Articles with public access mandates - Roger WhittakerLearn more
Not available anywhere: 2
Functional magnetic resonance imaging of human motor unit fasciculation in amyotrophic lateral sclerosis
RG Whittaker, P Porcari, L Braz, TL Williams, IS Schofield, AM Blamire
Annals of neurology 85 (3), 455-459, 2019
Mandates: UK Medical Research Council
W: Ti Intraneural Flexible Electrode for Acute Peripheral Nerve Stimulation Studies
C Silveira, E Brunton, E Escobedo-Cousin, G Gupta, R Whittaker, ...
2020 27th IEEE International Conference on Electronics, Circuits and Systems …, 2020
Mandates: UK Engineering and Physical Sciences Research Council
Available somewhere: 46
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, PG Griffiths, GS Gorman, CM Lourenco, AF Wright, ...
Brain 133 (3), 771-786, 2010
Mandates: German Research Foundation
Genetic heterogeneity of motor neuropathies
B Bansagi, H Griffin, RG Whittaker, T Antoniadi, T Evangelista, J Miller, ...
Neurology 88 (13), 1226-1234, 2017
Mandates: US National Institutes of Health, UK Medical Research Council, National …
Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy
DN Herrmann, R Horvath, JE Sowden, M Gonzales, A Sanchez-Mejias, ...
The American Journal of Human Genetics 95 (3), 332-339, 2014
Mandates: US National Institutes of Health, UK Engineering and Physical Sciences …
Urine heteroplasmy is the best predictor of clinical outcome in the m. 3243A> G mtDNA mutation
RG Whittaker, JK Blackwood, CL Alston, EL Blakely, JL Elson, ...
Neurology 72 (6), 568, 2009
Mandates: German Research Foundation
A nonsynaptic mechanism underlying interictal discharges in human epileptic neocortex
AK Roopun, JD Simonotto, ML Pierce, A Jenkins, C Nicholson, ...
Proceedings of the National Academy of Sciences 107 (1), 338-343, 2010
Mandates: US National Institutes of Health
A guide to approaching regulatory considerations for lentiviral-mediated gene therapies
M White, R Whittaker, C Gandara, EA Stoll
Human gene therapy methods 28 (4), 163-176, 2017
Mandates: UK Engineering and Physical Sciences Research Council, Wellcome Trust
Epilepsy in adults with mitochondrial disease: a cohort study
RG Whittaker, HE Devine, GS Gorman, AM Schaefer, R Horvath, Y Ng, ...
Annals of neurology 78 (6), 949-957, 2015
Mandates: UK Engineering and Physical Sciences Research Council, UK Medical Research …
Human brain slices for epilepsy research: Pitfalls, solutions and future challenges
RSG Jones, AB da Silva, RG Whittaker, GL Woodhall, MO Cunningham
Journal of neuroscience methods 260, 221-232, 2016
Mandates: UK Medical Research Council, Wellcome Trust
Gap junction networks can generate both ripple‐like and fast ripple‐like oscillations
A Simon, RD Traub, N Vladimirov, A Jenkins, C Nicholson, RG Whittaker, ...
European Journal of Neuroscience 39 (1), 46-60, 2014
Mandates: US National Institutes of Health, UK Medical Research Council, Wellcome Trust
Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndrome
RG Whittaker, DN Herrmann, B Bansagi, BAS Hasan, RM Lofra, ...
Neurology 85 (22), 1964-1971, 2015
Mandates: US National Institutes of Health, UK Engineering and Physical Sciences …
Prevalence of active epilepsy in rural Tanzania: a large community-based survey in an adult population
E Hunter, J Rogathi, S Chigudu, A Jusabani, M Jackson, R McNally, ...
Seizure 21 (9), 691-698, 2012
Mandates: Department of International Development, UK
Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease
NZ Lax, J Grady, A Laude, F Chan, PD Hepplewhite, G Gorman, ...
Neuropathology and applied neurobiology 42 (2), 180-193, 2016
Mandates: UK Medical Research Council, National Institute for Health Research, UK …
Congenital myasthenic syndrome with episodic apnoea: clinical, neurophysiological and genetic features in the long-term follow-up of 19 patients
G McMacken, RG Whittaker, T Evangelista, A Abicht, M Dusl, ...
Journal of Neurology 265, 194-203, 2018
Mandates: UK Medical Research Council, Wellcome Trust
Forecasting stroke-like episodes and outcomes in mitochondrial disease
YS Ng, NZ Lax, AP Blain, D Erskine, MR Baker, T Polvikoski, RH Thomas, ...
Brain 145 (2), 542-554, 2022
Mandates: Alzheimers's UK, UK Biotechnology and Biological Sciences Research Council …
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease
V Boczonadi, MS King, AC Smith, M Olahova, B Bansagi, A Roos, ...
Genetics in Medicine 20 (10), 1224-1235, 2018
Mandates: UK Medical Research Council, National Institute for Health Research, UK …
Non-invasive imaging of single human motor units
MG Birkbeck, L Heskamp, IS Schofield, AM Blamire, RG Whittaker
Clinical Neurophysiology 131 (6), 1399-1406, 2020
Mandates: UK Medical Research Council, National Institute for Health Research, UK
Glissandi: transient fast electrocorticographic oscillations of steadily increasing frequency, explained by temporally increasing gap junction conductance
MO Cunningham, A Roopun, IS Schofield, RG Whittaker, R Duncan, ...
Epilepsia 53 (7), 1205-1214, 2012
Mandates: US National Institutes of Health
Two common psychophysical measures of surround suppression reflect independent neuronal mechanisms
P Yazdani, I Serrano-Pedraza, RG Whittaker, A Trevelyan, JCA Read
Journal of vision 15 (13), 21-21, 2015
Mandates: UK Medical Research Council, Government of Spain
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