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Number of items: 99.

A

Aguzzi, A and Brandner, S and Fischer, MB and Furukawa, H and Glatzel, M and Hawkins, C and Heppner, FL and Montrasio, F and Navarro, B and Parizek, P and Pekarik, V and Prinz, M and Raeber, AJ and Rockl, C and Klein, MA (2001) Spongiform encephalopathies: Insights from transgenic models. ADV VIRUS RES , 56 313 - 352.

Alkadhi, H and Keller, M and Brandner, S and Yonekawa, Y and Kollias, SS (2001) Neuroimaging of cerebellar liponeurocytoma - Case report. J NEUROSURG , 95 (2) 324 - 331.

Asante, EA and Collinge, J (2001) Transgenic studies of the influence of the PrP structure on TSE diseases. ADV PROTEIN CHEM , 57 273 - 311.

B

Beck, JA and Mead, S and Campbell, TA and Dickinson, A and Wientjens, DPMW and Croes, EA and Van Duijn, CM and Collinge, J (2001) Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia. NEUROLOGY , 57 (2) 354 - 356.

Behrens, A and Brandner, S and Genoud, N and Aguzzi, A (2001) Normal neurogenesis and scrapie pathogenesis in neural grafts lacking the prion protein homologue Doppel. EMBO REP , 2 (4) 347 - 352. 10.1093/embo-reports/kve088.

Bigler, ED and Fox, NC and Jenkins, R and Rossor, M (2001) Premorbid brain volume and dementia [1]. Archives of Neurology , 58 (5) 831 - 833.

Brandner, S and Krimpenfort, P and Berns, A and Marino, S (2001) The role of PTEN in cerebellar development and differentiation. ACTA NEUROPATHOL , 102 (5) 520 - 520.

C

Cash, DM and Hartmann, SL and Galloway, RL (2001) Surgically appropriate maximum intensity projections: quantization of vessel depiction and incorporation into surgical navigation. In: MEDICAL IMAGING 2001: VISUALIZATION, DISPLAY, AND IMAGE-GUIDED PROCEDURES. (pp. 221 - 230).

Chakrabarti, L and FReJA, (2001) Clinical and molecular characterisation of frontotemporal dementia linked to human chromosome 3. AMERICAN JOURNAL OF HUMAN GENETICS , 69 (4) 278 - 278.

Chan, D and Crutch, S and Warrington, E (2001) Abnormal colour after images in Alzheimer's disease: a defect of primary visual cortex. J NEUROL NEUROSUR PS , 71 (1) 139 - 139.

Chan, D and Crutch, SJ and Warrington, EK (2001) A disorder of colour perception associated with abnormal colour after-images: a defect of the primary visual cortex. J NEUROL NEUROSUR PS , 71 (4) 515 - 517.

Chan, D and Fox, N and Scahill, R and Crum, W and Whitwell, J and Cipolotti, L and Rossor, MN (2001) Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease. J NEUROL NEUROSUR PS , 70 (2) 276 - 276.

Chan, D and Fox, NC and Jenkins, R and Scahill, RI and Crum, WR and Rossor, MN (2001) Rates of global and regional cerebral atrophy in AD and frontotemporal dementia. NEUROLOGY , 57 (10) 1756 - 1763.

Chan, D and Fox, NC and Scahill, RI and Crum, WR and Whitwell, JL and Leschziner, G and Rossor, AM and Stevens, JM and Cipolotti, L and Rossor, MN (2001) Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease. ANN NEUROL , 49 (4) 433 - 442.

Chan, D. and Fox, N.C. and Scahill, R.I. and Crum, W.R. and Whitwell, J.L. and Leschziner, G. and Rossor, A.M, and Stevens, J.M. and Cipolotti, L. and Rossor, M.N. (2001) Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease. Annals of Neurology , 49 (4) pp. 433-442. 10.1002/ana.92.

