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Number of items: 74.

A

Aguzzi, A and Klein, MA and Montrasio, F and Pekarik, V and Brandner, S and Furukawa, H and Kaser, P and Rockl, C and Glatzel, M (2000) Prions: Pathogenesis and reverse genetics. MOLECULAR BASIS OF DEMENTIA , 920 140 - 157.

Aguzzi, A and Raeber, AJ and Brandner, S and Frigg, R and Raeber, AJ and Hegyi, I and Rockl, C and Fischer, MB and Pekarik, V and Huber, GF and Musahl, C and Furukawa, H and Glatzel, M and Parizek, P and Klein, MA (2000) Molecular pathology of prion diseases. J PATHOL , 190 65A - 65A.

B

Barrow, PA and Mallucci, G and Collinge, J and Jefferys, JGR (2000) Rescue of a physiological phenotype in mice with ablated PrP gene but expressing a transgene cassette for PrP. J PHYSIOL-LONDON , 523 203P - 204P.

Beck, JA and Lloyd, S and Hafezparast, M and Lennon-Pierce, M and Eppig, JT and Festing, MFW and Fisher, EMC (2000) Genealogies of mouse inbred strains. NAT GENET , 24 (1) 23 - +.

Bell, K and Cairns, NJ and Lantos, PL and Rossor, MN (2000) Immunohistochemistry distinguishes between Pick's disease and corticobasal degeneration. J NEUROL NEUROSUR PS , 69 (6) 835 - 836.

Benninger, Y and Marino, S and Hardegger, R and Weissmann, C and Aguzzi, A and Brandner, S (2000) Differentiation and histological analysis of embryonic stem cell-derived neural transplants in mice. BRAIN PATHOL , 10 (3) 330 - 341.

Brandner, S and Klein, MA and Aguzzi, A (2000) Mechanisms of neuroinvasion by prions: molecular principles and present status of research. SCHWEIZ MED WSCHR , 130 (12) 435 - 442.

Brandner, S and Klein, MA and Frigg, R and Pekarik, V and Parizek, P and Raeber, A and Glatzel, M and Schwarz, P and Rulicke, T and Weissmann, C and Aguzzi, A (2000) Neuroinvasion of prions: insights from mouse models. EXP PHYSIOL , 85 (6) 705 - 712.

Brandner, S and Marine, S and Kielmann, M and Hardegger, R and Fodde, R and Aguzzi, A (2000) The role of the adenomatous polyposis coli (APC) protein in neural differentiation. BRAIN PATHOL , 10 (4) 762 - 762.

Brex, PA and Jenkins, R and Fox, NC and Crum, WR and O'Riordan, JI and Plant, GT and Miller, DH (2000) Detection of ventricular enlargement in patients at the earliest clinical stage of MS. NEUROLOGY , 54 (8) 1689 - 1691.

C

Collinge, J (2000) Human prion diseases. BRAIN PATHOL , 10 (4) 607 - 607.

Collinge, J (2000) Prion diseases. In: Ledingham, JGG and Warrell, DA, (eds.) Concise Oxford textbook of medicine. (1307 - 1311). Oxford University Press: Oxford, UK.

Collinge, J (2000) Creutzfeldt-Jakob disease and other prion diseases. In: O'Brien, JT and Ames, D and Burns, A, (eds.) Dementia. Hodder Arnold: London, UK.

D

Darmon, AJ and Jat, PS (2000) BAP37 and Prohibitin are specifically recognized by an SV40 T antigen antibody. Mol Cell Biol Res Commun , 4 (4) 219 - 223. 10.1006/mcbr.2001.0281.

F

Festing, MFW and Fisher, EMC (2000) Mighty mice - Clarence Little's brainwave gave biomedical researchers their best friend. NATURE , 404 (6780) 815 - 815.

Fox, NC and Cousens, S and Scahill, R and Harvey, RJ and Rossor, MN (2000) Using serial registered brain magnetic resonance imaging to measure disease progression in Alzheimer disease - Power calculations and estimates of sample size to detect treatment effects. ARCH NEUROL-CHICAGO , 57 (3) 339 - 344.

