Zobrazeno 1 - 10
of 17
pro vyhledávání: '"William D. Knight"'
Autor:
Sebastian J. Crutch, Riitta Kukkastenvehmas, Dawn Cutler, Elizabeth K. Warrington, Suzie Barker, William D. Knight, Basil H. Ridha, Douglas Jane, Chris Frost, Martin N. Rossor, Norah Epie
Publikováno v:
Alzheimer's & Dementia. 13
Publikováno v:
Knight, W D, Fox, N C, Rossor, M N & Warren, J D 2008, ' The cultural context of visual hallucinations ', Postgraduate Medical Journal, vol. 84, no. 988, pp. 103-105 . https://doi.org/10.1136/pgmj.2007.063727
Postgraduate Medical Journal, 84(988), 103-105. BMJ Publishing Group
Postgraduate Medical Journal, 84(988), 103-105. BMJ Publishing Group
Visual hallucinations (VH) are a cardinal neuropsychiatric symptom and often have important diagnostic implications. The interpretation of VH is influenced by the patient's social and cultural milieu, but the impact of socio-cultural factors on the i
Autor:
Simon Mead, John Beck, J. Kennedy, William D. Knight, John Collinge, Catherine J. Mummery, Martin N. Rossor
Publikováno v:
European Journal of Neurology. 14:829-831
We report the case of a 40 year-old woman who, at 38 years of age, developed insidious memory loss and, subsequently, progressive dementia satisfying criteria for probable Alzheimer's disease (AD) (NINCDS-ADRDA) [Neurology 1984; 34: 939]. Analysis of
Publikováno v:
Journal of the Royal Society of Medicine. 100:252-254
As we move ever closer to the start of August, there remains no sign that the MTAS (Medical Training Application Service) debacle will end. In the months since this sorry episode began, doctors have been united in a way never seen before,1 and the co
Publikováno v:
Neurobiology of Aging, 32(10), 1765-1773. Elsevier Inc.
Knight, W, Kim, L, Douiri, A, Frost, C, Rossor, M & Fox, N C 2011, ' Acceleration of cortical thinning in familial Alzheimer's disease ', Neurobiology of Aging, vol. 32, no. 10, pp. 1765-1773 . https://doi.org/10.1016/j.neurobiolaging.2009.11.013
Knight, W, Kim, L, Douiri, A, Frost, C, Rossor, M & Fox, N C 2011, ' Acceleration of cortical thinning in familial Alzheimer's disease ', Neurobiology of Aging, vol. 32, no. 10, pp. 1765-1773 . https://doi.org/10.1016/j.neurobiolaging.2009.11.013
Background: MRI in presymptomatic autosomal dominant Alzheimer's disease mutation carriers (MC) provides an opportunity to detect changes that pre-date symptoms or clinical diagnosis. We used automated cortical thickness (CTh) measurement to compare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c5f1a0cab2060e27eb12e29e37aeff2
https://research.vumc.nl/en/publications/56e7f333-b730-4e81-8b0d-92bd133a53e8
https://research.vumc.nl/en/publications/56e7f333-b730-4e81-8b0d-92bd133a53e8
Autor:
Nick N. Fox, Matthew J. Clarkson, David J. Brooks, Jonathan W. Bartlett, Ian B. Malone, Martin N. Rossor, Sebastien Ourselin, William D. Knight, Manja Lehmann, Gerard R. Ridgway, A Okello, Natalie S. Ryan, Laura Mancini, John S. Thornton
Publikováno v:
Alzheimer's & Dementia. 6
Background In FAD, 11C-Pittsburgh compound B PET studies have revealed the striatum and thalamus to be the earliest sites of amyloid deposition. We investigated whether these regions also show changes in volume or diffusivity. Methods Twelve Presenil
Autor:
John Hardy, Martin N. Rossor, Daniel McNaughton, Simon Mead, Mark Poulter, William D. Knight, David Nicholl, Rita Guerreiro, Natalie S. Ryan, John Collinge
Publikováno v:
Alzheimer's & Dementia. 5
Autor:
Nick C. Fox, William D. Knight, Jessica Jackson, Lisa Cipolotti, R. Laila Ahsan, Elizabeth K. Warrington, Martin N. Rossor
Publikováno v:
Alzheimer Disease and Associated Disorders, 23(4), 410-414. Lippincott Williams and Wilkins
Knight, W D, Ahsan, R L, Jackson, J, Cipolotti, L, Warrington, E K, Fox, N C I & Rossor, M N 2009, ' Pure Progressive Amnesia and the APPV717G Mutation ', Alzheimer Disease and Associated Disorders, vol. 23, no. 4, pp. 410-414 . https://doi.org/10.1097/WAD.0b013e31819cb7f3
Knight, W D, Ahsan, R L, Jackson, J, Cipolotti, L, Warrington, E K, Fox, N C I & Rossor, M N 2009, ' Pure Progressive Amnesia and the APPV717G Mutation ', Alzheimer Disease and Associated Disorders, vol. 23, no. 4, pp. 410-414 . https://doi.org/10.1097/WAD.0b013e31819cb7f3
We report an isolated, slowly progressive, pure amnestic phenotype in a 59-year-old member of a family affected by autosomal dominant familial Alzheimer disease. Early-onset Alzheimer disease in this family was associated with a V717G mutation in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8808d879fa9841c5ed1382437e33613e
https://research.vumc.nl/en/publications/463c955c-4b5d-42b9-a173-834f15e69b24
https://research.vumc.nl/en/publications/463c955c-4b5d-42b9-a173-834f15e69b24
Autor:
Laila Ahsan, Elizabeth K. Warrington, William D. Knight, Nick C. Fox, Jo Foster, Martin N. Rossor
Publikováno v:
Alzheimer's & Dementia. 4
Autor:
William D. Knight, Martin N. Rossor, Jane E. Warren, Nick C. Fox, Jonathan D. Rohrer, Jason D. Warren
Publikováno v:
Brain, 131(1), 8-38. Oxford University Press
Rohrer, J D, Knight, W D, Warren, J E, Fox, N C, Rossor, M N & Warren, J D 2008, ' Word-finding difficulty: a clinical analysis of the progressive aphasias ', Brain, vol. 131, no. 1, pp. 8-38 . https://doi.org/10.1093/brain/awm251
Rohrer, J D, Knight, W D, Warren, J E, Fox, N C, Rossor, M N & Warren, J D 2008, ' Word-finding difficulty: a clinical analysis of the progressive aphasias ', Brain, vol. 131, no. 1, pp. 8-38 . https://doi.org/10.1093/brain/awm251
The patient with word-finding difficulty presents a common and challenging clinical problem. The complaint of 'word-finding difficulty' covers a wide range of clinical phenomena and may signify any of a number of distinct pathophysiological processes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e44f4c3b5944245ff5168722fb24638
https://research.vumc.nl/en/publications/9f64f28b-5132-43ce-a522-f94ba66a86a0
https://research.vumc.nl/en/publications/9f64f28b-5132-43ce-a522-f94ba66a86a0