Cipolotti, L and Shallice, T and Chan, D and Fox, N and Scahill, R and Harrison, G and Stevens, J and Rudge, P (2001) Long-term retrograde amnesia ... the crucial role of the hippocampus. NEUROPSYCHOLOGIA , 39 (2) 151 - 172.

Clarke, AR and Jackson, GS and Collinge, J (2001) The molecular biology of prion propagation. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES , 356 (1406) 185 - 194.

Collinge, J (2001) Prion diseases of humans and animals: Their causes and molecular basis. ANNU REV NEUROSCI , 24 519 - 550.

Cordery, RJ and Tyrrell, PJ and Lantos, PL and Rossor, MN (2001) Dementia with Lewy bodies studied with positron emission tomography. ARCH NEUROL-CHICAGO , 58 (3) 505 - 508.

Crum, WR and Scahill, RI and Fox, NC (2001) Automated hippocampal segmentation by regional fluid registration of serial MRI: Validation and application in Alzheimer's disease. NEUROIMAGE , 13 (5) 847 - 855.

Crutch, S and Isaacs, R (2001) The significance of an early diagnosis in Alzheimer's disease. CPD Bulletin Old Age Psychiatry , 3 (1) 3 - 5.

Crutch, S.J. and Isaacs, R. and Rossor, M.N. (2001) Some workmen can blame their tools: artistic change in an individual with Alzheimer's disease. The Lancet , 357 (9274) pp. 2129-2133. 10.1016/S0140-6736(00)05187-4.

Crutch, SJ and Isaacs, R and Rossor, MN (2001) Some workmen can blame their tools: artistic change in an individual with Alzheimer's disease. LANCET , 357 (9274) 2129 - 2133.

Crutch, SJ and Warrington, EK (2001) Acalculia: Deficits of operational and quantity number knowledge. J INT NEUROPSYCH SOC , 7 (7) 825 - 834.

Crutch, SJ and Warrington, EK (2001) Refractory dyslexia - Evidence of multiple task-specific phonological output stores. BRAIN , 124 1533 - 1543.

Curtin, JA and Tsipouri, V and Latham, I and Nolan, P and Hardisty, R and Vizor, L and Sims, MA and Parsons, C and Naase, MA and Doncaster, K and Rastan, S and Hunter, AJ and Brown, S and Fisher, EMC and Gray, IC and Spur, NK (2001) Rapid genome scan reveals linkage to chromosome 15 for the ENU induced circling mouse mutant, spin cycle. In: Copp, AJ and Fisher, EMC, (eds.) Genetcis Research. (pp. 203 - ?). Cambridge Journals

D

Darmon, AJ and Jat, PS (2001) Immortalisation of primary rodent cells by SV40. In: UNSPECIFIED (7 - 41).

Donaghy, M and Compston, A and Rossor, M and Warlow, C (2001) Clinical diagnosis. In: Brain's diseases of the nervous system. (1 - 59). Oxford University Press

F

Flechsig, E and Hegyi, I and Enari, M and Schwarz, P and Collinge, J and Weissmann, C (2001) Transmission of scrapie by steel-surface-bound prions. MOL MED , 7 (10) 679 - 684.
An open access publication

Fox, N and Scahill, R and Hogh, P and Rossor, MN (2001) Alzheimer's disease and neuroimaging. In: Dawbarn, D and Allen, SJ, (eds.) Neurobiology of Alzheimer's disease: molecular and cellular neurobiology (Molecular and Cellular Neurobiology Series). (312 - 337). Oxford University Press: Oxford.

Fox, N.C. and Crum, W.R. and Scahill, R.I. and Stevens, J.M. and Janssen, J.C. and Rossor, M.N. (2001) Imaging of onset and progression of Alzheimer's disease with voxel-compression mapping of serial magnetic resonance images. The Lancet , 358 (9277) pp. 201-205. 10.1016/S0140-6736(01)05408-3.

