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Number of items: 193.

A

Abramov, A.Y.; Jacobson, J.; Wientjes, F.; Hothersall, J.; Canevari, L.; Duchen, M.R.; (2005) Expression and modulation of an NADPH oxidase in mammalian astrocytes. Journal of Neuroscience , 25 (40) pp. 9176-9184. 10.1523/JNEUROSCI.1632-05.2005. Green open access
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Abramov, AY; Canevari, L; Duchen, MR; (2005) Expression, function and modulation of an NADPH oxidase in mammalian astrocytes. In: BIOPHYSICAL JOURNAL. (pp. 256A - 257A). BIOPHYSICAL SOCIETY

Abramov, AY; Duchen, MR; (2005) Mechanisms underlying the loss of mitochondrial potential calcium homeostasis in neurons during glutamate excitotoxicity. In: JOURNAL OF NEUROCHEMISTRY. (pp. 246 - 246).

Abramov, AY; Duchen, MR; (2005) The role of an astrocytic NADPH oxidase in the neurotoxicity of amyloid beta peptides. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES , 360 (1464) 2309 - 2314. 10.1098/rstb.2005.1766. Gold open access

Abramov, AY; Jacobson, J; Wientjes, F; Hothersall, J; Canevari, L; Duchen, MR; (2005) Expression and modulation of an NADPH oxidase in mammalian astrocytes. J NEUROSCI , 25 (40) 9176 - 9184. 10.1523/JNEUROSCI.1632-05.2005.

Ahmadi, K.R.; Weale, M.E.; Xue, Z.Y.; Soranzo, N.; Yarnall, D.P.; Briley, J.D.; ... Goldstein, D.B.; + view all (2005) A single-nucleotide polymorphism tagging set for human drug metabolism and transport. Nature Genetics , 37 (1) pp. 84-89. 10.1038/ng1488.

Ahmadi, KR; Weale, ME; Xue, ZYY; Soranzo, N; Yarnall, DP; Briley, JD; ... Goldstein, DB; + view all (2005) A single-nucleotide polymorphism tagging set for human drug metabolism and transport. NAT GENET , 37 (1) 84 - 89. 10.1038/ng1488.

Almqvist, J; Zou, J; Liderson, Y; Pettersson, S; Ernberg, I; Borestrom, C; ... Altiok, E; + view all (2005) Functional interaction of Oct transcription factors with the family of repeats in Epstein-Barr virus oriP. Journal of General Virology , 86 (5) 1261 - 1267. 10.1099/vir.0.80620-0.

Almqvist, J; Zou, J; Linderson, Y; Borestrom, C; Altiok, E; Zetterberg, H; ... Ernberg, I; + view all (2005) Functional interaction of Oct transcription factors with the family of repeats in Epstein-Barr virus oriP. J Gen Virol , 86 (Pt 5) 1261 - 1267. 10.1099/vir.0.80620-0.

Archer, HA; Schott, JM; Barnes, J; Fox, NC; Holton, JL; Revesz, T; ... Rossor, MN; + view all (2005) Knight's move thinking? Mild cognitive impairment in a chess player. NEUROCASE , 11 (1) 26 - 31. 10.1080/13554790490896875.

B

Bandopadhyay, R; Kingsbury, AE; Lees, AJ; (2005) Expression pattern of synphilin-1 and parkin in control and Parkinson's disease brain. In: MOVEMENT DISORDERS. (pp. S122 - S122). WILEY-LISS

Bandopadhyay, R; Kingsbury, AE; Muqit, MM; Harvey, K; Reid, AR; Kilford, L; ... Lees, AJ; + view all (2005) Synphilin-1 and parkin show overlapping expression patterns in human brain and form aggresomes in response to proteasomal inhibition. NEUROBIOL DIS , 20 (2) 401 - 411. 10.1016/j.nbd.2005.03.021.

Bandopadhyay, R; Miller, DW; Kingsbury, AE; Jowett, TP; Kaleem, MM; Pittman, AM; ... Lees, AJ; + view all (2005) Development, characterisation and epitope mapping of novel monoclonal antibodies for DJ-1 (PARK7) protein. NEUROSCI LETT , 383 (3) 225 - 230. 10.1016/j.neulet.2005.04.024.

Bengtson, P; Zetterberg, H; Mellberg, T; Påhlsson, P; Larson, G; (2005) Characterization of EBV-transformed B-cells established from an individual homozygously mutated (G329A) in the FUT7 alpha1,3-fucosyltransferase gene. Scand J Immunol , 62 (3) 251 - 258. 10.1111/j.1365-3083.2005.01650.x.

Blennow, K; Johansson, A; Zetterberg, H; (2005) Diagnostic value of 14-3-3beta immunoblot and T-tau/P-tau ratio in clinically suspected Creutzfeldt-Jakob disease. Int J Mol Med , 16 (6) 1147 - 1149.

Blennow, K; Popa, C; Rasulzada, A; Minthon, L; Wallin, A; Zetterberg, H; (2005) [There is a strong evidence that professional boxing results in chronic brain damage. The more head punches during a boxer's career, the bigger is the risk]. Lakartidningen , 102 (36) 2468 - 2475.

Blennow, K; Wallin, A; Popa, C; Rasulzada, A; Minthon, L; Zetterberg, H; (2005) Starka belägg för att proffsboxning leder till kroniska hjärnskador. Lakartidningen , 102 (36) 2468 - 2475.

Bobb, AJ; Addington, AM; Sidransky, E; Gornick, MC; Lerch, JP; Greenstein, DK; ... Rapoport, JL; + view all (2005) Support for association between ADHD and two candidate genes: NET1 and DRD1. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 134B (1) 67 - 72. 10.1002/ajmg.b.30142.

Borhani-Haghighi, A; Houlden, H; Lankarani, KB; Taghavi, A; Masnadi, K; (2005) A novel sequence variation in the first genetically confirmed Allgrove syndrome in Iran. In: JOURNAL OF NEUROLOGY. (pp. 59 - 59). DR DIETRICH STEINKOPFF VERLAG

Bras, JM; Guerreiro, RJ; Ribeiro, MH; Januario, C; Morgadinho, A; Oliveira, CR; ... Singleton, A; + view all (2005) G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort. MOVEMENT DISORD , 20 (12) 1653 - 1655.

C

Cavalleri, GL; Lynch, JM; Depondt, C; Burley, MW; Wood, NW; Sisodiya, SM; Goldstein, DB; (2005) Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here? BRAIN , 128 1832 - 1840. 10.1093/brain/awh524.

Cavallieri, GL; Kinirons, P; Shahwan, A; McCarthy, M; Doherty, CP; Wood, NW; ... Delanty, N; + view all (2005) Genetic variation in GABAG2 - Lessons to be learned from association studies in two large epilepsy cohorts. In: EPILEPSIA. (pp. 366 - 366). BLACKWELL PUBLISHING

Clarimon, J; Asgeirsson, H; Singleton, A; Jakobsson, F; Hjaltason, H; Hardy, J; Sveinbjornsdottir, S; (2005) Torsin A haplotype predisposes to idiopathic dystonia. ANNALS OF NEUROLOGY , 57 (5) 765 - 767. 10.1002/ana.20485.

