Zobrazeno 1 - 10
of 153
pro vyhledávání: '"Zaiwalla, Z."'
Autor:
Barber, T, Muhammed, K, Drew, D, Lawton, M, Crabbe, M, Rolinski, M, Quinnell, T, Zaiwalla, Z, Ben-Shlomo, Y, Husain, M, Hu, M
Publikováno v:
European Journal of Neurology.
Background Apathy is an important neuropsychiatric feature of Parkinson’s disease (PD), which often emerges before the onset of motor symptoms. Patients with rapid eye movement sleep behaviour disorder (RBD) have a high probability of developing Pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2f0798ce3647c2d2d0e2ec4f02f7c301
http://ora.ox.ac.uk/objects/uuid:
http://ora.ox.ac.uk/objects/uuid:
Autor:
Davies, B, Brown, L, Cais, O, Watson, J, Clayton, A, Chang, V, Biggs, D, Preece, C, Hernandez-Pliego, P, Krohn, J, Bhomra, A, Twigg, S, Rimmer, A, Kanapin, A, Consortium, WGS500, Sen, A, Zaiwalla, Z, McVean, G, Foster, R, Donnelly, P, Taylor, J, Blair, E, Nutt, D, Aricescu, A, Greger, I, Peirson, S, Flint, J, Martin, H
Publikováno v:
Human Molecular Genetics. 26(20)
The discovery of genetic variants influencing sleep patterns can shed light on the physiological processes underlying sleep. As part of a large clinical sequencing project, WGS500, we sequenced a family in which the two male children had severe devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::891918c7e5be6ac75cde062c61121df6
http://ora.ox.ac.uk/objects/uuid:
http://ora.ox.ac.uk/objects/uuid:
Autor:
Anand, G., Collett-White, F., Orsini, A., Thomas, S., Jayapal, S., Trump, N., Zaiwalla, Z., Jayawant, S.
Publikováno v:
In European Journal of Paediatric Neurology September 2016 20(5):761-765
Akademický článek
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Autor:
Freeman, D, Waite, F, Startup, H, Myers, E, Lister, R, McInerney, J, Harvey, A, Geddes, J, Zaiwalla, Z, Luengo-Fernandez, R, Foster, R, Clifton, L, Yu, L
Publikováno v:
The Lancet. Psychiatry
Summary Background Sleep disturbance occurs in most patients with delusions or hallucinations and should be treated as a clinical problem in its own right. However, cognitive behavioural therapy (CBT)—the best evidence-based treatment for insomnia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92781ee713d1c1bbb18ac4a36bf72ddf
https://ora.ox.ac.uk/objects/uuid:7d004e94-ad64-4b82-bb65-67b683a7fffb
https://ora.ox.ac.uk/objects/uuid:7d004e94-ad64-4b82-bb65-67b683a7fffb
Autor:
Rolinski, M, Griffanti, L, Piccini, P, Roussakis, A, Szewczyk-Krolikowski1, K, Menke, R, Quinnell, T, Zaiwalla, Z, Klein, J, Mackay, C, Hu, M
Publikováno v:
Rolinski, M, Griffanti, L, Piccini, P, Roussakis, A A, Szewczyk-Krolikowski, K, Menke, R A, Quinnell, T, Zaiwalla, Z, Klein, J C, Mackay, C E & Hu, M T M 2016, ' Basal ganglia dysfunction in idiopathic REM sleep behaviour disorder parallels that in early Parkinson's disease ', Brain, vol. 139, no. 8, pp. 2224–2234 . https://doi.org/10.1093/brain/aww124
Resting state functional magnetic resonance imaging dysfunction within the basal ganglia network is a feature of early Parkinson's disease and may be a diagnostic biomarker of basal ganglia dysfunction. Currently, it is unclear whether these changes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8f52bbfab55c588a2dfbe3459037cffa
http://hdl.handle.net/10044/1/30929
http://hdl.handle.net/10044/1/30929
Autor:
Rolinski, M, Zokaei, N, Baig, F, Giehl, K, Quinnell, T, Zaiwalla, Z, Mackay, C, Husain, M, Hu, M
Publikováno v:
Rolinski, M, Zokaei, N, Baig, F, Giehl, K, Quinnell, T, Zaiwalla, Z, Mackay, C E, Husain, M & Hu, M T M 2016, ' Visual short-term memory deficits in REM sleep behaviour disorder mirror those in Parkinson's disease ', Brain, vol. 139, no. Pt 1, pp. 47-53 . https://doi.org/10.1093/brain/awv334
Individuals with REM sleep behaviour disorder are at significantly higher risk of developing Parkinson's disease. Here we examined visual short-term memory deficits--long associated with Parkinson's disease--in patients with REM sleep behaviour disor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6183afb2bd3fb6706b675e4caeec822a
https://hdl.handle.net/1983/f2b77b2a-a4d2-420d-99df-ac661b859e7b
https://hdl.handle.net/1983/f2b77b2a-a4d2-420d-99df-ac661b859e7b
Autor:
Martin, H, Kim, G, Pagnamenta, A, Murakami, Y, Carvill, G, Meyer, E, Copley, R, Rimmer, A, Barcia, G, Fleming, MR, Kronengold, J, Brown, MR, Hudspith, K, Broxholme, J, Kanapin, A, Cazier, J, Kinoshita, T, Nabbout, R, Bentley, D, McVean, G, Heavin, S, Zaiwalla, Z, McShane, T, Mefford, H, Shears, D, Stewart, H, Kurian, M, Scheffer, I, Blair, E, Donnelly, P, Kaczmarek, L, Taylor, J
Publikováno v:
Human Molecular Genetics
In severe early-onset epilepsy, precise clinical and molecular genetic diagnosis is complex, as many metabolic and electro-physiological processes have been implicated in disease causation. The clinical phenotypes share many features such as complex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a7066117c7ad78634dae68bbd2cd58ae
http://ora.ox.ac.uk/objects/uuid:0261d765-bc63-4796-bf4b-ab1e096a3828
http://ora.ox.ac.uk/objects/uuid:0261d765-bc63-4796-bf4b-ab1e096a3828