Fox, NC and Crum, WR and Scahill, RI and Stevens, JM and Janssen, JC and Rossor, MN (2001) Imaging of onset and progression of Alzheimer's disease with voxel-compression mapping of serial magnetic resonance images. LANCET , 358 (9277) 201 - 205.

Fox, NC and Jenkins, R and Rossor, M (2001) Premorbid brain volume and dementia - Reply. ARCH NEUROL-CHICAGO , 58 (5) 832 - 833.

G

Gasser, T and Dichgans, M and Finsterer, J and Hausmanowa-Petrusewicz, I and Jurkat-Rott, K and Klopstock, T and LeGuern, E and Lehesjoki, AE and Lehmann-Horn, F and Lynch, T and Morris, H and Rossor, M and Steinlein, OK and Wood, N and Zaremba, J and Zeviani, M and Zoharn, A and EFNS Task Force on Molecular Diagnosis of Neurologic Disorders, (2001) EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. First of two parts. Eur J Neurol , 8 (4) 299 - 314.

Gasser, T and Dichgans, M and Finsterer, J and Hausmanowa-Petrusewicz, I and Jurkat-Rott, K and Klopstock, T and Leguern, E and Lehesjoki, AE and Lehmann-Horn, F and Lynch, T and Morris, H and Rossor, M and Steinlein, OK and Wood, N and Zaremba, J and Zeviani, M and Zoharn, A and EFNS Task Force on Molecular Diagnosis of Neurologic Disorders, (2001) EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. Second of two parts. Eur J Neurol , 8 (5) 407 - 424.

George-Hyslop, PS and Rossor, M (2001) Alzheimer's disease. Unravelling the disease process. Lancet , 358 Suppl S1 - ?.

Glatzel, M and Brandner, S and Klein, MA and Aguzzi, A (2001) Prions: from neurografts to neuroinvasion. Methods Mol Med , 59 129 - 147. 10.1385/1-59259-134-5:129.

Good, CD and Scahill, RI and Fox, NC and Fox, NC and Ashburner, J and Chan, DC and Crum, WR and Rossor, MN and Frackowiak, RSJ (2001) Patterns of cerebral atrophy in Alzheimer's disease and semantic dementia: A comparison of voxel based morphometry and region of interest measurements. NEUROIMAGE , 13 (6) S317 - S317.

H

Harvey, RJ and Rossor, MN (2001) Dementia: trial design and experience with large multicentre trials. In: Guiloff, RJ, (ed.) Clinical trials in neurology. (183 - 198). Springer Verlag: London.

Harvey, RJ and Rossor, MN (2001) Alzheimer's disease and other degenerative dementias. In: Scolding, N, (ed.) Contemporary treatments in neurology. (36 - 58). Butterworth-Heinemann: Oxford.

Hasnain, SS and Murphy, LM and Strange, RW and Grossmann, JG and Clarke, AR and Jackson, GS and Collinge, J (2001) XAFS study of the high-affinity copper-binding site of human PrP91-231 and its low-resolution structure in solution. J MOL BIOL , 311 (3) 467 - 473. 10.1006/jmbi.2001.4795.

Hill, AF and Collinge, J (2001) Strain variations and species barriers. Contrib Microbiol , 7 48 - 57.

Houlden, H and Baker, M and Morris, HR and MacDonald, N and Pickering-Brown, S and Adamson, J and Lees, AJ and Rossor, MN and Quinn, NP and Kertesz, A and Khan, MN and Hardy, J and Lantos, PL and George-Hyslop, PS and Munoz, DG and Mann, D and Lang, AE and Bergeron, C and Bigio, EH and Litvan, I and Bhatia, KP and Dickson, D and Wood, NW and Hutton, M (2001) Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype. NEUROLOGY , 56 (12) 1702 - 1706.