Clarimon, J; Johnson, J; Dogu, O; Horta, W; Khan, N; Lees, AJ; ... Singleton, A; + view all (2005) Defining the ends of Parkin Exon 4 deletions in two different families with Parkinson's disease. AM J MED GENET B , 133B (1) 120 - 123. 10.1002/ajmg.b.30119.

Coolen, MW; Van Loo, KM; Van Bakel, NN; Pulford, DJ; Serneels, L; De Strooper, B; ... Martens, GJ; + view all (2005) Gene dosage effect on gamma-secretase component Aph-1b in a rat model for neurodevelopmental disorders. Neuron , 45 (4) 497 - 503. 10.1016/j.neuron.2004.12.054.

Crowther, DC; Kinghorn, KJ; Miranda, E; Page, R; Curry, JA; Duthie, FA; ... Lomas, DA; + view all (2005) Intraneuronal Abeta, non-amyloid aggregates and neurodegeneration in a Drosophila model of Alzheimer's disease. Neuroscience , 132 (1) 123 - 135. 10.1016/j.neuroscience.2004.12.025.

D

Davies, N.P.; Imbrici, P.; Fialho, D.; Herd, C.; Bilsland, L.G.; Weber, A.; ... Hanna, M.G.; + view all (2005) Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation. Neurology , 65 (7) pp. 1083-1089. 10.1212/01.wnl.0000178888.03767.74.

Davies, NP; Imbrici, P; Fialho, D; Herd, C; Bilsland, LG; Giunti, P; ... Lehmann-Horn, F; + view all (2005) Andersen-Tawil syndrome: New potassium channel mutations and possible phenotypic variation. Neurology , 65 (7) 1083 - 1089. 10.1212/01.wnl.0000178888.03767.74.

Davies, NP; Imbrici, P; Fialho, D; Herd, C; Bilsland, LG; Weber, A; ... Hanna, MG; + view all (2005) Andersen-Tawil syndrome - New potassium channel mutations and possible phenotypic variation. NEUROLOGY , 65 (7) 1083 - 1089.

De Strooper, B; (2005) Nicastrin: gatekeeper of the gamma-secretase complex. Cell , 122 (3) 318 - 320. 10.1016/j.cell.2005.07.021.

Depondt, C; Cavalleri, GL; Shorvon, SD; Wood, NW; Sisodiya, SM; Goldstein, DB; (2005) Association study of five sodium channel genes in epilepsy and antiepileptic drug response. In: EPILEPSIA. (pp. 90 - 91). BLACKWELL PUBLISHING

Dominguez, D; Tournoy, J; Hartmann, D; Huth, T; Cryns, K; Deforce, S; ... De Strooper, B; + view all (2005) Phenotypic and biochemical analyses of BACE1- and BACE2-deficient mice. J Biol Chem , 280 (35) 30797 - 30806. 10.1074/jbc.M505249200.

E

Edwards-Lee, T; Ringman, JM; Chung, J; Werner, J; Morgan, A; Hyslop, PS; ... Hardy, J; + view all (2005) An African American family with earlyonset Alzheimer disease and an APP (T714I) mutation. NEUROLOGY , 64 (2) 377 - 379.

Eriksson, S; Trupke, M; Powell, HF; Sahagun, D; Sinclair, CDJ; Curtis, EA; ... Kraft, M; + view all (2005) Integrated optical components on atom chips. EUR PHYS J D , 35 (1) 135 - 139. 10.1140/epjd/e2005-00092-x.

Eunson, LH; Graves, TD; Hanna, MG; (2005) New calcium channel mutations predict aberrant RNA splicing in episodic ataxia. NEUROLOGY , 65 (2) 308 - 310.

Eunson, LH; Graves, TD; Hanna, MG; (2005) New calcium channel mutations predict aberrant RNA splicing in episodic ataxia. Neurology , 65 (2) 308 - 310. 10.1212/01.wnl.0000169020.82223.dd.

Everett, CM; Graves, TD; Lad, S; Jager, HR; Thom, M; Isenberg, DA; Hanna, MG; (2005) CNS Lupus in the absence of systemic disease activity. In: JOURNAL OF THE NEUROLOGICAL SCIENCES. (pp. S271 - S271). ELSEVIER SCIENCE BV

F

Fung, HC; Evans, J; Evans, W; Duckworth, J; Pittman, A; de Silva, R; ... Hardy, J; + view all (2005) The architecture of the tau haplotype block in different ethnicities. NEUROSCI LETT , 377 (2) 81 - 84. 10.1016/j.neulet.2004.11.072.

G

Gandhi, S; Abou-Sleiman, PM; Healy, DG; Weale, M; Gilks, W; Ahmadi, K; ... Wood, NW; + view all (2005) Population genetic approaches to neurological disease: Parkinson's disease as an example. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES , 360 (1460) 1573 - 1578. 10.1098/rstb.2005.1687. Gold open access

Gandhi, S; Muqit, M; Ganguly, M; Abou-Sleiman, PM; Wood, NW; Holton, JL; Revesz, T; (2005) PINK1 protein distribution in normal human brain and Parkinson's disease. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 221 - 222). BLACKWELL PUBLISHING LTD

Gandhi, S; Wood, NW; (2005) Molecular pathogenesis of Parkinson's disease. Hum Mol Genet , 14 (18) 2749 - 2755. 10.1093/hmg/ddi308.

Gandhi, S; Wood, NW; (2005) Molecular pathogenesis of Parkinson's disease. Hum Mol Genet , 14 Spec No. 2 2749 - 2755.

Geser, F; Seppi, K; Stampfer-Kountchev, M; Kollensperger, M; Diem, A; Ndayisaba, JP; ... EMSA-SG,; + view all (2005) The European Multiple System Atrophy-Study Group (EMSA-SG). JOURNAL OF NEURAL TRANSMISSION , 112 (12) 1677 - 1686. 10.1007/s00702-005-0328-y.

Gilks, W.P.; Abou-Sleiman, P.M.; Gandhi, S.; Jain, S.; Singleton, A.; Lees, A.J.; ... Wood, N.W.; + view all (2005) A common LRRK2 mutation in idiopathic Parkinson's disease. The Lancet , 365 (9457) pp. 415-416. 10.1016/S0140-6736(05)17830-1.

Gilks, WP; Abou-Sleiman, PM; Gandhi, S; Jain, S; Singleton, A; Lees, AJ; ... Wood, NW; + view all (2005) Common LRRK2 mutation in idiopathic Parkinson's disease. LANCET , 365 (9457) 415 - 416.

Gioltzoglou, T; Cordivari, C; Lee, PJ; Hanna, MG; Lees, AJ; (2005) Problems with botulinum toxin treatment in mitochondrial cytopathy: case report and review of the literature. J NEUROL NEUROSUR PS , 76 (11) 1594 - 1596. 10.1136/jnnp.2004.057661.

Godbolt, AK; Josephs, KA; Revesz, T; Warrington, EK; Lantos, P; King, A; ... Rossor, MN; + view all (2005) Sporadic and familial dementia with ubiquitin-positive tau-negative inclusions - Clinical features of one histopathological abnormality underlying frontotemporal lobar degeneration. ARCH NEUROL-CHICAGO , 62 (7) 1097 - 1101.

