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Number of items: 73.

A

Aguzzi, A and Bitiftler, T and Klein, M and Brandner, S and Raeber, A and Flechsig, E and Weissmann, C (1997) Neurotoxicity and neuroinvasiveness of prions. In: BRAIN PATHOLOGY. (pp. 1137 - 1138). INT SOC NEUROPATHOLOGY

Aguzzi, A and Blattler, T and Klein, MA and Raber, AJ and Hegyi, I and Frigg, R and Brandner, S and Weissmann, C (1997) Tracking prions: The neurografting approach. CELL MOL LIFE SCI , 53 (6) 485 - 495.

Aguzzi, A and Collinge, J (1997) Post-exposure prophylaxis after accidental prion inoculation. LANCET , 350 (9090) 1519 - 1520.

Aguzzi, A and Maddalena, A and Brandner, S and Klein, M (1997) [Molecular pathogenesis of spongiform encephalopathy]. Pathologica , 89 (5) 481 - 490.

Aguzzi, A and Raeber, A and Blattler, T and Flechsig, E and Klein, M and Weissmann, C and Brandner, S (1997) Neurotoxicity and neuroinvasiveness of prions. JOURNAL OF NEUROVIROLOGY , 3 S23 - S24.

B

Baker, M and Kwok, JBJ and Kucera, S and Crook, R and Farrer, M and Houlden, H and Isaacs, A and Lincoln, S and Onstead, L and Hardy, J and Wittenberg, L and Dodd, P and Webb, S and Hayward, N and Tannenberg, T and Andreadis, A and Hallupp, M and Schofield, P and Dark, F and Hutton, M (1997) Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22. ANN NEUROL , 42 (5) 794 - 798.

Ballabio, A and Brown, SDM and Fisher, EMC (1997) Strategies for disease identification. In: Genome Analysis: A laboratory manual. Cold Spring Harbor Laboratory Press: Cold Spring Harbor.

Basun, H and Almkvist, O and Axelman, K and Brun, A and Campbell, TA and Collinge, J and Forsell, C and Froelich, S and Wahlund, LO and Wetterberg, L and Lannfelt, L (1997) Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia. ARCH NEUROL-CHICAGO , 54 (5) 539 - 544.

Blattler, T and Brandner, S and Raeber, AJ and Klein, MA and Voigtlander, T and Weissmann, C and Aguzzi, A (1997) PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brain. NATURE , 389 (6646) 69 - 73.

Bodick, N and Forette, F and Hadler, D and Harvey, RJ and Leber, P and McKeith, IG and Riekkinen, PJ and Rossor, MN and Scheltens, P and Shimohama, S and Spiegel, R and Tanaka, S and Thal, LJ and Urata, Y and Whitehouse, P and Wilcock, G (1997) Protocols to demonstrate slowing of Alzheimer disease progression - Position paper from the International Working Group on Harmonization of Dementia Drug Guidelines. ALZ DIS ASSOC DIS , 11 50 - 53.

Bodick, N and Forette, F and Hadler, D and Harvey, RJ and Leber, P and McKeith, IG and Riekkinen, PJ and Rossor, MN and Scheltens, P and Shimohama, S and Spiegel, R and Tanaka, S and Thal, LJ and Urata, Y and Whitehouse, P and Wilcock, G (1997) Protocols to demonstrate slowing of Alzheimer disease progression. Position paper from the International Working Group on Harmonization of Dementia Drug Guidelines. The Disease Progression Sub-Group. Alzheimer Dis Assoc Disord , 11 Suppl 3 50 - 53.

Budka, H and Hainfellner, JA and Almer, G and BrOcke, T and Windl, O and Kretzschmar, HA and Hill, A and Collinge, J (1997) A new Austrian family with fatal familial insomnia: Brain pathology without detectable PrPres. BRAIN PATHOL , 7 (4) 1267 - 1267.