I

Ishii, K and Lippa, C and Tomiyama, T and Miyatake, F and Ozawa, K and Tamaoka, A and Hasegawa, T and Fraser, PE and Shoji, S and Nee, LE and Pollen, DA and St George-Hyslop, PH and Ii, K and Ohtake, T and Kalaria, RN and Rossor, MN and Lantos, PL and Cairns, NJ and Farrer, LA and Mori, H (2001) Distinguishable effects of Presenilin-1 and APP717 mutations on amyloid plaque deposition. NEUROBIOL AGING , 22 (3) 367 - 376.

J

Jackson, GS and Beck, JA and Navarrete, C and Brown, J and Sutton, PM and Contreras, M and Collinge, J (2001) HLA-DQ7 antigen and resistance to variant CJD. Nature , 414 (6861) 269 - 270. 10.1038/35104694.

Jackson, GS and Beck, JA and Navarrete, C and Brown, J and Sutton, PM and Contreras, M and Collinge, J (2001) Pathogenesis - HLA-DQ7 antigen and resistance to variant CJD. NATURE , 414 (6861) 269 - 270.

Jackson, GS and Collinge, J (2001) The molecular pathology of CJD: old and new variants. J CLIN PATHOL-MOL PA , 54 (6) 393 - 399.

Jackson, GS and Murray, I and Hosszu, LLP and Gibbs, N and Waltho, JP and Clarke, AR and Collinge, J (2001) Location and properties of metal-binding sites on the human prion protein. P NATL ACAD SCI USA , 98 (15) 8531 - 8535.

Janssen, JC and Lantos, PL and Fox, NC and Harvey, RJ and Beck, J and Dickinson, A and Campbell, TA and Collinge, J and Hanger, DP and Cipolotti, L and Stevens, JM and Rossor, MN (2001) Autopsy-confirmed familial early-onset Alzheimer disease caused by the L153V presenilin 1 mutation. ARCH NEUROL-CHICAGO , 58 (6) 953 - 958.

Jenkins, R and Fox, NC and Rossor, MN (2001) Rates or global atrophy and sensitivity and specificity in AD. NEUROBIOL AGING , 22 (2) 340 - 341.

Johannsen, P and Gade, A and Brown, J and Chakrabarti, L and Gjedde, A and Gydesen, S and Sorensen, SA and FReJA-Consortium, (2001) Chromosome-3 linked frontotemporal dementia (FTD3) and cerebral blood flow. Presented at: NorAge meeting, Norway.

Jung, HH and Hergersberg, M and Kneifel, S and Alkadhi, H and Schiess, R and Weigell-Weber, M and Brandner, S and Daniels, G and Buck, A and Kollias, S and Hess, K (2001) McLeod syndrome: X-linked choreoacanthocytosis with predominant psychiatric manifestations. J NEUROL NEUROSUR PS , 70 (2) 279 - 279.

Jung, HH and Russo, D and Redman, C and Brandner, S (2001) Kell and XK immunohistochemistry in McLeod myopathy. MUSCLE NERVE , 24 (10) 1346 - 1351.

K

Kennedy, AM and Rossor, MN and Hodges, JR (2001) Familial and sporadic Alzheimer's disease. In: Hodges, JR, (ed.) Early-onset dementia: a multidisciplinary approach. (263 - 283). Oxford University Press: Oxford.

Kulczycki, J and Collinge, J and Lojkowska, W and Parnowski, T and Wierzba-Bobrowicz, T (2001) Report on the first Polish case of the Gerstmann-Straussler-Scheinker syndrome. FOLIA NEUROPATHOL , 39 (1) 27 - 31.

L

Lantos, PL and Khan, N and Cairns, NJ and Janssen, JC and Morris, HR and Rossor, MN (2001) The neuropathological classification of familial frontotemporal dementia. J NEUROPATH EXP NEUR , 60 (5) 513 - 513.