Graves, T; Imbrici, P; Eunson, L; Bhatia, KP; Wodia, NH; Hanna, MG; Kullmann, DM; (2005) Late onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 156 - 157). B M J PUBLISHING GROUP

Graves, TD; Hanna, MG; (2005) Neurological channelopathies. POSTGRAD MED J , 81 (951) 20 - 32. 10.1136/pgmj.2004.022012. Gold open access

Grimm, MO; Grimm, HS; Pätzold, AJ; Zinser, EG; Halonen, R; Duering, M; ... Hartmann, T; + view all (2005) Regulation of cholesterol and sphingomyelin metabolism by amyloid-beta and presenilin. Nat Cell Biol , 7 (11) 1118 - 1123. 10.1038/ncb1313.

H

Hanna, MG; Cudia, P; (2005) Peripheral Nerve Diseases Associated with Mitochondrial Respiratory Chain Dysfunction. In: UNSPECIFIED (1937 - 1949).

Hanna, MG; Graves, TD; Jaffe, S; Imbrici, P; Kullmann, DM; (2005) Dysfunction of the brain calcium channel Ca(V)2.1 in absence epilepsy and episodic ataxia - authors' response. BRAIN , 128 ? - ?. 10.1093/brain/awh439.

Hardy, J; (2005) Expression of normal sequence pathogenic proteins for neurodegenerative disease contributes to disease risk: 'permissive templating' as a general mechanism underlying neurodegeneration. In: BIOCHEMICAL SOCIETY TRANSACTIONS. (pp. 578 - 581).

Hardy, J; Lees, AJ; (2005) Parkinson's disease: A broken nosology. MOVEMENT DISORDERS , 20 S2 - S4. 10.1002/mds.20532.

Hardy, J; Pittman, A; Myers, A; Gwinn-Hardy, K; Fung, HC; de Silva, R; ... Duckworth, J; + view all (2005) Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens. BIOCHEMICAL SOCIETY TRANSACTIONS , 33 582 - 585.

Healy, DG; Abou-Sleiman, PM; Quinn, N; Ahmadi, KR; Ozawa, T; Kamm, C; ... European MSA Study Grp,; + view all (2005) UCHL-1 gene in multiple system atrophy: A haplotype tagging approach. MOVEMENT DISORD , 20 (10) 1338 - 1343. 10.1002/mds.20575.

Henley, SM; Warner, TT; Warrington, EK; Stevens, JM; Ashburner, J; Fox, NC; (2005) Longitudinal changes in MRI and neuropsychological measures in early Huntington's disease - A pilot study. In: MOVEMENT DISORDERS. (pp. S9 - S9). WILEY-LISS

Henley, SMD; Warrington, EK; Frost, C; MacManus, DG; Warner, TT; Fox, NC; Tabrizi, SJ; (2005) Mri and cognitive changes detectable over 6 and 12 months in early Huntington's disease. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. ? - ?). B M J PUBLISHING GROUP

Hernandez, D; Paisan Ruiz, C; Crawley, A; Malkani, R; Werner, J; Gwinn-Hardy, K; ... Singleton, A; + view all (2005) The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases. Neurosci Lett , 389 (3) 137 - 139. 10.1016/j.neulet.2005.07.044.

Hernandez, DG; Paisan-Ruiz, C; McInerney-Leo, A; Jain, S; Meyer-Lindenberg, A; Evans, EW; ... Singleton, AB; + view all (2005) Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. ANN NEUROL , 57 (3) 453 - 456. 10.1002/ana.20401.

Holmans, P; Hamshere, M; Hollingworth, P; Rice, F; Tunstall, N; Jones, S; ... Williams, J; + view all (2005) Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 135B (1) 24 - 32. 10.1002/ajmg.b.30114.

Holton, JL; Revesz, T; Bhardwaj, N; Venner, K; Vicart, P; Goldfarb, L; Clarke, C; (2005) A novel desmin mutation associated with skeletal myopathy and heart block. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 239 - 239). BLACKWELL PUBLISHING LTD

Horga, A; Hernández-Vara, J; López, A; Río, J; Navarrete, M; Purroy, F; Álvarez-Sabín, J; (2005) [Primary central nervous system lymphoma in immunocompetent patients: retrospective study of thirteen cases]. In: Neurologia. (pp. 499 - ?). Elsevier

Houlden, H; King, RHM; Blake, J; Jacobs, J; Groves, MJ; Love, S; ... Reilly, MM; + view all (2005) Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I). In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. 35 - 35). BLACKWELL PUBLISHING

Houlden, H; Roper, H; Blake, J; Reilly, MM; (2005) Manifesting carriers and genetic heterogeneity in giant axonal neuropathy. In: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. (pp. 35 - 35). BLACKWELL PUBLISHING

Huang, CS; Shi, SH; Ule, J; Ruggiu, M; Barker, LA; Darnell, RB; ... Jan, LY; + view all (2005) Common molecular pathways mediate long-term potentiation of synaptic excitation and slow synaptic inhibition. Cell , 123 (1) 105 - 118. 10.1016/j.cell.2005.07.033.

Huppert, SS; Ilagan, MX; De Strooper, B; Kopan, R; (2005) Analysis of Notch function in presomitic mesoderm suggests a gamma-secretase-independent role for presenilins in somite differentiation. Dev Cell , 8 (5) 677 - 688. 10.1016/j.devcel.2005.02.019.

I

Imbrici, P; Eunson, LH; Graves, TD; Bhatia, KP; Wadia, NH; Kullmann, DM; Hanna, MG; (2005) Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A. NEUROLOGY , 65 (6) 944 - 946.

Iwata, O.; Thornton, J.S.; Sellwood, M.W.; Iwata, S.; Sakata, Y.; Noone, M.A.; ... Robertson, N.J.; + view all (2005) Depth of delayed cooling alters neuroprotection pattern after hypoxia-ischemia. Annals of Neurology , 58 (1) pp. 75-87. 10.1002/ana.20528.

J

Jain, S; Wood, NW; Healy, DG; (2005) Molecular genetic pathways in Parkinson's disease: a review. CLIN SCI , 109 (4) 355 - 364. 10.1042/CS0050106.

Jain, S; Wood, NW; Healy, DG; (2005) Molecular genetic pathways in Parkinson's disease: a review. Clin Sci (Lond) , 109 (4) 355 - 364. 10.1042/CS20050106.

Johansson, A; Zetterberg, H; Hampel, H; Buerger, K; Prince, JA; Minthon, L; ... Blennow, K; + view all (2005) Genetic association of CDC2 with cerebrospinal fluid tau in Alzheimer's disease. Dement Geriatr Cogn Disord , 20 (6) 367 - 374. 10.1159/000088634.

Johansson, A; Zetterberg, H; Håkansson, A; Nissbrandt, H; Blennow, K; (2005) TAU haplotype and the Saitohin Q7R gene polymorphism do not influence CSF Tau in Alzheimer's disease and are not associated with frontotemporal dementia or Parkinson's disease. Neurodegener Dis , 2 (1) 28 - 35. 10.1159/000086428.

K

Kamm, C; Healy, DG; Quinn, NP; Wullner, U; Moller, JC; Schols, L; ... EMSA Study Grp,; + view all (2005) The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group. BRAIN , 128 1855 - 1860. 10.1093/brain/awh535.

Khan, NL; Giunti, P; Sweeney, MG; Scherfler, C; Brien, MO; Piccini, P; ... Lees, AJ; + view all (2005) Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6). MOVEMENT DISORD , 20 (9) 1115 - 1119. 10.1002/mds.20564.

