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Results: 1-24 |
Results: 24

Authors: Farrer, M Destee, A Levecque, C Singleton, A Engelender, S Becquet, E Mouroux, V Richard, F Defebvre, L Crook, R Hernandez, D Ross, CA Hardy, J Amouyel, P Chartier-Harlin, MC
Citation: M. Farrer et al., Genetic analysis of synphilin-1 in familial Parkinson's disease, NEUROBIOL D, 8(2), 2001, pp. 317-323

Authors: Crook, R Smith, CG Simmons, MY Ritchie, DA
Citation: R. Crook et al., Imaging random telegraph signal sites near a quasi 1D electron system, J PHYS-COND, 13(11), 2001, pp. L249-L254

Authors: Houlden, H Crook, R Dolan, RJ McLaughlin, J Revesz, T Hardy, J
Citation: H. Houlden et al., A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodies, NEUROSCI L, 313(1-2), 2001, pp. 93-95

Authors: Hardy, J Crook, R
Citation: J. Hardy et R. Crook, Presenilin mutations line up along transmembrane alpha-helices, NEUROSCI L, 306(3), 2001, pp. 203-205

Authors: Crook, R
Citation: R. Crook, Making law matter - Rules, rights and security in the lives of the poor - Editorial introduction, IDS BULL, 32(1), 2001, pp. 1-7

Authors: Le, TV Crook, R Hardy, J Dickson, DW
Citation: Tv. Le et al., Cotton wool plaques in non-familial late-onset Alzheimer disease, J NE EXP NE, 60(11), 2001, pp. 1051-1061

Authors: Crook, R Smith, CG Barnes, CHW Simmons, MY Ritchie, DA
Citation: R. Crook et al., Imaging diffraction-limited electronic collimation from a non-equilibrium one-dimensional ballistic constriction, J PHYS-COND, 12(8), 2000, pp. L167-L172

Authors: Crook, R Smith, CG Simmons, MY Ritchie, DA
Citation: R. Crook et al., One-dimensional probability density observed using scanned gate microscopy, J PHYS-COND, 12(50), 2000, pp. L735-L740

Authors: Houlden, H Baker, M McGowan, E Lewis, P Hutton, M Crook, R Wood, NW Kumar-Singh, S Geddes, J Swash, M Scaravilli, F Holton, JL Lashley, T Tomita, T Hashimoto, T Verkkoniemi, A Kalimo, H Somer, M Paetau, A Martin, JJ Van Broeckhoven, C Golde, T Hardy, J Haltia, M Revesz, T
Citation: H. Houlden et al., Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-betaconcentrations, ANN NEUROL, 48(5), 2000, pp. 806-808

Authors: Crook, R Smith, CG Simmons, MY Ritchie, DA
Citation: R. Crook et al., Imaging cyclotron orbits and scattering sites in a high-mobility two-dimensional electron gas, PHYS REV B, 62(8), 2000, pp. 5174-5178

Authors: Myers, A Holmans, P Marshall, H Kwon, J Meyer, D Ramic, D Shears, S Booth, J DeVrieze, FW Crook, R Hamshere, M Abraham, R Tunstall, N Rice, F Carty, S Lillystone, S Kehoe, P Rudrasingham, V Jones, L Lovestone, S Perez-Tur, J Williams, J Owen, MJ Hardy, J Goate, AM
Citation: A. Myers et al., Susceptibility locus for Alzheimer's disease on chromosome 10, SCIENCE, 290(5500), 2000, pp. 2304

Authors: Verkkoniemi, A Somer, M Rinne, JO Myllykangas, L Crook, R Hardy, J Viitanen, M Kalimo, H Haltia, M
Citation: A. Verkkoniemi et al., Variant Alzheimer's disease with spastic paraparesis - Clinical characterization, NEUROLOGY, 54(5), 2000, pp. 1103-1109

Authors: Gwinn-Hardy, KA Crook, R Lincoln, S Adler, CH Caviness, JN Hardy, J Farrer, M
Citation: Ka. Gwinn-hardy et al., A kindred with Parkinson's disease not showing genetic linkage to established loci, NEUROLOGY, 54(2), 2000, pp. 504-507

Authors: Prihar, G Verkkoniemi, A Perez-Tur, J Crook, R Lincoln, S Moulden, H Somer, M Paetau, A Kalimo, H Grover, A Myllykangas, L Hutton, M Hardy, J Haltia, M
Citation: G. Prihar et al., Alzheimer disease PS-1 exon 9 deletion defined, NAT MED, 5(10), 1999, pp. 1090-1090