Fox, NC and Jenkins, R and Leary, SM and Stevenson, VL and Losseff, NA and Crum, WR and Harvey, RJ and Rossor, MN and Miller, DH and Thompson, AJ (2000) Progressive cerebral atrophy in MS - A serial study using registered, volumetric MRI. NEUROLOGY , 54 (4) 807 - 812.

Fox, NC and Rossor, MN (2000) Seeing what Alzheimer saw - with magnetic resonance microscopy. NAT MED , 6 (1) 20 - 21.

Fox, NC and Rossor, MN (2000) Seeing what Alzheimer saw--with magnetic resonance microscopy. Nat Med , 6 (1) 20 - 21. 10.1038/71481.

G

Glatzel, M and Klein, MA and Brandner, S and Aguzzi, A (2000) Prions: from neurografts to neuroinvasion. In: ARCHIVES OF VIROLOGY. (pp. 3 - 12). SPRINGER-VERLAG WIEN

Glatzel, M and Klein, MA and Brandner, S and Aguzzi, A (2000) Prions: from neurografts to neuroinvasion. PRION DISEASES 3 - 12.

H

Hartmann, SL and Cash, DM and Galloway, RL (2000) Spatially accurate 3D visualization of medical images during image-guided surgery. In: MEDICAL IMAGING 2000: IMAGE DISPLAY AND VISUALIZATION. (pp. 248 - 258).

Hill, AF and Joiner, S and Linehan, J and Desbruslais, M and Lantos, PL and Collinge, J (2000) Species-barrier-independent prion replication in apparently resistant species. P NATL ACAD SCI USA , 97 (18) 10248 - 10253.

Huisman, TAGM and Brandner, S and Niggli, F and Betts, DR and Boltshauser, E and Martin, E (2000) Malignant rhabdoid tumor of the brain: Quantitative H-1 MR-spectroscopy and cytogenetics. NEUROPEDIATRICS , 31 (3) 159 - 161.

Huisman, TAGM and Brandner, S and Niggli, F and Kacl, G and Willi, UV and Martin, E (2000) Meningeal hemangiopericytoma in childhood. EUR RADIOL , 10 (7) 1073 - 1075.

Hunter, AJ and Hagan, JJ and Rogers, D and Nolan, P and Strivens, M and Peters, J and Brown, SDM and Fisher, EMC and Martin, J (2000) The discovery of novel behavioural phenotypes via a genome wide mutagenesis programme. EUR J NEUROSCI , 12 442 - 442.

I

Isaacs, A and Potter, A and Masih, M and Vizor, L and Oliver, P and Davies, KE and Peters, J and Nolan, P and Martin, JE and Walsh, FS and Brown, SDM and Hunter, AJ (2000) Evaluation of neurological mouse mutants caused by ENU mutagenesis. In: EUR J NEUROSCI. (pp. 171 - 171). BLACKWELL SCIENCE LTD

Isaacs, AM and Davies, KE and Hunter, AJ and Nolan, PM and Vizor, L and Peters, J and Gale, DG and Kelsell, DP and Latham, ID and Chase, JM and Fisher, EMC and Bouzyk, MM and Potter, A and Masih, M and Walsh, FS and Sims, MA and Doncaster, KE and Parsons, CA and Martin, J and Brown, SDM and Rastan, S and Spurr, NK and Gray, IC (2000) Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy. HUM MOL GENET , 9 (12) 1865 - 1871.

J

Jackson, GS and Collinge, J (2000) Prion disease - the propagation of infectious protein topologies. MICROBES INFECT , 2 (12) 1445 - 1449.

Janssen, JC and Hall, M and Fox, NC and Harvey, RJ and Beck, J and Dickinson, A and Campbell, T and Collinge, J and Lantos, PL and Cipolotti, L and Stevens, JM and Rossor, MN (2000) Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation - A clinicopathological study. BRAIN , 123 894 - 907.

Janssen, JC and Lantos, PL and Al-Sarraj, S and Rossor, MN (2000) Thalamic degeneration with negative prion protein immunostaining. J NEUROL , 247 (1) 48 - 51.

