Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation

Autor: K Alner, Gerard R. Ridgway, Nick C. Fox, Tom R. Webb, Sebastien Ourselin, Simon Mead, Jonathan D. Rohrer, H. Hunt, Harpreet Hyare, S Wroe, Matthew J. Clarkson, John Collinge, Peter Rudge, Lisa Cipolotti

Publikováno v: Alner, K, Hyare, H, Mead, S, Rudge, P, Wroe, S, Rohrer, J, Ridgway, G, Ourselin, S, Clarkson, M, Hunt, H, Fox, N C, Webb, T, Collinge, J & Cipolotti, L 2012, ' Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation ', Journal of Neurology, Neurosurgery and Psychiatry, vol. 83, no. 1, pp. 109-114 . https://doi.org/10.1136/jnnp-2011-300167
Journal of Neurology, Neurosurgery and Psychiatry, 83(1), 109-114. BMJ Publishing Group

Background The human prion diseases are a group of universally fatal neurodegenerative disorders associated with the auto-catalytic misfolding of the normal cell surface prion protein (PrP). Mutations causative of inherited human prion disease (IPD)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64a61cc2560a41eb189531eaf92b63c1
https://hdl.handle.net/1871/43249

The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease

Autor: Lisa Cipolotti, John Collinge, R. J. Cordery, K Alner, Martin N. Rossor, A Kennedy, MA Ron

Publikováno v: Journal of neurology, neurosurgery, and psychiatry. 76(3)

Objective: To assess cognitive function in variant Creutzfeldt-Jakob disease (vCJD). We describe the neuropsychological profiles of 10 cases and compare these data with cross sectional data obtained from patients with histologically confirmed sporadi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3534af993498845df747f3f011078627
https://pubmed.ncbi.nlm.nih.gov/15716521

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The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease.

Autor: Cordery RJ; Dementia Research Group, The National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK., Alner K, Cipolotti L, Ron M, Kennedy A, Collinge J, Rossor MN

Publikováno v: Journal of neurology, neurosurgery, and psychiatry [J Neurol Neurosurg Psychiatry] 2005 Mar; Vol. 76 (3), pp. 330-6.