Budka, H and Hainfellner, JA and Jellinger, K and Kleinert, R and Maier, H and Pilz, P and Sciot, R and Martin, JJ and BojsenMoller, M and Laursen, H and StTeglbjaerg, P and Haltia, M and Kovanen, J and Delisle, MB and Dormont, D and Lasmezas, C and Gray, F and Hauw, JJ and Seilhean, D and Heldt, N and Mikol, J and Vital, C and Foncin, JF and ElHachimi, K and Kopp, N and Bergmann, M and Bilzer, T and CervosNavarro, J and Diringer, H and Feiden, W and Goebel, HH and Bohl, J and Gullotta, F and Jendroska, K and Kretzschmar, HA and Linke, RP and Meyermann, R and Boellaard, JW and Mehraein, P and Schlote, W and Schroder, JM and Schroder, R and Volk, B and Walter, GF and Hori, A and Wiestler, OD and Balloyannis, SJ and Davaki, P and Patsouris, E and Georgsson, G and Farrell, M and Keohane, C and Bugiani, O and Macchi, G and Masullo, C and Costanzi, G and Pocchiari, M and Rizzutto, N and Schiffer, D and Trabattoni, GR and Giangaspero, F and Jansen, GH and Grinde, B and Mork, SJ and Skullerud, K and Lima, C and Pimentel, J and CruzSanchez, FF and Berciano, JA and MartinezLage, J and Navarro, C and Cabello, A and Brun, A and Kristensson, K and Lundberg, PO and Olsson, Y and Collinge, J and Esiri, MM and Graham, D and Ironside, JW and Lantos, PL and MacKenzie, JM and Scaravilli, F and Weller, RO and Will, RG and Allen, IV and Mirakhur, M and Majtenyi, K and Liberski, PP and Petrescu, A and Mitrova, E and Popovic, M and Aguzzi, A and Janzer, RC and Pizzolato, G and Stamm, B and Vandevelde, M and Masters, CL and Tateishi, J and Kitamoto, T and Brown, P (1997) The human prion diseases: from neuropathology to pathobiology and molecular genetics - Final report of an EU Concerted Action. NEUROPATH APPL NEURO , 23 (5) 416 - 422.

C

Colling, SB and Khana, M and Collinge, J and Jefferys, JGR (1997) Mossy fibre reorganization in the hippocampus of prion protein null mice. BRAIN RES , 755 (1) 28 - 35.

Collinge, J (1997) Human prion diseases and bovine spongiform encephalopathy (BSE). HUM MOL GENET , 6 (10) 1699 - 1705.

Collinge, J (1997) Assessing risks of BSE transmission to humans. In: Goebel, K, (ed.) International seminar on nuclear war and planetary emergencies. (54 - 54). World Scientific: Singapore.

Collinge, J and Hill, AF and Ironside, J and Zeidler, M (1997) Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy - Reply. LANCET , 349 (9061) 1323 - 1323.

Collinge, J and Hill, AF and Sidle, KCL and Ironside, J (1997) Biochemical typing of scrapie strains - Reply. NATURE , 386 (6625) 564 - 564.

Collinge, J and Hill, AF and Sidle, KCL and Ironside, J (1997) Typing prion isoforms - Reply. NATURE , 386 (6622) 233 - 234.

Collinge, J and Palmer, MS and Sidle, KCL and Hill, AF and Gowland, I and Meads, J and Asante, E and Bradley, R and Doey, LJ and Lantos, PL (1997) Unaltered susceptibility to BSE in transgenic mice expressing human prion protein (vol 378, pg 779, 1995). NATURE , 389 (6650) 526 - 526.

D

Deslys, JP and Lasmezas, CI and Streichenberger, N and Hill, A and Collinge, J and Dormont, D and Kopp, N (1997) New variant Creutzfeldt-Jakob disease in France. LANCET , 349 (9044) 30 - 31.

Duffner, F and Brandner, S and Opitz, H and Klier, R and Grote, EH (1997) Primary Candida albicans empyema associated with epidural hematomas in craniocervical junction. CLIN NEUROPATHOL , 16 (3) 143 - 146.

E

Esiri, MM and Gordon, WI and Collinge, J and Patten, JS (1997) Peripheral neuropathy in Creutzfeldt-Jakob disease. NEUROLOGY , 48 (3) 784 - 784.

F

Fisher, EMC (1997) The contribution of the mouse to advances in human genetics. Advances in Genetics , 35 155 - 205. 10.1016/S0065-2660(08)60450-2.