Khan, NL; Horta, W; Eunson, L; Graham, E; Johnson, JO; Chang, S; ... Lees, AJ; + view all (2005) Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years. MOVEMENT DISORD , 20 (4) 479 - 484. 10.1002/mds.20335.

Khan, NL; Jain, S; Lynch, JM; Pavese, N; Abou-Sleiman, P; Holton, JL; ... Wood, NW; + view all (2005) Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data. BRAIN , 128 2786 - 2796. 10.1093/brain/awh667.

Khan, NL; Scherfler, C; Graham, E; Bhatia, KP; Quinn, N; Lees, AJ; ... Piccini, P; + view all (2005) Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation. NEUROLOGY , 64 (1) 134 - 136.

Kumar-Singh, S; Pirici, D; McGowan, E; Serneels, S; Ceuterick, C; Hardy, J; ... Van Broeckhoven, C; + view all (2005) Dense-core plaques in Tg2576 and PSAPP mouse models of Alzheimer's disease are centered on vessel walls. AMERICAN JOURNAL OF PATHOLOGY , 167 (2) 527 - 543. 10.1016/S0002-9440(10)62995-1.

Kuo, LT; Simpson, A; Schanzer, A; Tse, J; An, SF; Scaravilli, F; Groves, MJ; (2005) Effects of systemically administered NT-3 on sensory neuron loss and nestin expression following axotomy. J COMP NEUROL , 482 (4) 320 - 332. 10.1002/cne.20400.

L

Lahiri, DK; Ge, YW; Maloney, B; Wavrant-De Vrieze, F; Hardy, J; (2005) Characterization of two APP gene promoter polymorphisms that appear to influence risk of late-onset Alzheimer's disease. NEUROBIOLOGY OF AGING , 26 (10) 1329 - 1341. 10.1016/j.neurobiolaging.2004.11.005.

Lashley, T; Holton, JL; Frangione, B; van Horssen, J; Rostagno, A; Verbeek, MM; ... Revesz, T; + view all (2005) Amyloid-associated proteins (AAPs) in familial British dementia (FBD) and familial Danish dementia (FDD). In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 244 - 244). BLACKWELL PUBLISHING LTD

Lee, CCM; Kuo, LT; Wang, CH; Scaravilli, F; An, SF; (2005) Accumulation of prion protein in the peripheral nervous system in human prion diseases. J NEUROPATH EXP NEUR , 64 (8) 716 - 721.

Leyssen, M; Ayaz, D; Hébert, SS; Reeve, S; De Strooper, B; Hassan, BA; (2005) Amyloid precursor protein promotes post-developmental neurite arborization in the Drosophila brain. EMBO J , 24 (16) 2944 - 2955. 10.1038/sj.emboj.7600757.

Li, C; Holton, JL; Varsani, H; Weaver, N; Harding, B; Woo, P; Wedderburn, LR; (2005) Initial histological features in juvenile dermatomyositis may predict clinical progression. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 230 - 230). BLACKWELL PUBLISHING LTD

Li, CKC; Holton, JL; Varsani, H; Woo, P; Wedderburn, LR; (2005) Histological features in juvenile dermatomyositis may predict clinical progression. In: RHEUMATOLOGY. (pp. I92 - I93). OXFORD UNIV PRESS

Li, Y; Rowland, C; Tacey, K; Catanese, J; Sninsky, J; Hardy, J; ... Grupe, A; + view all (2005) The BDNF val66met polymorphism is not associated with late onset Alzheimer's disease in three case-control samples. MOLECULAR PSYCHIATRY , 10 (9) 809 - 810. 10.1038/sj.mp.4001702.

Li, YH; Hollingworth, P; Moore, P; Foy, C; Archer, N; Powell, J; ... Grupe, A; + view all (2005) Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. HUMAN MUTATION , 25 (3) 270 - 277. 10.1002/humu.20138.

Lima, M; Montiel, R; Silva, C; Bettencourt, C; Costa, MC; Maciel, P; ... Coutinho, P; + view all (2005) Population genetics of wild-type CAG repeats in the Machado-Joseph Disease gene in Portugal. Human Heredity , 60 (3) 156 - 163. 10.1159/000090035.

Liolitsa, D; McKenzie, M; Hargreaves, I; Heales, S; Land, J; Sisodiya, SM; ... Hanna, MG; + view all (2005) MELAS, a young-onset stroke disorder associated with a homoplasmic ND5 mitochondrial DNA mutation. EUR J NEUROL , 12 158 - 159.

Llorente-Garcia, I; Sinclair, CDJ; Curtis, EA; Eriksson, S; Sauer, BE; Hinds, EA; (2005) Permanent-magnet atom chips for the study of long, thin atom clouds. In: Weiner, J and Feenstra, L and Schmiedmayer, J, (eds.) (Proceedings) International Conference on Atoms and Molecules Near Surfaces. (pp. 70 - 73). IOP Publishing LTD Green and gold open access
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Lomas, DA; Belorgey, D; Mallya, M; Miranda, E; Kinghorn, KJ; Sharp, LK; ... Crowther, DC; + view all (2005) Molecular mousetraps and the serpinopathies. BIOCHEMICAL SOCIETY TRANSACTIONS , 33 321 - 330.

Lomas, DA; Belorgey, D; Mallya, M; Miranda, E; Kinghorn, KJ; Sharp, LK; ... Crowther, DC; + view all (2005) Molecular mousetraps and the serpinopathies. Biochem Soc Trans , 33 (Pt 2) 321 - 330. 10.1042/BST0330321.

M

Maretzky, T; Reiss, K; Ludwig, A; Buchholz, J; Scholz, F; Proksch, E; ... Saftig, P; + view all (2005) ADAM10 mediates E-cadherin shedding and regulates epithelial cell-cell adhesion, migration, and beta-catenin translocation. Proc Natl Acad Sci U S A , 102 (26) 9182 - 9187. 10.1073/pnas.0500918102.

Marler, K.J.M.; Kozma, R.; Ahmed, S.; Dong, J.-M.; Hall, C.; Lim, L.; (2005) Outgrowth of neurites from NIE-115 neuroblastoma cells Is prevented on repulsive substrates through the action of PAK. Molecular and Cellular Biology , 25 (12) pp. 5226-5241. 10.1128/MCB.25.12.5226-5241.2005.

Martinez, M; Brice, A; Dürr, A; Vaughan, JR; Zimprich, A; Gasser, T; ... Warter, JM; + view all (2005) Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease. American Journal of Medical Genetics - Neuropsychiatric Genetics , 136 B (1) 72 - 74. 10.1002/ajmg.b.30196.

Martinez, M; Brice, A; Vaughan, JR; Zimprich, A; Breteler, MMB; Meco, G; ... French Parkinson's Disease,; + view all (2005) Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease. AM J MED GENET B , 136B (1) 72 - 74. 10.1002/ajmg.b.30196.

McGowan, E; Pickford, F; Kim, J; Onstead, L; Eriksen, J; Yu, C; ... Golde, T; + view all (2005) A beta 42 is essential for parenchymal and vascular amyloid deposition in mice. NEURON , 47 (2) 191 - 199. 10.1016/j.neuron.2005.06.030.