Jenkins, R and Fox, NC and Rossor, AM and Harvey, RJ and Rossor, MN (2000) Intracranial volume and Alzheimer disease - Evidence against the cerebral reserve hypothesis. ARCH NEUROL-CHICAGO , 57 (2) 220 - 224.

John, HA and Laffling, AJ and Marrs, J and Baird, A and Jat, PS and Holdstock, NB and Rossdale, PD (2000) Establishment and characterization of equine autonomic ganglion cell lines to enable direct testing of candidate toxins involved in equine dysautonomia (grass sickness). CELL BIOL TOXICOL , 16 (1) 63 - 74.

K

King, A and Rossor, M and Doey, L and Collinge, J and Lantos, P (2000) Phenotypic variations in a familiar prion disease characterised by a 144 base pair insertion in the Prion protein gene. BRAIN PATHOL , 10 (4) 669 - 669.

Krahenbuhl, S and Brandner, S and Kleinle, S and Liechti, S and Straumann, D (2000) Mitochondrial diseases represent a risk factor for valproate-induced fulminant liver failure. LIVER , 20 (4) 346 - 348.

L

Lantos, PL and Reyesz, T and King, A and Cairns, NJ and Morris, HR and Janssen, J and Rossor, MN (2000) Phenotypic variations in frontotemporal dementia caused by exon 10+16 splice site tau mutation. J NEUROPATH EXP NEUR , 59 (5) 445 - 445.

Larner, AJ and Mathias, CJ and Rossor, MN (2000) Antonomic failure preceding dementia with Lewy bodies. J NEUROL , 247 (3) 229 - 231.

Lidington, EA and Rao, RM and Marelli-Berg, F and Jat, P and Haskard, DO and Mason, JC (2000) Establishment and characterisation of a conditionally transformed immortalised murine cardiac endothelial cell line isolated from H2kb-tsA58 transgenic mice. CIRCULATION , 102 (18) 329 - 329.

Lloyd, SE and Onwuazor, ON and Fisher, EMC and Collinge, J (2000) Quantitative trait locus analysis of prion disease incubation time. Presented at: Join Funders Transmissible Spongiform Encephalopathies workshop, Keele, Uk.

M

Mead, S and Beck, J and Dickinson, A and Fisher, EMC and Collinge, J (2000) Examination of the human prion protein-like gene Doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease. NEUROSCI LETT , 290 (2) 117 - 120.

Moosmann, P and Brandner, S and Kleinle, S and Frauchiger, B (2000) Hyperventilation due to mitochondrial myopathy. J ROY SOC MED , 93 (1) 25 - 26.

N

Nicholson, SJ and Witherden, AS and Hafezparast, M and Martin, JE and Fisher, EMC (2000) Mice, the motor system and human motor neuron pathology. Mammalian Genome , 11 (12) 1041 - 1052.

Nolan, PM and Peters, J and Strivens, M and Rogers, D and Hagan, J and Spurr, N and Gray, IC and Vizor, L and Brooker, D and Whitehill, E and Washbourne, R and Hough, T and Greenaway, S and Hewitt, M and Liu, XH and McCormack, S and Pickford, K and Selley, R and Wells, C and Tymowska-Lalanne, Z and Roby, P and Glenister, P and Thornton, C and Thaung, C and Stevenson, JA and Arkell, R and Mburu, P and Hardisty, R and Kiernan, A and Erven, H and Steel, KP and Voegeling, S and Guenet, JL and Nickols, C and Sadri, R and Naase, M and Isaacs, A and Davies, K and Browne, M and Fisher, EMC and Martin, J and Rastan, S and Brown, SDM and Hunter, J (2000) A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse. NAT GENET , 25 (4) 440 - 443.

Nolan, PM and Peters, J and Vizor, L and Strivens, M and Washbourne, R and Hough, T and Wells, C and Glenister, P and Thornton, C and Martin, J and Fisher, E and Rogers, D and Hagan, J and Reavill, C and Gray, I and Wood, J and Spurr, N and Browne, M and Rastan, S and Hunter, J and Brown, SDM (2000) Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource. MAMM GENOME , 11 (7) 500 - 506.