Fisher, EMC and Martin, JE (1997) Phenotypic and genotypic characterisation of feeble. In: Neuropathology and Applied Neuropathology.

Fox, NC and Freeborough, PA (1997) Brain atrophy progression measured from registered serial MRI: Validation and application to Alzheimer's disease. J MAGN RESON IMAGING , 7 (6) 1069 - 1075.

Fox, NC and Freeborough, PA and Mekkaoui, KF and Stevens, JM and Rossor, MN (1997) Cerebral and cerebellar atrophy on serial magnetic resonance imaging in an initially symptom free subject at risk of familial prion disease. BRIT MED J , 315 (7112) 856 - 857.

Fox, NC and Kennedy, AM and Harvey, RJ and Lantos, PL and Roques, PK and Collinge, J and Hardy, J and Hutton, M and Stevens, JM and Warrington, EK and Rossor, MN (1997) Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene - Pedigree but not mutation specific age at onset provides evidence for a further genetic factor. BRAIN , 120 491 - 501.

Freeborough, PA and Fox, NC (1997) Measurement of brain volume changes in Alzheimer's disease from registered serial MR scans. Clinical MRI , 7 23 - 26.

Freeborough, PA and Fox, NC (1997) The boundary shift integral: An accurate and robust measure of cerebral volume changes from registered repeat MRI. IEEE T MED IMAGING , 16 (5) 623 - 629.

Freeborough, PA and Fox, NC (1997) Measurement of global and regional cerebral volume changes by integrating boundary shifts between registered serial 3D MR scans. In: Duncan, J and Gindi, G, (eds.) INFORMATION PROCESSING IN MEDICAL IMAGING. (pp. 355 - 368). SPRINGER-VERLAG BERLIN

Freeborough, PA and Fox, NC and Kitney, RI (1997) Interactive algorithms for the segmentation and quantitation of 3-D MRI brain scans. COMPUT METH PROG BIO , 53 (1) 15 - 25.

Fukutani, Y and Cairns, NJ and Rossor, MN and Isaki, K and Lantos, PL (1997) Cerebellar pathology in sporadic and familial Alzheimer's disease: A morphometric investigation. BRAIN PATHOL , 7 (4) 1203 - 1203.

Fukutani, Y and Cairns, NJ and Rossor, MN and Lantos, PL (1997) Cerebellar pathology in sporadic and familial Alzheimer's disease including APP 717 (Val->Ile) mutation cases: A morphometric investigation. J NEUROL SCI , 149 (2) 177 - 184.

G

Green, AJE and Harvey, RJ and Thompson, EJ and Rossor, MN (1997) Increased S100 beta in the cerebrospinal fluid of patients with frontotemporal dementia. NEUROSCI LETT , 235 (1-2) 5 - 8.

H

Harvey, RJ and Summerfield, JA and Fox, NC and Warrington, EK and Rossor, MN (1997) Dementia associated with haemochromatosis: a report of two cases. EUR J NEUROL , 4 (3) 318 - 322.

Hernandez, D and Tybulewicz, V and Fisher, EMC (1997) Modelling aspects of Down syndrome in mice. In: CYTOGENET CELL GENET. (pp. 29 - 29). KARGER

Hill, AF and Desbruslais, M and Joiner, S and Sidle, KCL and Gowland, I and Collinge, J and Doey, LJ and Lantos, P (1997) The same prion strain causes vCJD and BSE. NATURE , 389 (6650) 448 - 450.

Hill, AF and Will, RG and Ironside, J and Collinge, J (1997) Type of prion protein in UK farmers with Creutzfeldt-Jakob disease. LANCET , 350 (9072) 188 - 188.

Hill, AF and Zeidler, M and Ironside, J and Collinge, J (1997) Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy. LANCET , 349 (9045) 99 - 100.

Hoyle, J and Tan, KH and Fisher, EMC (1997) Localization of genes encoding two human one domain members of the AAA family: PSMC5 (the thyroid hormone receptor interacting protein, TRIP1) and PSMC3 (the Tat binding protein, TBP1). Hum Genet , 99 285 - 288.

Hoyle, J and Tan, KH and Fisher, EMC (1997) Mapping human and mouse valosin containing protein (VCP) sequences. Mamm. Genome , 8 778 - 780.