McInerney-Leo, A; Hadley, DW; Gwinn-Hardy, K; Hardy, J; (2005) Genetic testing in Parkinson's disease. MOVEMENT DISORDERS , 20 (1) 1 - 10. 10.1002/mds.20316.

McKeith, IG; Dickson, DW; Lowe, J; Emre, M; O'Brien, JT; Feldman, H; ... Consortium DLB,; + view all (2005) Diagnosis and management of dementia with Lewy bodies - Third report of the DLB consortium. NEUROLOGY , 65 (12) 1863 - 1872.

McKeon, A; Murphy, S; McNamara, B; Ryder, DQ; Galvin, RJ; (2005) Isolated hypoglossal nerve palsy due to compression by a dissecting vertebral artery. European Neurology , 53 162 - 164.

Meschia, JF; Brott, TG; Brown, RD; Crook, R; Worrall, BB; Kissela, B; ... Investigators, MSGD; + view all (2005) Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke. ANNALS OF NEUROLOGY , 58 (3) 351 - 361. 10.1002/ana.20585.

Meschia, JF; Brott, TG; Brown, RD; Kissela, BM; Hardy, JA; Brown, WM; ... Inv, SISS; + view all (2005) Correlation of proband and sibling stroke latency: The SWISS Study. NEUROLOGY , 64 (6) 1061 - 1063.

Miller, DW; Crawley, A; Gwinn-Hardy, K; Lopez, G; Nussbaum, R; Cookson, MR; ... Dogu, O; + view all (2005) Unaltered alpha-synuclein blood levels in juvenile Parkinsonism with a parkin exon 4 deletion. NEUROSCIENCE LETTERS , 374 (3) 189 - 191. 10.1016/j.neulet.2004.10.053.

Mills, P.B.; Surtees, R.A.H.; Champion, M.P.; Beesley, C.E.; Dalton, N.; Scambler, P.J.; ... Clayton, P.T.; + view all (2005) Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5'-phosphate oxidase. Human Molecular Genetics , 14 (8) pp. 1077-1086. 10.1093/hmg/ddi120.

Misbahuddin, A; Placzek, MR; Taanman, JW; Gschmeissner, S; Schiavo, G; Cooper, JM; Warner, TT; (2005) Mutant torsinA, which causes early-onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH-SY5Y cells. MOVEMENT DISORD , 20 (4) 432 - 440. 10.1002/mds.20351.

Momeni, P; Lu, CS; Chou, YHW; Chang, HC; Chen, RS; Chen, CC; ... Hardy, J; + view all (2005) Taiwanese cases of SCA2 are derived from a single founder. MOVEMENT DISORDERS , 20 (12) 1633 - 1636. 10.1002/mds.20638.

Montiel, R; Bettencourt, C; Silva, C; Santos, C; Prata, MJ; Lima, M; (2005) Analysis of Y-chromosome Variability and its Comparison with mtDNA Variability Reveals Different Demographic Histories Between Islands in the Azores Archipelago (Portugal). Annals of Human Genetics , 69 (2) 135 - 144. 10.1046/j.1469-1809.2004.00146.x.

Morgadinho, AS; Bras, JM; Guerreiro, R; Garrucho, MH; Januario, C; Oliveira, C; Cunha, L; (2005) Parkinson's disease and apolipoprotein E genotype: Possible association? In: MOVEMENT DISORDERS. (pp. S145 - S145). WILEY-LISS

Morris, HR; Wood, NW; Lees, AJ; (2005) Progressive supranuclear palsy (Steele-Richardson-Olszewski disease). In: Morris, H, (ed.) Neurology update: reviews for continuing professional development. (185 - 196). Radcliffe Publishing: Oxford.

Murphy, RT; Mogensen, J; McGarry, K; Bahl, A; Evans, A; Osman, E; ... McKenna, WJ; + view all (2005) Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome - Natural history. J AM COLL CARDIOL , 45 (6) 922 - 930. 10.1016/j.jacc.2004.11.053.

Myers, AJ; Kaleem, M; Marlowe, L; Fung, HC; Duckworth, J; Leung, D; ... Morris, CM; + view all (2005) The H1c haplotype at the MAPT locus is associated with Alzheimer's disease. Human Molecular Genetics , 14 (16) 2399 - 2404. 10.1093/hmg/ddi241.

Myers, AJ; Kaleem, M; Marlowe, L; Pittman, AM; Lees, AJ; Fung, HC; ... Hardy, J; + view all (2005) The H1c haplotype at the MAPT locus is associated with Alzheimer's disease. HUM MOL GENET , 14 (16) 2399 - 2404. 10.1093/hmg/ddi241.

Myers, AJ; Pittman, A; Fung, HC; Kaleem, M; Marlowe, L; Pittman, A; ... Hardy, JA; + view all (2005) The H1c haplotype of the MAPT locus is associated with autopsy confirmed late onset Alzheimer's disease. In: ANNALS OF NEUROLOGY. (pp. ? - ?). WILEY-LISS

Myllykangas, L; Wavrant-De Vrieze, F; Polvikoski, T; Notkola, IL; Sulkava, R; Niinisto, L; ... Tienari, PJ; + view all (2005) Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: A two-stage study. JOURNAL OF THE NEUROLOGICAL SCIENCES , 236 (1-2) 17 - 24. 10.1016/j.jns.2005.04.008.

N

Nagga, K; Garcia, J; Zetterberg, H; Blennow, K; Gottfries, J; Marcusson, J; (2005) Evaluation of factors of importance for clinical dementia diagnosis. Dement Geriatr Cogn Disord , 19 (5-6) 289 - 298. 10.1159/000084554.

Nakaya, Y; Yamane, T; Shiraishi, H; Wang, HQ; Matsubara, E; Sato, T; ... Nishimura, M; + view all (2005) Random mutagenesis of presenilin-1 identifies novel mutants exclusively generating long amyloid beta-peptides. J Biol Chem , 280 (19) 19070 - 19077. 10.1074/jbc.M501130200.

Neumann, M; Mittelbronn, M; Simon, P; Vanmassenhove, B; de Silva, R; Lees, A; ... Kretzschmar, HA; + view all (2005) A New family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects. NEUROPATH APPL NEURO , 31 (4) 362 - 373. 10.1111/j.1365-2990.2005.00629.x.

Nichols, WC; Pankratz, N; Hernandez, D; Paisan-Ruiz, C; Jain, S; Halter, CA; ... Parkinson Study Grp PROGENI Invest,; + view all (2005) Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. LANCET , 365 (9457) 410 - 412.

Nowotny, P; Hinrichs, AL; Smemo, S; Kauwe, JSK; Maxwell, T; Holmans, P; ... Goate, A; + view all (2005) Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 136B (1) 62 - 68. 10.1002/ajmg.b.30186.

O

Ozawa, T; Paviour, D; Quinn, NP; Lees, AJ; Josephs, KA; Healy, DG; ... Revesz, T; + view all (2005) The spectrum of pathological involvement of multiple system atrophy (MSA): clinicopathological correlations. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 244 - 244). BLACKWELL PUBLISHING LTD

Ozawa, T; Paviour, D; Quinn, NP; Revesz, T; Holton, JL; Lees, AJ; (2005) The pathological basis of disproportionate antecollis in multiple system atrophy. In: MOVEMENT DISORDERS. (pp. S111 - S111). WILEY-LISS

P

Paisan-Ruiz, C; Lang, AE; Kawarai, T; Sato, C; Salehi-Rad, S; Fisman, GK; ... Rogaeva, E; + view all (2005) LRRK2 gene in Parkinson disease - Mutation analysis and case control association study. NEUROLOGY , 65 (5) 696 - 700.