O

Orth, M and Tabrizi, SJ and Schapira, AHV (2000) Sporadic inclusion body myositis not linked to prion protein codon 129 methionine homozygosity. NEUROLOGY , 55 (8) 1235 - 1235.

P

Pickering-Brown, S and Baker, M and Yen, SH and Liu, WK and Hasegawa, M and Cairns, N and Lantos, PL and Rossor, M and Iwatsubo, T and Davies, Y and Allsop, D and Furlong, R and Owen, F and Hardy, J and Mann, D and Hutton, M (2000) Pick's disease is associated with mutations in the tau gene. ANN NEUROL , 48 (6) 859 - 867.

Pickering-Brown, SM and Owen, F and Isaacs, A and Snowden, J and Varma, A and Neary, D and Furlong, R and Daniel, SE and Cairns, NJ and Mann, DM (2000) Apolipoprotein E epsilon 4 allele has no effect on age at onset or duration of disease in cases of frontotemporal dementia with Pick- or microvacuolar-type histology. EXP NEUROL , 163 (2) 452 - 456.

R

Rigby, SP and Schott, JM and Bliss, P and Higgens, CS and Kamm, MA (2000) Dilated stomach and weak muscles. Lancet , 356 (9245) 1898 - ?.

Rossor, MN (2000) Dementia and driving: European national guidelines. EFNS Scientist Panel on Dementia. Eur J Neurol , 7 (6) 745 - ?.

Rossor, MN and EFNS Sci Panel Dementia, (2000) Dementia and driving: European national guidelines. EUR J NEUROL , 7 (6) 745 - 745.

Rossor, MN and Fox, NC (2000) Mere forgetfulness or early Alzheimer's disease? ANN NEUROL , 47 (4) 419 - 420.

Rossor, MN and Fox, NC (2000) Where in the brain does Alzheimer's disease begin? Annals of Neurology , 47 (4) 421 - 421.

Rossor, MN and Revesz, T and Lantos, PL and Warrington, EK (2000) Semantic dementia with ubiquitin-positive tau-negative inclusion bodies. BRAIN , 123 267 - 276.

S

Sauer, S and Lechner, D and Berlin, K and Lehrach, H and Escary, JL and Fox, NC and Glynn Gut, I (2000) A novel procedure for efficient genotyping of single nucleotide polymorphisms. Nucleic Acids Research , 28 (5) i - viii.
An open access publication

Scaravilli, F and Cordery, RJ and Kretzschmar, H and Gambetti, P and Brink, B and Fritz, V and Temlett, J and Kaplan, C and Fish, D and An, SF and Schulz-Schaeffer, WJ and Rossor, MN (2000) Sporadic fatal insomnia: A case study. ANN NEUROL , 48 (4) 665 - 668.

Scaravilli, F and Kretschmar, H and Gambetti, P and Brink, B and An, SF and Schulz-Schaeffer, WJ and Rossor, MN (2000) Sporadic fatal insomnia (sFI): Report of a case. J NEUROPATH EXP NEUR , 59 (5) 433 - 433.

Selai, CE and Trimble, MR and Rossor, MN and Harvey, RJ (2000) The Quality of Life Assessment Schedule (QOLAS): a new method for assessing quality of life (QOL) in dementia. In: Albert, SM and Logsdon, RG, (eds.) Assessing quality of life in Alzheimer's disease. (31 - 48). Springer Publishing Company: New York.

Sinden, JD and Pilcher, HR and Mann, VM and Kershaw, TR and Dong, Z and Rodriguez, T and Barnetson, A and Majumdar, S and Weeratunga, N and Price, J and Jat, PS (2000) Human neural stem cells: A comparison of genetic and epigenetic approaches to long-term culturing. EUR J NEUROSCI , 12 245 - 245.