K

Katsanis, N and Beck, JA and Fisher, EMC (1997) Mapping of a novel SH3 domain protein and two proteins of unknown function to human chromosome 21. Hum Genet , 100 477 - 480.

Katsanis, N and Yaspo, M and Fisher, EMC (1997) Identification and mapping of a novel human gene, PRMT2, homologous to the rat protein arginine N-methyltransferase 1 (PRMT1) gene. Mamm Genome , 8 526 - 529.

Khalili-Shirazi, A and Gregson, N and Hughes, R (1997) CD1 expression in human peripheral nerve of GBS patients. Biochem Soc Trans , 25 (2) 172S - ?.

Khalili-Shirazi, A and Gregson, NA and Hall, MA and Hughes, RA and Lanchbury, JS (1997) T cell receptor V beta gene usage in Guillain-Barré syndrome. J Neurol Sci , 145 (2) 169 - 176.

L

Lachmann, P and Allen, I and Anderson, R and Biggs, P and Bostock, C and Collinge, J and Heap, B and Kimberlin, R and Klug, A and Raff, M and Swales, J and Southwood, R and Wilesmith, J and Will, B and Weissman, C (1997) Update on BSE. INTERDISCIPL SCI REV , 22 (3) 181 - 186.

Lantos, PL and Bhatia, K and AlSarraj, S and Doshi, R and Beck, J and Collinge, J (1997) Is the neuropathology of new variant Creutzfeldt-Jakob disease and kuru similar? LANCET , 350 (9072) 187 - 188.

Lantos, PL and Rossor, MN (1997) A prospective clinicopathological study of familial dementias: A neuropathological review of 56 cases. J NEUROPATH EXP NEUR , 56 (5) 136 - 136.

Larner, AJ and Rossor, MN (1997) Alzheimer's disease: Towards therapeutic manipulation of the amyloid precursor protein and amyloid beta-peptides. EXPERT OPIN THER PAT , 7 (10) 1115 - 1127.

Lodi, R and Taylor, DJ and Tabrizi, SJ and Kumar, S and Sweeney, M and Wood, NW and Styles, P and Radda, GK and Schapira, AHV (1997) In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by P-31 magnetic resonance spectroscopy. ANN NEUROL , 42 (4) 573 - 579.

M

Mallucci, GR and Collinge, J (1997) Neuropsychiatric presentations of prion disease. CURR OPIN PSYCHIATR , 10 (1) 59 - 62.

Martin, JE and Fisher, EMC (1997) Phenotypic analysis - making the most of your mouse. Trends Genet. , 13 254 - ?.

Martin, JE and Fisher, EMC and Peters, J and Hunter, J and Brown, SDM and Rogers, D (1997) SHIRPA - Phenotypic assessment of neurological function. In: Neuropathaolgy and Applied Neurobiology.

Mazars, GR and Jat, PS (1997) Expression of p24, a novel p21(Waf1/Cip1/Sdi1)-related protein, correlates with measurement of the finite proliferative potential of rodent embryo fibroblasts. P NATL ACAD SCI USA , 94 (1) 151 - 156.

McGeer, P and Rossor, MN and Bodick, NC (1997) Slowing the progression of Alzheimer disease: Monitoring progression - Discussion. ALZ DIS ASSOC DIS , 11 S9 - S9.

Mileham, P and Fisher, EMC and Neal, L and Peters, J and Martin, JE (1997) Genetic mapping of the gammy (gam) mutation - a putative model of human congenital club foot. In: Neuropathology and Applied Neuropathology.

N

Nickols, CD and Peters, J and Fisher, EMC and Martin, JE (1997) A closer look at the mouse mutant 'gammy' (gam), a proposed model for human club foot. In: Neuropathology and Applied Neuropathology.

Nickols, CK and Peters, J and Fisher, EMC and Martin, JE (1997) Phenotypic analysis of the mouse mutant gammy (gam) and the effects of laterality on scoring in the SHIRPA protocol. In: Beuropathology and Applied Neuropathology.

P

Palmero, I and McConnell, B and Parry, D and Brookes, S and Hara, E and Bates, S and Jat, P and Peters, G (1997) Accumulation of p(16INK4a) in mouse fibroblasts as a function of replicative senescence and not of retinoblastoma gene status. ONCOGENE , 15 (5) 495 - 503.

