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Brain 2006 129(9):2233-2237; doi:10.1093/brain/awl230
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© The Author (2006). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

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(1) A form of familial presenile dementia with spastic paralysis (including the pathological examination of a case). By C. Worster-Drought, J.G. Greenfield and W.H. McMenemey. Brain 1940: 63; 237–254. Plates VIII–XII. With (2) A form of familial presenile dementia with spastic paralysis. By C. Worster-Drought, J.G. Greenfield and W.H. McMenemey. Brain 1944: 67; 37–43. Plate 1. With (3) Subacute spongiform encephalopathy—a subacute form of encephalopathy attributable to vascular dysfunction (spongiform cerebral atrophy). By S. Nevin, W.H. McMenemey, S. Behrman and D.P Jones (From Maida Vale Hospital for Nervous Diseases and the Brook Hospital, London). Brain 1960: 83; 521–564. Plates LXXIX–LXXXIII. With (4) Creutzfeldt–Jakob disease. The neuropathology of a transmission experiment. By Elisabeth Beck, P.M. Daniel, W.B. Matthews, D.L. Stevens, M.P. Alpers, D.M. Asher, D.C. Gajdusek and C.J. Gibbs Jr (From the Department of Neuropathology, Institute of Psychiatry, The Maudsley Hospital, London, S.E.5, The Derbyshire Royal Infirmary, Derby, and National Institutes . . . [Full Text of this Article]

Alastair Compston

Cambridge


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