Spillantini, MG and Yoshida, H and Rizzini, C and Lantos, PL and Khan, N and Rossor, MN and Goedert, M and Brown, J (2000) A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies. ANN NEUROL , 48 (6) 939 - 943.

T

Tabrizi, SJ and Orth, M and Wilkinson, JM and Taanman, JW and Warner, TT and Cooper, JM and Schapira, AHV (2000) Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicity. HUM MOL GENET , 9 (18) 2683 - 2689.

Tabrizi, SJ and Workman, J and Hart, PE and Mangiarini, L and Mahal, A and Bates, G and Cooper, JM and Schapira, AHV (2000) Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouse. ANN NEUROL , 47 (1) 80 - 86.

Thomas, NJ and Morris, CM and Scaravilli, F and Johansson, J and Rossor, M and De Lange, R and St Clair, D and Nicoll, J and Blank, C and Coulthard, A and Bushby, K and Ince, PG and Burn, D and Kalaria, RN (2000) Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British families. Ann N Y Acad Sci , 903 293 - 298.

V

von Gunten, A and Fox, NC and Cipolotti, L and Ron, MA (2000) A volumetric study of hippocampus and amygdala in depressed patients with subjective memory problems. J NEUROPSYCH CLIN N , 12 (4) 493 - 498.

W

Waldemar, G and Dubois, B and Emre, M and Scheltens, P and Tariska, P and Rossor, M (2000) Diagnosis and management of Alzheimer's disease and other disorders associated with dementia. The role of neurologists in Europe. European Journal of Neurology , 7 (2) 133 - 144.

Waldemar, G and Dubois, B and Emre, M and Scheltens, P and Tariska, P and Rossor, M (2000) Diagnosis and management of Alzheimer's disease and other disorders associated with dementia. The role of neurologists in Europe. European Federation of Neurological Societies. Eur J Neurol , 7 (2) 133 - 144.

Wang, T and Sharma, SD and Fox, N and Rossor, M and Brown, MJ and Sharma, P (2000) Description of a simple test for CADASIL disease and determination of mutation frequencies in sporadic ischaemic stroke and dementia patients. J NEUROL NEUROSUR PS , 69 (5) 652 - 654.

Warren, JD and Chatterton, B and Thompson, PD (2000) A SPECT study of the anatomy of transient global amnesia. Journal of Clinical Neuroscience , 7 57 - 59.

Warren, JD and Kneebone, CS (2000) Facial movement and expression disorders. Part 1. Facial weakness. Medicine Today , 1 (4) 48 - 58.

Warren, JD and Kneebone, CS (2000) Facial movement and expression disorders. Part 2. Excessive movement. Medicine Today , 1 (5) 37 - 40.

Warren, JD and Smith, H and Denson, LA and Waddy, HM (2000) Expressive language disorder after infarction of left lentiform nucleus. Journal of Clinical Neuroscience , 7 456 - 458.

Warren, JD and Thompson, PD (2000) Diencephalic amnesia and apraxia after left thalamic infarction. Journal of Neurology, Neurosurgery and Psychiatry , 68 248 - ?.

Washbourne, R and Nolan, P and Peters, J and Vizor, L and Hewitt, M and Sellley, R and Strivens, M and Martin, J and Fisher, E and Rogers, D and Hagan, J and Spurr, N and Rastan, S and Browne, M and Hunter, J and Brown, S (2000) Identification of novel behavioural mutations using ENU mutagenesis. EUR J NEUROSCI , 12 235 - 235.

Witherden, AS and Nicholson, SJ and Hafezparast, M and Peters, J and Ball, ST and Martin, JE and Rogers, JC and Fisher, EMC (2000) Mapping of Loa, a mouse motor deficit gene, to distal mouse chromosome 12. In: Copp, AJ and Fisher, E, (eds.) Genetics Research.

Z

Zehnder, P and Jenni, W and Brandner, S and Stäubli, M and Waespe, W and Aeschlimann, A (2000) [Vasculitis and mononeuritis multiplex]. Praxis (Bern 1994) , 89 (18) 776 - 784.

This list was generated on Wed Jun 19 04:13:19 2013 BST.