Piccardo, P and Tagliavini, F and Dlouhy, SR and Young, K and Seiler, C and Rossi, G and Hill, AF and Bugiani, M and Bugiani, O and Langeveld, JPM and Collinge, J and Ghetti, B (1997) Species and disease specific prion protein (PrP) isoforms are detected by antibodies (abs) raised against a highly conserved mid-region sequence. BRAIN PATHOL , 7 (4) 1248 - 1248.

Piccardo, P and Tagliavini, F and Dlouhy, SR and Young, K and Seiler, C and Rossi, G and Hill, AF and Bugiani, O and Collinge, J and Ghetti, B (1997) An antiserum to residues 95-108 of human PrP detects PrPres in a variety of human and animal prion diseases. J NEUROPATH EXP NEUR , 56 (5) 73 - 73.

Post, SG and Beerman, B and Brodaty, H and Gaines, AW and Gauthier, SG and Geldmacher, DS and Hill, S and Homma, A and Rossor, MN and Whitehouse, PJ and Winblad, B (1997) Ethical issues in dementia drug development - Position paper from the International Working Group on Harmonization of Dementia Drug Guidelines. ALZ DIS ASSOC DIS , 11 26 - 28.

R

Raeber, AJ and Race, RE and Brandner, S and Priola, SA and Sailer, A and Bessen, RA and Mucke, L and Manson, J and Aguzzi, A and Oldstone, MBA and Weissmann, C and Chesebro, B (1997) Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie. EMBO J , 16 (20) 6057 - 6065.

Reisberg, B and Burns, A and Brodaty, H and Eastwood, R and Rossor, M and Sartorius, N and Winblad, B (1997) Diagnosis of Alzheimer's disease. Report of an International Psychogeriatric Association Special Meeting Work Group under the cosponsorship of Alzheimer's Disease International, the European Federation of Neurological Societies, the World Health Organization, and the World Psychiatric Association. Int Psychogeriatr , 9 (Suppl 1) 11 - 38. 10.1017/S1041610297004675.

Revesz, T and McLaughlin, JL and Rossor, MN and Lantos, PL (1997) Pathology of familial Alzheimer's disease with Lewy bodies. J NEURAL TRANSM-SUPP (51) 121 - 135.

Rogers, DC and Fisher, EMC and Brown, SDM and Peters, J and Hunter, AJ and Martin, JE (1997) Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment. MAMM GENOME , 8 (10) 711 - 713.

Rossor, MN and Fox, NC and Freeborough, PA and Roques, PK (1997) Slowing the progression of Alzheimer disease: Monitoring progression. ALZHEIMER DISEASE & ASSOCIATED DISORDERS , 11 S6 - S9.

S

Sartorius, N and Rossor, M and Winbald, B and Eastwood, R and Molloy, W and Morris, J (1997) Diagnosis af Alzheimer's disease. Workshop 1: Differential diagnosis. International Psychogeriatrics , 9 (SUPPL. 1) 85 - 86. 10.1017/S1041610297004742.

Sinden, JD and RashidDoubell, F and Kershaw, TR and Nelson, A and Chadwick, A and Jat, PS and Noble, MD and Hodges, H and Gray, JA (1997) Recovery of spatial learning by grafts of a conditionally immortalized hippocampal neuroepithelial cell line into the ischaemia-lesioned hippocampus. NEUROSCIENCE , 81 (3) 599 - 608.

Smith, CJ and Drake, AF and Banfield, BA and Bloomberg, GB and Palmer, MS and Clarke, AR and Collinge, J (1997) Conformational properties of the prion octa-repeat and hydrophobic sequences. FEBS LETT , 405 (3) 378 - 384.

T

Tabrizi, SJ and Cooper, JM and Xuereb, JH and Schapira, AHV (1997) Mechanisms involved in the pathogenesis of Huntington's disease. ANN NEUROL , 42 (3) T202 - T202.

W

Witherden, AS and Nicholson, SJ and Fisher, EMC (1997) The value of mouse mutants. Mouse Genome , 95 856 - 874.

This list was generated on Tue May 21 08:15:41 2013 BST.