Roger Whittaker
Roger Whittaker
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Prevalence of mitochondrial DNA disease in adults
AM Schaefer, R McFarland, EL Blakely, L He, RG Whittaker, RW Taylor, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
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
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), 568-569, 2009
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
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
The extended deltoid-splitting approach to the proximal humerus
CM Robinson, L Khan, A Akhtar, R Whittaker
Journal of orthopaedic trauma 21 (9), 657-662, 2007
Mitochondrial diseases in childhood: a clinical approach to investigation and management
JE Kisler, RG Whittaker, R McFarland
Developmental Medicine & Child Neurology 52 (5), 422-433, 2010
Genetic heterogeneity of motor neuropathies
B Bansagi, H Griffin, RG Whittaker, T Antoniadi, T Evangelista, J Miller, ...
Neurology 88 (13), 1226-1234, 2017
Sensory neuronopathy in patients harbouring recessive polymerase γ mutations
NZ Lax, RG Whittaker, PD Hepplewhite, AK Reeve, EL Blakely, E Jaros, ...
Brain 135 (1), 62-71, 2012
Prevalence and progression of diabetes in mitochondrial disease
RG Whittaker, AM Schaefer, R McFarland, RW Taylor, M Walker, ...
Diabetologia 50 (10), 2085-2089, 2007
Epilepsy in Tanzanian children: association with perinatal events and other risk factors
KJ Burton, J Rogathe, R Whittaker, K Mankad, E Hunter, MJ Burton, ...
Epilepsia 53 (4), 752-760, 2012
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
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
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
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
Assessment of axillary nerve function and functional outcome after fixation of complex proximal humeral fractures using the extended deltoid-splitting approach
LAK Khan, CM Robinson, E Will, R Whittaker
Injury 40 (2), 181-185, 2009
Myotonic dystrophy: practical issues relating to assessment of strength
RG Whittaker, E Ferenczi, D Hilton-Jones
Journal of Neurology, Neurosurgery & Psychiatry 77 (11), 1282-1283, 2006
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
Impaired mitochondrial function abolishes gamma oscillations in the hippocampus through an effect on fast-spiking interneurons
RG Whittaker, DM Turnbull, MA Whittington, MO Cunningham
Brain 134 (7), e180-e180, 2011
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
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