Zobrazeno 1 - 9
of 9
pro vyhledávání: '"R. Laila Ahsan"'
Autor:
Randall J. Bateman, John C. Morris, Richard Mayeux, Alison Goate, Andrew J. Saykin, Ian B. Malone, Christopher C. Rowe, Colin L. Masters, Kirsi M. Kinnunen, Clifford R. Jack, Eric McDade, Martin R. Farlow, Stephen Correia, Peter R. Schofield, Daniel S. Marcus, Chris Frost, Paul M. Thompson, Michael Weiner, Reisa A. Sperling, Marc Modat, David M. Cash, Martin N. Rossor, M. Jorge Cardoso, John M. Ringman, Teresa Poole, Nick C. Fox, Sebastien Ourselin, Stephen Salloway, Ralph N. Martins, Kelvin K. Leung, Tammie L.S. Benzinger, Bernardino Ghetti, Jasmeer P. Chhatwal, Adam M. Brickman, R. Laila Ahsan
Publikováno v:
Alzheimer's & Dementia. 14:43-53
Introduction Identifying at what point atrophy rates first change in Alzheimer's disease is important for informing design of presymptomatic trials. Methods Serial T1-weighed magnetic resonance imaging scans of 94 participants (28 noncarriers, 66 car
Autor:
Kirsty Macpherson, Nick C. Fox, Ian B. Malone, Henrik Zetterberg, Simon Mead, R. Laila Ahsan, Yuying Liang, Jana Klimova, Philip S.J. Weston, Kaj Blennow, Jonathan M. Schott, Akshay Nair, Hugh G. Pemberton, Teresa Poole, Natalie S. Ryan, Martin N. Rossor, Ronald Druyeh
Publikováno v:
Alzheimer's & Dementia. 13
Autor:
Ian B. Malone, Christopher A. Lane, M. Jorge Cardoso, Emily N. Manning, Lorna Harper, Sebastien Ourselin, Carole H. Sudre, Jonathan M. Schott, R. Laila Ahsan
Publikováno v:
Alzheimer's & Dementia. 13
Autor:
David J. Brooks, Alexander Hammers, R. Laila Ahsan, Federico Turkheimer, Ralph Myers, Louis Lemieux, Samantha L. Free, Ioannis S. Gousias, Helai Habib, Matthias J. Koepp, John S. Duncan, Richard Allom
Publikováno v:
NeuroImage. 38:261-270
The basal ganglia and thalamus are involved in processing all physiological behaviors and affected by many diseases. Accurate localization is a crucial issue in neuroimaging, particularly when working with groups of normalized images in a standard st
Autor:
Fanjul S, Pilar Gómez Garre, R. Laila Ahsan, Nicola Pavese, Alison C. Jones, Lídice Vidal, Justo García de Yébenes, Michio Hirano, Yen F. Tai, Israel Ampuero, David J. Brooks, Jordi Pérez-Tur, A. Fontán, Hernández J, S Cantarero, Janet Hoenicka, Torbjorn Nyggard, Paola Piccini, Ana I. Rojo, Ana Vazquez, Raquel Ros
Publikováno v:
Annals of Neurology. 57:634-641
Progressive supranuclear palsy (PSP) is a disorder of unknown pathogenesis. Familial clusters of PSP have been reported related to mutations of protein tau. We report the linkage of a large Spanish family with typical autosomal dominant PSP to a new
Publikováno v:
Alzheimer's & Dementia. 7
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:
Jonathan D, Rohrer, R Laila, Ahsan, Adrian M, Isaacs, Jorgen E, Nielsen, Leif, Ostergaard, Rachael, Scahill, Jason D, Warren, Martin N, Rossor, Nick C, Fox, Peter, Johannsen
Publikováno v:
Dementia and geriatric cognitive disorders. 27(2)
CHMP2B mutations are a rare cause of familial frontotemporal dementia (FTD). The clinical syndrome is dominated by personality change and behavioural symptoms, but language, memory, calculation and praxis impairments are also seen early in the course
Autor:
Raquel Ros, Pilar Gómez Garre, Michio Hirano, Yen F. Tai, Israel Ampuero, Lídice Vidal, Ana Rojo, Aurora Fontan, Ana Vazquez, Samira Fanjul, Jaime Hernandez, Susana Cantarero, Janet Hoenicka, Alison Jones, R. Laila Ahsan, Nicola Pavese, Paola Piccini, David J. Brooks, Jordi Perez‐Tur, Torbjorn Nyggard
Publikováno v:
Annals of Neurology; May2005, Vol. 57 Issue 5, p634-641, 8p