Paisan-Ruiz, C; Saenz, A; de Munain, AL; Marti, I; Gil, AM; Marti-Masso, JF; Perez-Tur, J; (2005) Familial Parkinson's disease: Clinical and genetic analysis of four Basque families. ANN NEUROL , 57 (3) 365 - 372. 10.1002/ana.20391.

Papapetropoulos, S; Scaravilli, T; Morris, H; An, SF; Henderson, DC; Quinn, NP; ... Bhatia, KP; + view all (2005) Young onset limb spasticity with PSP-like brain and spinal cord NFT-tau pathology. NEUROLOGY , 64 (4) 731 - 733.

Paviour, DC; Lees, AJ; Josephs, KA; Ozawa, T; Ganguly, M; Strand, C; ... Holton, JL; + view all (2005) Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes presenting with the clinical phenotype of progressive supranuclear palsy (PSP). In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 243 - 243). BLACKWELL PUBLISHING LTD

Paviour, DC; Revesz, T; Holton, JL; Evans, A; Lees, AJ; (2005) Neuronal intranuclear inclusion disease: Report on a case originally diagnosed as dopa-responsive dystonia with Lewy bodies. MOVEMENT DISORD , 20 (10) 1345 - 1349. 10.1002/mds.20559.

Piao, YS; Tan, CF; Iwanaga, K; Kakita, A; Takano, H; Nishizawa, M; ... Takahashi, H; + view all (2005) Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease. ACTA NEUROPATHOL , 110 (6) 600 - 609. 10.1007/s00401-005-1086-5.

Pittman, AM; Myers, A; Fung, HC; Hardy, J; Lees, A; de Silva, R; (2005) Linkage disequilibrium fine-mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degenerarion. In: MOVEMENT DISORDERS. (pp. S35 - S35). WILEY-LISS

Pittman, AM; Myers, AJ; Abou-Sleiman, P; Fung, HC; Kaleem, M; Marlowe, L; ... de Silva, R; + view all (2005) Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration. J MED GENET , 42 (11) 837 - 846. 10.1136/jmg.2005.031377. Gold open access

Plattner, F; Angelo, M; Ris, L; Strand, C; Revesz, T; Holton, JL; Giese, KP; (2005) Age-dependent alterations in tau hyperphosphorylation, APP processing and inhibition of GSK3 mediated by Cdk5 activity. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 221 - 221). BLACKWELL PUBLISHING LTD

Prestel, J; Sharma, M; Leitner, P; Zimprich, A; Vaughan, JR; Durr, A; ... GSPD,; + view all (2005) PARK11 is not linked with Parkinson's disease in European families. EUR J HUM GENET , 13 (2) 193 - 197. 10.1038/sj.ejhg.5201317.

Proukakis, C; Cooper, JM; Taanman, JW; Warner, TT; (2005) Cellular studies of spastin reveal no gain of function, and suggest translation from the 2nd ATG. EUR J NEUROL , 12 323 - 323.

Pulkes, T; Liolitsa, D; Eunson, LH; Rose, M; Nelson, IP; Rahman, S; ... Hanna, MG; + view all (2005) New phenotypic diversity associated with the mitochondrial tRNA (Ser(UCN)) gene mutation. NEUROMUSCULAR DISORD , 15 (5) 364 - 371. 10.1016/j.nmd.2005.01.006.

Pulkes, T; Liolitsa, D; Wills, AJ; Hargreaves, I; Heales, S; Hanna, MG; (2005) Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance. NEUROLOGY , 64 (6) 1091 - 1092.

R

Rüetschi, U; Rosén, A; Karlsson, G; Zetterberg, H; Rymo, L; Hagberg, H; Jacobsson, B; (2005) Proteomic analysis using protein chips to detect biomarkers in cervical and amniotic fluid in women with intra-amniotic inflammation. J Proteome Res , 4 (6) 2236 - 2242. 10.1021/pr050139e.

Rüetschi, U; Zetterberg, H; Podust, VN; Gottfries, J; Li, S; Hviid Simonsen, A; ... Blennow, K; + view all (2005) Identification of CSF biomarkers for frontotemporal dementia using SELDI-TOF. Exp Neurol , 196 (2) 273 - 281. 10.1016/j.expneurol.2005.08.002.

Reed, JA; Wilkinson, PA; Patel, H; Simpson, MA; Chatonnet, A; Robay, D; ... Warner, TT; + view all (2005) A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia. NEUROGENETICS , 6 (2) 79 - 84. 10.1007/s10048-004-0209-9.

Reiman, EM; Chen, KW; Alexander, GE; Caselli, RJ; Bandy, D; Osborne, D; ... Hardy, J; + view all (2005) Correlations between apolipoprotein E epsilon 4 gene dose and brain-imaging measurements of regional hypometabolism. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , 102 (23) 8299 - 8302. 10.1073/pnas.0500579102.

Reinhard, C; Hébert, SS; De Strooper, B; (2005) The amyloid-beta precursor protein: integrating structure with biological function. EMBO J , 24 (23) 3996 - 4006. 10.1038/sj.emboj.7600860.

Reiss, K; Maretzky, T; Ludwig, A; Tousseyn, T; de Strooper, B; Hartmann, D; Saftig, P; (2005) ADAM10 cleavage of N-cadherin and regulation of cell-cell adhesion and beta-catenin nuclear signalling. EMBO J , 24 (4) 742 - 752. 10.1038/sj.emboj.7600548.

Reiss, K; Maretzky, T; Ludwig, A; Tousseyn, T; De Strooper, B; Hartmann, D; Saftig, P; (2005) Erratum: ADAM10 cleavage of N-cadherin and regulation of cell-cell adhesion and β-catenin nuclear signalling (The EMBO Journal (2005) 24 (742-752)). EMBO Journal , 24 (9) 1762 - 1762. 10.1038/sj.emboj.7600671.

Rezai-Zadeh, K; Shytle, D; Sun, N; Mori, T; Hou, HY; Jeanniton, D; ... Tan, J; + view all (2005) Green tea epigallocatechin-3-gallate (EGCG) modulates amyloid precursor protein cleavage and reduces cerebral amyloidosis in Alzheimer transgenic mice. JOURNAL OF NEUROSCIENCE , 25 (38) 8807 - 8814. 10.1523/JNEUROSCI.1521-05.2005. Green open access
file

Rossor, MN; Hanna, MG; (2005) New year... Journal of Neurology, Neurosurgery and Psychiatry , 76 (1) 1 - 1. 10.1136/jnnp.2004.048926.

Rostagno, A; Tomidokoro, Y; Lashley, T; Ng, D; Plant, G; Holton, J; ... Ghiso, J; + view all (2005) Chromosome 13 dementias. CELL MOL LIFE SCI , 62 (16) 1814 - 1825. 10.1007/s00018-005-5092-5.

S

Salehi, M; Houlden, H; Sheikh, A; Poretsky, L; (2005) The diagnosis of adrenal insufficiency in a patient with Allgrove syndrome and a novel mutation in the ALADIN gene. METABOLISM , 54 (2) 200 - 205. 10.1016/j.metabol.2004.08.013.