Lidington, EA and Rao, RM and Marelli-Berg, F and Jat, P and Haskard, DO and Mason, JC (2001) Isolation and characterisation of conditionally immortal growth factor responsive cardiac endothelial cells (EC) from H-2K(b)-tsA58 transgenic mice. RHEUMATOLOGY , 40 8 - 8.

Lloyd, S.E. and Onwuazor, O.N. and Beck, J.A. and Mallinson, G. and Farrall, M. and Targonski, P. and Collinge, J. and Fisher, E.M.C. (2001) Identification of multiple quantitative trait loci linked to prion disease incubation period in mice. Proceedings of the National Academy of Sciences , 98 (11) pp. 6279-6283. 10.1073/pnas.101130398.

Lloyd, SE and Onwuazor, ON and Beck, JA and Mallinson, G and Farrall, M and Targonski, P and Collinge, J and Fisher, EMC (2001) Identification of multiple quantitative trait loci linked to prion disease incubation period in mice. P NATL ACAD SCI USA , 98 (11) 6279 - 6283.

M

Mahal, SP and Asante, EA and Antoniou, M and Collinge, J (2001) Isolation and functional characterisation of the promoter region of the human prion protein gene. GENE , 268 (1-2) 105 - 114.

Makrinou, E and Collinge, J and Antoniou, M (2001) Genomic characterisation of the human PRNP/PRND locus. AM J HUM GENET , 69 (4) 369 - 369.

Mann, DMA and Pickering-Brown, SM and Takeuchi, A and Iwatsubo, T and Arango, J and Bird, T and Van Broeckhoven, C and Brooks, W and Brown, R and Cairns, N and Cras, P and Ellison, D and Haltia, M and Ii, K and Jorgensen, A and Krill, J and Lantos, P and Lippa, C and Martins, R and Nochlin, D and Pollen, D and Rosenberg, C and Rossor, M and Tabira, T (2001) Amyloid angiopathy and variability in amyloid β deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease. American Journal of Pathology , 158 (6) 2165 - 2175.

Mann, DMA and Takeuchi, A and Sato, S and Cairns, NJ and Lantos, PL and Rossor, MN and Haltia, M and Kalimo, H and Iwatsubo, T (2001) Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin-1 gene show an unusual but characteristic beta-amyloid pathology known as 'cotton wool' plaques. NEUROPATH APPL NEURO , 27 (3) 189 - 196.

Mason, JC and Lidington, EA and Rao, RM and Marelli-Berg, FM and Jat, PS and Haskard, DO (2001) Use of H-2Kb-tsA58 transgenic mice to generate conditionally immortalized, growth factor responsive mouse cardiac endothelial cells for in vitro studies. FASEB J , 15 (5) A947 - A947.

Masuoka, J and Brandner, S and Paulus, W and Soffer, D and Vital, A and Chimelli, L and Jouvet, A and Yonekawa, Y and Kleihues, P and Ohgaki, H (2001) Germline SDHD mutation in paraganglioma of the spinal cord. ONCOGENE , 20 (36) 5084 - 5086.

Mead, S and Mahal, SP and Beck, J and Campbell, T and Farrall, M and Fisher, E and Collinge, J (2001) Sporadic - but not variant - Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP Exon 1. AM J HUM GENET , 69 (6) 1225 - 1235.

Mead, SH and Mahal, SP and Farrall, M and Fisher, EMC and Collinge, J (2001) Association of prion protein gene single nucleotide polymorphism haplotypes with Creutzfeldt-Jakob disease. AM J HUM GENET , 69 (4) 182 - 182.

Morris, HR and Khan, MN and Janssen, JC and Brown, JM and Perez-Tur, J and Baker, M and Ozansoy, M and Hardy, J and Hutton, M and Wood, NW and Lees, AJ and Revesz, T and Lantos, P and Rossor, MN (2001) The genetic and pathological classification of familial frontotemporal dementia. ARCH NEUROL-CHICAGO , 58 (11) 1813 - 1816.

