Roger Whittaker - Publications

Affiliations: 
Institute of Neuroscience Newcastle University, Newcastle upon Tyne, England, United Kingdom 

48 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Birkbeck MG, Heskamp L, Schofield IS, Blamire AM, Whittaker RG. Non-invasive imaging of single human motor units. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. PMID 32122767 DOI: 10.1016/j.clinph.2020.02.004  0.4
2019 Whittaker RG, Porcari P, Braz L, Williams TL, Schofield IS, Blamire AM. Functional MR imaging of human motor unit fasciculation in Amyotrophic Lateral Sclerosis. Annals of Neurology. PMID 30688362 DOI: 10.1002/ana.25422  0.4
2016 Whittaker RG, Gorman G, Ng Y, Turnbull DM. Reply to 'Prevalence and outcome of mitochondrial epilepsy' Finsterer and Zarrouk-Mahjoub. Annals of Neurology. PMID 27393207 DOI: 10.1002/ana.24722  0.72
2016 Hunter E, Rogathi J, Chigudu S, Jusabani A, Jackson M, Whittaker RG, Gray W, McNally RJ, Aris E, Mushi D, Walker R. The epilepsy treatment gap in rural Tanzania: A community-based study in adults. Seizure. 36: 49-56. PMID 26938970 DOI: 10.1016/j.seizure.2016.02.008  0.72
2015 Jones RS, da Silva AB, Whittaker RG, Woodhall GL, Cunningham MO. Human brain slices for epilepsy research: Pitfalls, solutions and future challenges. Journal of Neuroscience Methods. PMID 26434706 DOI: 10.1016/j.jneumeth.2015.09.021  0.72
2015 Yazdani P, Serrano-Pedraza I, Whittaker RG, Trevelyan A, Read JC. Two common psychophysical measures of surround suppression reflect independent neuronal mechanisms. Journal of Vision. 15: 21. PMID 26401628 DOI: 10.1167/15.13.21  0.56
2015 Whittaker RG, Devine HE, Gorman GS, Schaefer AM, Horvath R, Ng Y, Nesbitt V, Lax NZ, McFarland R, Cunningham MO, Taylor RW, Turnbull DM. Epilepsy in adults with mitochondrial disease: A cohort study. Annals of Neurology. PMID 26381753 DOI: 10.1002/ana.24525  0.72
2015 Whittaker RG. Video telemetry: current concepts and recent advances. Practical Neurology. PMID 26271266 DOI: 10.1136/practneurol-2015-001216  0.72
2015 Lax NZ, Grady J, Laude A, Chan F, Hepplewhite PD, Gorman G, Whittaker RG, Ng Y, Cunningham MO, Turnbull DM. Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease. Neuropathology and Applied Neurobiology. PMID 25786813 DOI: 10.1111/nan.12238  0.72
2014 Herrmann DN, Horvath R, Sowden JE, Gonzalez M, Gonzales M, Sanchez-Mejias A, Guan Z, Whittaker RG, Almodovar JL, Lane M, Bansagi B, Pyle A, Boczonadi V, Lochmüller H, Griffin H, et al. Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy. American Journal of Human Genetics. 95: 332-9. PMID 25192047 DOI: 10.1016/j.ajhg.2014.08.007  0.72
2014 Simon A, Traub RD, Vladimirov N, Jenkins A, Nicholson C, Whittaker RG, Schofield I, Clowry GJ, Cunningham MO, Whittington MA. Gap junction networks can generate both ripple-like and fast ripple-like oscillations. The European Journal of Neuroscience. 39: 46-60. PMID 24118191 DOI: 10.1111/ejn.12386  0.72
2013 Jaiser SR, Baker MR, Whittaker RG, Birchall D, Chinnery PF. Clinical reasoning: a 39-year-old man with abdominal cramps. Neurology. 81: e5-9. PMID 23836948 DOI: 10.1212/WNL.0b013e31829a335e  0.72
2013 Whittaker RG, Hall E, Mansoor MK, Taylor RW, Turnbull DM. Incidence of carpal tunnel syndrome in adult patients with mitochondrial disease. Journal of the Peripheral Nervous System : Jpns. 18: 59-61. PMID 23521646 DOI: 10.1111/jns5.12009  0.72