Salinas, S; Carazo-Salas, RE; Proukakis, C; Cooper, JM; Weston, AE; Schiavo, G; Warner, TT; (2005) Human spastin has multiple microtubule-related functions. J NEUROCHEM , 95 (5) 1411 - 1420. 10.1111/j.1471-4159.2005.03472.x.

Santos, C; Montiel, R; Sierra, B; Bettencourt, C; Fernandez, E; Alvarez, L; ... Aluja, MP; + view all (2005) Understanding differences between phylogenetic and pedigree-derived mtDNA mutation rate: A model using families from the Azores Islands (Portugal). MOL BIOL EVOL , 22 (6) 1490 - 1505. 10.1093/molbev-msi141.

Schott, JM; Warren, JD; Fox, NC; Thom, M; Revesz, T; Scaravilli, F; ... Rossor, MN; + view all (2005) Brain biopsy in dementia: A review of 90 consecutive cases from Queen Square. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 1317 - 1317). B M J PUBLISHING GROUP

Serneels, L; Dejaegere, T; Craessaerts, K; Horré, K; Jorissen, E; Tousseyn, T; ... De Strooper, B; + view all (2005) Differential contribution of the three Aph1 genes to gamma-secretase activity in vivo. Proc Natl Acad Sci U S A , 102 (5) 1719 - 1724. 10.1073/pnas.0408901102.

Silveira-Moriyama, L; Evans, AH; Katzenschlager, R; Lees, AJ; (2005) Correlation between punding and dyskinesias in Parkinson's disease (PD). In: MOVEMENT DISORDERS. (pp. S133 - S133). WILEY-LISS

Silveira-Moriyama, L; Goncalves, LR; Chien, HF; Barbosa, ER; (2005) Botulinum toxin a in the treatment of blepharospasm - A 10-year experience. ARQ NEURO-PSIQUIAT , 63 (2A) 221 - 224. 10.1590/S0004-282X2005000200006. Green and gold open access
file

Silveira-Moriyama, L; Williams, D; Katzenschlager, R; Lees, AJ; (2005) Pizza, mint, and licorice: Smell testing in Parkinson's disease in a UK population. In: MOVEMENT DISORDERS. (pp. S139 - S139). WILEY-LISS

Sinclair, CDJ; Curtis, EA; Garcia, IL; Retter, JA; Hall, BV; Eriksson, S; ... Hinds, EA; + view all (2005) Bose-Einstein Condensation on a Permanent-Magnet Atom Chip. Phys. Rev. A , 72 031603 - ?. 10.1088/1742-6596/19/1/012.

Sinclair, CDJ; Curtis, EA; Garcia, IL; Retter, JA; Hall, BV; Eriksson, S; ... Hinds, EA; + view all (2005) Bose-Einstein condensation on a permanent-magnet atom chip. PHYS REV A , 72 (3) , Article 031603. 10.1103/PhysRevA.72.031603.

Sinclair, CDJ; Curtis, EA; Retter, JA; Hall, BV; Garcia, IL; Eriksson, S; ... Hinds, EA; + view all (2005) Preparation of a Bose-Einstein condensate on a permanent-magnet atom chip. In: Weiner, J and Feenstra, L and Schmiedmayer, J, (eds.) (Proceedings) International Conference on Atoms and Molecules Near Surfaces. (pp. 74 - 77). IOP Publishing LTD Green and gold open access
file

Sinclair, CDJ; Retter, JA; Curtis, EA; Hall, BV; Garcia, IL; Eriksson, S; ... Hinds, EA; + view all (2005) Cold atoms in videotape micro-traps. EUR PHYS J D , 35 (1) 105 - 110. 10.1140/epjd/e2005-00088-6.

Sisodiya, S; Soranzo, N; Wood, NW; Goldstein, DB; (2005) Association of genetic loci: replication or not, that is the question. Neurology , 64 (11) 1989 - ?.

Spadaro, M; Antonini, G; Ursu, S; Lehmann-Horn, F; Jurkat-Rott, K; Veneziano, L; ... Giunti, P; + view all (2005) Erratum: A G301R Na/K-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs (Neurogenetics (2004) 5 (177-185) DOI: org/10.1007/s10048-004-0183-2). Neurogenetics , 6 (3) 169 - 169. 10.1007/s10048-005-0004-2.

Spadaro, M; Ursu, S; Lehmann-Horn, F; Veneziano, L; Antonini, G; Giunti, P; ... Jurkat-Rott, K; + view all (2005) A G301R Na+/K+-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs (vol 5, pg 177, 2004). NEUROGENETICS , 6 (3) 169 - 169. 10.1007/s10048-005-0004-2.

Strand, AD; Aragaki, AK; Shaw, D; Bird, T; Holton, J; Turner, C; ... Olson, JM; + view all (2005) Gene expression in Huntington's disease skeletal muscle: a potential biomarker. HUM MOL GENET , 14 (13) 1863 - 1876. 10.1093/hmg/ddi192.

Strauss, KM; Martins, LM; Plun-Favreau, H; Marx, FP; Kautzmann, S; Berg, D; ... Krüger, R; + view all (2005) Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease. Human Molecular Genetics , 15 (14) 2099 - 2111.

Strauss, KM; Martins, LM; Plun-Favreau, H; Marx, FP; Kautzmann, S; Berg, D; ... Kruger, R; + view all (2005) Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease. HUM MOL GENET , 14 (15) 2099 - 2111. 10.1093/hmg/ddi215.

Stumpf, MPH; Goldstein, DB; Wood, NW; (2005) Introduction: genetic variation and human health. PHILOS T R SOC B , 360 (1460) 1539 - 1541. 10.1098/rstb.2005.1694.

Suarez-Merino, B; Hubank, M; Revesz, T; Harkness, W; Hayward, R; Thompson, D; ... Warr, TJ; + view all (2005) Microarray analysis of pediatric ependymoma identifies a cluster of 112 candidate genes including four transcripts at 22q12.1-q13.3. NEURO-ONCOLOGY , 7 (1) 20 - 31.

Suarez-Merino, B.; Hubank, M.; Revesz, T.; Harkness, W.; Hayward, R.; Thompson, D.; ... Warr, T.J.; + view all (2005) Microarray analysis of pediatric ependymoma identifies a cluster of 112 candidate genes including four transcripts at 22q12.1-q13.3. Neuro-Oncology , 7 (1) pp. 20-31. 10.1215/S1152851704000596. Green open access
file

Sultan, SM; Allen, E; Cooper, RG; Agarwal, S; Oddis, CV; Vencovsky, J; ... Isenberg, DA; + view all (2005) Inter-rater reliability of a new damage assessement tool in patients with idiopathic inflammatory myositis (IIM). In: RHEUMATOLOGY. (pp. I133 - I133). OXFORD UNIV PRESS

Sultan, SM; Allen, E; Kiely, P; Cooper, RG; Oddis, CV; Vencovsky, J; ... Isenberg, DA; + view all (2005) Inter-rater reliability and validity of two disease activity assessment tools in patients with idiopathic inflammatory myositis (IIM). In: RHEUMATOLOGY. (pp. I134 - I134). OXFORD UNIV PRESS

T

Tabrizi, SJ; Blamire, AM; Manners, DN; Rajagopalan, B; Styles, P; Schapira, AHV; Warner, TT; (2005) High-dose creatine therapy for Huntington disease: A 2-year clinical and MRS study. NEUROLOGY , 64 (9) 1655 - 1656.