Murphy, LM and Hasnain, SS and Strange, RW and Grossmann, JG and Clarke, AR and Jackson, GS and Collinge, J (2001) A new copper binding site in N-terminal truncated recombinant human PrP91-231. J INORG BIOCHEM , 86 (1) 351 - 351.

O

O'Brien, JT and Paling, S and Barber, R and Williams, ED and Ballard, C and McKeith, IG and Gholkar, A and Crum, WR and Rossor, MN and Fox, NC (2001) Progressive brain atrophy on serial MRI in dementia with Lewy bodies, AD, and vascular dementia. NEUROLOGY , 56 (10) 1386 - 1388.

O'Doherty, A and Ruf, S and Hernandez, D and Tybulewicz, V and Fisher, EMC (2001) Generation of transchromosomal mice using ES cells containing freely segregating fragments of Hsa21: a model for human Down syndrome. In: Cytogenetics and Cell Genetics.

O'Doherty, A and Ruf, S and Hernandez, D and Tybulewicz, V and Fisher, EMC (2001) Generation of transchromosomal mice using ES cells containing freely segregating fragments of human chromosome 21 (Hsa21): a model of human Down syndrome. In: Copp, AJ and Fisher, EMC, (eds.) Genetics Research. (pp. 200 - ?). Cambridge Journals

O'Hare, MJ and Bond, J and Clarke, C and Takeuchi, Y and Atherton, AJ and Berry, C and Moody, J and Silver, ARJ and Davies, DC and Alsop, AE and Neville, AM and Jat, PS (2001) Conditional immortalization of freshly isolated human mammary fibroblasts and endothelial cells. P NATL ACAD SCI USA , 98 (2) 646 - 651.

P

Pepys, HB and Collinge, J and Barron, LD and Collinge, J and Masel, J and Tahari-Alaoui, A and Lansbury, P and Exley, C and Feizi, T (2001) The molecular biology of prion propagation - Discussion. PHILOS T R SOC B , 356 (1406) 194 - 195.

Pepys, MB and Caughey, B and Kelly, JW and Ellis, RJ and Collinge, J and Perutz, MF and Masel, J (2001) Prion protein interconversions - Discussion. PHILOS T R SOC B , 356 (1406) 200 - 202.

Petersen, RC and Doody, R and Kurz, A and Mohs, RC and Morris, JC and Rabins, PV and Ritchie, K and Rossor, M and Thal, L and Winblad, B (2001) Current concepts in mild cognitive impairment. Arch Neurol , 58 (12) 1985 - 1992.

R

Reis, RM and Herva, R and Brandner, S and Koivukangas, J and Mironov, N and Bar, W and Kleihues, P and Ohgaki, H (2001) Second primary glioblastoma. J NEUROPATH EXP NEUR , 60 (2) 208 - 215.

Rogers, DC and Peters, J and Martin, JE and Ball, S and Nicholson, SJ and Witherden, AS and Hafezparast, M and Latcham, J and Robinson, TL and Quilter, CA and Fisher, EMC (2001) SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice. NEUROSCI LETT , 306 (1-2) 89 - 92.

Rossor, M (2001) Snouting, pouting and rooting. Practical Neurology , 1 (2) 119 - 121.

Rossor, M (2001) Coma. In: Donaghy, M, (ed.) Brain's diseases of the nervous system. (717 - 732). Oxford University Press: Oxford.

Rossor, M (2001) Headache. In: Donaghy, M, (ed.) Brain's diseases of the nervous system. (105 - 123). Oxford University Press: Oxford.

Rossor, M (2001) Neuropsychological disorders, dementia, and behavioural neurology. In: Donaghy, M, (ed.) Brain's diseases of the nervous system. (733 - 774). Oxford University Press: Oxford.

Rossor, MN (2001) Pick's disease: a clinical overview. Neurology , 56(Sup (11) S3 - S5.

Rossor, MN (2001) Pick's disease: A clinical overview. Neurology , 56 (11 SUPPL. 4) S3 - S5.