Authors: Rudrasingham, V Wavrant-De Vrieze, F Lambert, JC Chakraverty, S Kehoe, P Crook, R Amouyel, P Wu, W Rice, F Perez-Tur, J Frigard, B Morris, JC Carty, S Petersen, R Cottel, D Tunstall, N Holmans, P Lovestone, S Chartier-Harlin, MC Goate, A Hardy, J Owen, MJ Williams, J
Citation: V. Rudrasingham et al., alpha-2 macroglobulin gene and Alzheimer disease, NAT GENET, 22(1), 1999, pp. 17-19

Authors: Kehoe, P Wavrant-De Vrieze, F Crook, R Wu, WS Holmans, P Fenton, I Spurlock, G Norton, N Williams, H Williams, N Lovestone, S Perez-Tur, J Hutton, M Chartier-Harlin, MC Shears, S Roehl, K Booth, J Van Voorst, W Ramic, D Williams, J Goate, A Hardy, J Owen, MJ
Citation: P. Kehoe et al., A full genome scan for late onset Alzheimer's disease, HUM MOL GEN, 8(2), 1999, pp. 237-245

Authors: Farrer, M Gwinn-Hardy, K Muenter, M DeVrieze, FW Crook, R Perez-Tur, J Lincoln, S Maraganore, D Adler, C Newman, S MacElwee, K McCarthy, P Miller, C Waters, C Hardy, J
Citation: M. Farrer et al., A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor, HUM MOL GEN, 8(1), 1999, pp. 81-85

Authors: Prihar, G de Chavez, FG Baker, M Crook, R McGowan, E Grover, A Hardy, J Hutton, M
Citation: G. Prihar et al., A novel candidate presenilin-1 interacting protein containing tetratricopeptide repeats, NEUROREPORT, 10(7), 1999, pp. 1409-1415

Authors: Myllykangas, L Polvikoski, T Sulkava, R Verkkoniemi, A Crook, R Tienari, PJ Pusa, AK Niinisto, L O'Brien, P Kontula, K Hardy, J Haltia, M Perez-Tur, J
Citation: L. Myllykangas et al., Genetic association of alpha(2)-macroglobulin with Alzheimer's disease in a Finnish elderly population, ANN NEUROL, 46(3), 1999, pp. 382-390

Authors: Wavrant-DeVrieze, F Lambert, JC Stas, L Crook, R Cottel, D Pasquier, F Frigard, B Lambrechts, M Thiry, E Amouyel, P Tur, JP Chartier-Harlin, MC Hardy, J Van Leuven, F
Citation: F. Wavrant-devrieze et al., Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's disease, HUM GENET, 104(5), 1999, pp. 432-434

Authors: Wavrant-De Vrieze, F Crook, R Holmans, P Kehoe, P Owen, MJ Williams, J Roehl, K Laliiri, DK Shears, S Booth, J Wu, W Goate, A Chartier-Harlin, MC Hardy, J Perez-Tur, J
Citation: F. Wavrant-de Vrieze et al., Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease, NEUROSCI L, 269(2), 1999, pp. 67-70

Authors: Lincoln, S Crook, R Chartier-Harlin, MC Gwinn-Hardy, K Baker, M Mouroux, V Richard, F Becquet, E Amouyel, P Destee, A Hardy, J Farrer, M
Citation: S. Lincoln et al., No pathogenic mutations in the beta-synuclein gene in Parkinson's disease, NEUROSCI L, 269(2), 1999, pp. 107-109

Authors: Wavrant-DeVrieze, F Rudrasingham, V Lambert, JC Chakraverty, S Kehoe, P Crook, R Amouyel, P Wu, W Holmans, P Rice, F Perez-Tur, J Frigard, B Morris, JC Carty, S Cottel, D Tunstall, N Lovestone, S Petersen, RC Chartier-Harlin, MC Goate, A Owen, MJ Williams, J Hardy, J
Citation: F. Wavrant-devrieze et al., No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease, NEUROSCI L, 262(2), 1999, pp. 137-139

Authors: Perez-Tur, J Buee, L Morris, HR Waring, SC Onstead, L Wavrant-De Vrieze, F Crook, R Buee-Scherrer, V Hof, PR Petersen, RC McGeer, PL Delacourte, A Hutton, M Siddique, T Ahlskog, JE Hardy, J Steele, JC
Citation: J. Perez-tur et al., Neurodegenerative diseases of Guam: Analysis of TAU, NEUROLOGY, 53(2), 1999, pp. 411-413
Risultati: 1-24 |