APPL NEURO , 30 (4) 369 - 373. 10.1111/j.1365-2990.2004.00545.x.

Josephs, KA and Holton, JL and Rossor, MN and Godbolt, AK and Ozawa, T and Strand, K and Khan, N and Al-Sarraj, S and Revesz, T (2004) Frontotemporal lobar degeneration and ubiquitin immunohistochemistry. Neuropathol Appl Neurobiol , 30 (4) 369 - 373. 10.1111/j.1365-2990.2003.00545.x.

K

Khan, NL and Katzenschlager, R and Watt, H and Bhatia, KP and Wood, NW and Quinn, N and Lees, AJ (2004) Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease. NEUROLOGY , 62 (7) 1224 - 1226.

Kinali, M and Jungbluth, H and Eunson, LH and Sewry, CA and Manzur, AY and Mercuri, E and Hanna, MG and Muntoni, F (2004) Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia. NEUROMUSCULAR DISORD , 14 (10) 689 - 693. 10.1016/j.nmd.2004.06.007.

Kuo, L and An, SF and Groves, MJ and Lee, C and Scaravilli, F (2004) Gene expression profile in rat dorsal root ganglion (DRG) following sciatic nerve transection and systemic neurotrophin-3 (NT-3) administration. In: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. (pp. 516 - 516). AMER ASSN NEUROPATHOLOGISTS INC

L

Lashley, T and Holton, JL and Frangione, B and Bandopadhyay, R and Ghiso, J and Rostagno, A and Revesz, T (2004) The possible origin of the amyloid peptides in the BRI2 gene-related dementias. In: NEUROBIOLOGY OF AGING. (pp. S171 - S171). ELSEVIER SCIENCE INC

Lee, C and Scaravilli, F and Kuo, L and Wang, C and An, SF (2004) Accumulation of prion protein in the peripheral nervous system of human forms of the disease: An immunohistochemical study. In: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. (pp. 515 - 515). AMER ASSN NEUROPATHOLOGISTS INC

Lee, MJ and Stephenson, D and Groves, M and Sweeney, M and Davis, M and An, SF and Houlden, H and Scaravilli, F and Wood, N and Reilly, M (2004) Sensory deprivation is associated with a mutation in the rat chaperonin delta subunit. In: GENETICAL RESEARCH. (pp. 120 - 120). CAMBRIDGE UNIV PRESS

Li, C and Varsani, H and Maillard, S and Jones, R and Holton, J and Woo, P and Wedderburn, LR (2004) Do histological features parallel clinical severity in Juvenile Dermatomyositis: Proposal of a novel scoring system. In: Clin.Exp.Rheumatol. (pp. 529 - 529).

Li, CKC and Varsani, H and Holton, JL and Gao, B and Woo, P and Wedderburn, LR and Juvenile Dermatomyositis Res Grp, (2004) MHC class I overexpression on muscles in early juvenile derma-tomyositis. J RHEUMATOL , 31 (3) 605 - 609.

Li, Y and Nowotny, P and Holmans, P and Smemo, S and Kauwe, JSK and Hinrichs, AL and Tacey, K and Doil, L and van Luchene, R and Garcia, V and Rowland, C and Schrodi, S and Leong, D and Gogic, G and Chan, J and Cravchik, A and Ross, D and Lau, K and Kwok, S and Chang, SY and Catanese, J and Sninsky, J and White, TJ and Hardy, J and Powell, J and Lovestone, S and Morris, JC and Thal, L and Owen, M and Williams, J and Goate, A and Grupe, A (2004) Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , 101 (44) 15688 - 15693. 10.1073/pnas.0403535101.

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