Rossor, MN (2001) Pick's disease: a clinical overview. Neurology , 56 (11 Suppl 4) S3 - S5.

Rossor, MN (2001) Can the physician predict the neuropathologist? NEUROPATHOLOGY AND GENETICS OF DEMENTIA , 487 1 - 4.

Rossor, MN and Janssen, JC and Fox, NC and Harvey, RJ and Stevens, J and Warrington, EK (2001) Lessons in familial Alzheimer's disease. In: Tanaka, C and McGeer, PL and Ihara, Y, (eds.) UNSPECIFIED (259 - 265). BIRKHAUSER VERLAG AG

S

Sattar, Z and Tayebi, M and Kaisar, M and Khalili-Shirazi, A and Mallinson, G and Jackson, GS and Collinge, J and Hawke, S (2001) PrP conformation and genotype profoundly influence anti-PrP antibody specificity. In: Immunology. (pp. 54 - 54).

Scahill, RI and Crum, WR and Fox, NC (2001) Novel methodology for assessment of progression of hippocampal atrophy from volumetric MR scans. NEUROBIOL AGING , 22 (2) 331 - 332.

Selai, C.E. and Trimble, M.R. and Rossor, M.N. and Harvey, R.J. (2001) Assessing quality of life in dementia: preliminary psychometric testing of the quality of life asessment schedule (QOLAS). Neuropsychological Rehabilitation , 11 (3-4) pp. 219-243. 10.1080/09602010042000033.

Selai, CE and Trimble, MR and Rossor, MN and Harvey, RJ (2001) Assessing quality of life in dementia: Preliminary psychometric testing of the Quality of Life Assessment Schedule (QOLAS). NEUROPSYCHOL REHABIL , 11 (3-4) 219 - 243.

Stevens, JM and Fox, NC (2001) Structural imaging. In: Hodges, JR, (ed.) Early-onset dementia: a multidisciplinary approach. (124 - 141). Oxford University Press: Oxford.

W

Wadsworth, J.D.F. and Joiner, S. and Hill, A.F. and Campbell, T.A. and Desbruslais, M. and Luthert, P.J. and Collinge, J. (2001) Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay. The Lancet , 358 (9277) pp. 171-180. 10.1016/S0140-6736(01)05403-4.

Wadsworth, JDF and Joiner, S and Hill, AF and Campbell, TA and Desbruslais, M and Luthert, PJ and Collinge, J (2001) Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay. LANCET , 358 (9277) 171 - 180.

Walters, RJL and Fox, NC and Crum, WR and Taube, D and Thomas, DJ (2001) Haemodialysis and cerebral oedema. NEPHRON , 87 (2) 143 - 147.

Warren, JD and Kimber, TE and Blumbergs, PC and Thompson, PD (2001) An 89 year old man with generalised chorea and basal ganglia mineralisation. Movement Disorders , 16 362 - 363.

Warrington, EK and Agnew, SK and Kennedy, AM and Rossor, MN (2001) Neuropsychological profiles of familial Alzheimer's disease associated with mutations in the presenilin 1 and amyloid precursor protein genes. J NEUROL , 248 (1) 45 - 50.

Whitwell, JL and Crum, WR and Watt, HC and Fox, NC (2001) Normalization of cerebral volumes by use of intracranial volume: Implications for longitudinal quantitative MR imaging. AM J NEURORADIOL , 22 (8) 1483 - 1489.

Witherden, AS and Hafezparast, M and Nicholson, SJ and Bermingham, NA and Peters, J and Ball, ST and Rogers, DC and Martin, JE and Fisher, EMC (2001) Mapping of Loa, a mouse motor deficit mutation, to distal chromosome 12. In: Copp, AJ and Fisher, EMC, (eds.) Genetics Research. (pp. 203 - ?).

This list was generated on Sun May 19 07:25:58 2013 BST.