Tate, S.K.; Depondt, C.; Sisodiya, S.M.; Cavalleri, G.L.; Schorge, S.; Soranzo, N.; ... Goldstein, D.B.; + view all (2005) Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin. Proceedings of the National Academy of Sciences , 102 (15) pp. 5507-5512. 10.1073/pnas.0407346102.

Tate, SK; Depondt, C; Sisodiya, SM; Cavalleri, GL; Schorge, S; Soranzo, N; ... Goldstein, DB; + view all (2005) Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin. P NATL ACAD SCI USA , 102 (15) 5507 - 5512. 10.1073/pnas.0407346102. Gold open access

Tomidokoro, Y; Lashley, T; Rostagno, A; Neubert, TA; Bojsen-Moller, M; Braendgaard, H; ... Ghiso, J; + view all (2005) Familial Danish dementia - Co-existence of Danish and Alzheimer amyloid subunits (ADan and A beta) in the absence of compact plaques. J BIOL CHEM , 280 (44) 36883 - 36894. 10.1074/jbc.M504038200. Gold open access

U

Ule, J; Jensen, K; Mele, A; Darnell, RB; (2005) CLIP: a method for identifying protein-RNA interaction sites in living cells. Methods , 37 (4) 376 - 386. 10.1016/j.ymeth.2005.07.018.

Ule, J; Ule, A; Spencer, J; Williams, A; Hu, JS; Cline, M; ... Darnell, RB; + view all (2005) Nova regulates brain-specific splicing to shape the synapse. Nat Genet , 37 (8) 844 - 852. 10.1038/ng1610.

W

Warner, TT; Cano, SJ; Edwards, M; FitzPatrick, R; Thompson, AJ; Bhatia, KP; (2005) Measuring clinical change in cervical dystonia: A comparison of the CDIP-58 with existing rating scales. In: MOVEMENT DISORDERS. (pp. S23 - S23). WILEY-LISS

Warren, JD; Schott, JM; Fox, NC; Thom, M; Revesz, T; Holton, JL; ... Rossor, MN; + view all (2005) Brain biopsy in dementia. BRAIN , 128 2016 - 2025. 10.1093/brain/awh543.

Whitwell, JL; Josephs, KA; Rossor, MN; Stevens, JM; Revesz, T; Holton, JL; ... Warren, JD; + view all (2005) Magnetic resonance imaging signatures of tissue pathology in frontotemporal dementia. ARCH NEUROL-CHICAGO , 62 (9) 1402 - 1408.

Wilkinson, PA; Simpson, MA; Bastaki, L; Patel, H; Reed, JA; Kalidas, K; ... Crosby, AH; + view all (2005) A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14. J MED GENET , 42 (1) 80 - 82. 10.1136/jmg.2004.020172.

Williams, D.R.; de Silva, R.; Paviour, D.C.; Pittman, A.; Watt, H.C.; Kilford, L.; ... Lees, A.J.; + view all (2005) Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism. Brain , 128 (6) pp. 1247-1258. 10.1093/brain/awh488.

Williams, D.R.; Lees, A.J.; (2005) Visual hallucinations in the diagnosis of idiopathic Parkinson's disease: a retrospective autopsy study. The Lancet Neurology , 4 (10) pp. 605-610. 10.1016/S1474-4422(05)70146-0.

Williams, DR; de Silva, R; Lees, AJ; (2005) Biochemical differences exist between clinical phenotypes of progressive supranuclear palsy: Richardson's syndrome and PSP-Parkinsonism. In: MOVEMENT DISORDERS. (pp. S2 - S3). WILEY-LISS

Williams, DR; de Silva, R; Paviour, DC; Pittman, A; Watt, HC; Kilford, L; ... Lees, AJ; + view all (2005) Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism. BRAIN , 128 1247 - 1258. 10.1093/brain/awh488.

Winters, K; De Keersmaecker, K; Bartic, C; Braeken, D; Borghs, G; De Strooper, B; (2005) Neuronal lithography with single cell resolution on chemically and topographically functionalised surfaces. Proceedings of SPIE - The International Society for Optical Engineering , 5839 410 - 419. 10.1117/12.608208.

Wong, HK; Sakurai, T; Oyama, F; Kaneko, K; Wada, K; Miyazaki, H; ... Nukina, N; + view all (2005) beta Subunits of voltage-gated sodium channels are novel substrates of beta-site amyloid precursor protein-cleaving enzyme (BACE1) and gamma-secretase. J Biol Chem , 280 (24) 23009 - 23017. 10.1074/jbc.M414648200.

Wood, NW; Healy, DG; Depondt, C; Abou-Sleiman, PM; (2005) Commentary on "A genome wide linkage disequilibrium screen in Parkinson's disease" By Foltynie et al. in J Neurol (2005)252:597-602. J NEUROL , 252 (5) 603 - 604. 10.1007/s00415-005-0707-1.

Z

Zetterberg, H; (2005) Increased serum concentrations of intestinal alkaline phosphatase in peritoneal dialysis. Clin Chem , 51 (3) 675 - 676. 10.1373/clinchem.2004.045831.

Zetterberg, H; (2005) Should the MTHFR 1298A>C polymorphism be considered in the clinical evaluation of patients at risk for thrombotic disease? Genet Med , 7 (9) 655 - ?.

Zetterberg, H; Brodsky, MC; Zetterberg, M; (2005) Evolution, exaptation, and stereopsis [1] (multiple letters). Archives of Ophthalmology , 123 (9) 1281 - 1281.

Zetterberg, H; Hammarin, A-L; Nilsson, P; Andersson, E; Lind, B; Blennow, K; (2005) Nya utredningsmöjligheter vid misstänkt Creutzfeldt-Jakobs sjukdom. Likvoranalys av 14-3-3-protein och T-tau/P-tau-kvot ger säkrare diagnos. Lakartidningen , 102 (12-13) 956 - 961.

Zetterberg, H; Hammarin, AL; Nilsson, P; Andersson, E; Lind, B; Blennow, K; (2005) [New investigations in suspected Creutzfeldt-Jakob disease. Analysis of 14-3-3 protein and T-tau in cerebrospinal fluid for safer diagnosis]. Lakartidningen , 102 (12-13) 956 - 961.

Zetterberg, H; Nexö, E; Minthon, L; Boson, R; Regland, B; McCaddon, A; Blennow, KA; (2005) The transcobalamin 776C > G polymorphism may be a modifiable genetic risk factor for Alzheimer's disease. Int Psychogeriatr , 17 (2) 329 - 331.

Zetterberg, H; Zetterberg, M; (2005) Evolution, exaptation, and stereopsis. Arch Ophthalmol , 123 (9) 1281 - ?. 10.1001/archopht.123.9.1281-a.

Zetterberg, M; Tasa, G; Prince, JA; Palmér, M; Juronen, E; Veromann, S; ... Zetterberg, H; + view all (2005) Methylenetetrahydrofolate reductase genetic polymorphisms in patients with cataract. Am J Ophthalmol , 140 (5) 932 - 934. 10.1016/j.ajo.2005.05.026.

This list was generated on Sun Apr 20 04:02:18 2014 BST.