2013 Elson JL, Cadogan M, Apabhai S, Whittaker RG, Phillips A, Trennell MI, Horvath R, Taylor RW, McFarland R, McColl E, Turnbull DM, Gorman GS. Initial development and validation of a mitochondrial disease quality of life scale. Neuromuscular Disorders : Nmd. 23: 324-9. PMID 23433484 DOI: 10.1016/j.nmd.2012.12.012  0.72
2013 Whittaker RG. All diagnoses are clinical, but some are more clinical than others. Practical Neurology. 13: 1. PMID 23315470 DOI: 10.1136/practneurol-2012-000472  0.72
2013 Kosac A, Gavillet E, Whittaker RG. Neurophysiological testing in congenital myasthenic syndromes: A systematic review of published normal data Muscle and Nerve. 48: 711-715. DOI: 10.1002/mus.23929  0.72
2012 Whittaker RG. Why the curious incident of the dog in the night was 'contributory'. Practical Neurology. 12: 397. PMID 23144310 DOI: 10.1136/practneurol-2012-000415  0.72
2012 Basu AP, Bellis P, Whittaker RG, McKean MC, Devlin AM. Teaching NeuroImages: alternating ptosis and Marcus Gunn jaw-winking phenomenon with PHOX2B mutation. Neurology. 79: e153. PMID 23091080 DOI: 10.1212/WNL.0b013e3182703fe3  0.72
2012 Hunter E, Rogathi J, Chigudu S, Jusabani A, Jackson M, McNally R, Gray W, Whittaker RG, Iqbal A, Birchall D, Aris E, Walker R. Prevalence of active epilepsy in rural Tanzania: a large community-based survey in an adult population. Seizure. 21: 691-8. PMID 22883631 DOI: 10.1016/j.seizure.2012.07.009  0.72
2012 Brown SM, Williams TL, Whittaker RG. A cautionary tale: threatened compartment syndrome following electromyography in an anticoagulated patient. Muscle & Nerve. 46: 144-5; author reply . PMID 22693007 DOI: 10.1002/mus.23376  0.72
2012 Cunningham MO, Roopun A, Schofield IS, Whittaker RG, Duncan R, Russell A, Jenkins A, Nicholson C, Whittington MA, Traub RD. Glissandi: transient fast electrocorticographic oscillations of steadily increasing frequency, explained by temporally increasing gap junction conductance. Epilepsia. 53: 1205-14. PMID 22686654 DOI: 10.1111/j.1528-1167.2012.03530.x  0.72
2012 Whittaker RG. The fundamentals of electromyography. Practical Neurology. 12: 187-94. PMID 22661353 DOI: 10.1136/practneurol-2011-000198  0.72
2012 Whittaker RG. SNAPs, CMAPs and F-waves: nerve conduction studies for the uninitiated. Practical Neurology. 12: 108-15. PMID 22450459 DOI: 10.1136/practneurol-2011-000126  0.72
2012 Burton KJ, Rogathe J, Whittaker R, Mankad K, Hunter E, Burton MJ, Todd J, Neville BG, Walker R, Newton CR. Epilepsy in Tanzanian children: association with perinatal events and other risk factors. Epilepsia. 53: 752-60. PMID 22308971 DOI: 10.1111/j.1528-1167.2011.03395.x  0.72
2012 Read JL, Whittaker RG, Miller N, Clark S, Taylor R, McFarland R, Turnbull D. Prevalence and severity of voice and swallowing difficulties in mitochondrial disease. International Journal of Language & Communication Disorders / Royal College of Speech & Language Therapists. 47: 106-11. PMID 22268906 DOI: 10.1111/j.1460-6984.2011.00072.x  0.72
2012 Lax NZ, Whittaker RG, Hepplewhite PD, Reeve AK, Blakely EL, Jaros E, Ince PG, Taylor RW, Fawcett PR, Turnbull DM. Sensory neuronopathy in patients harbouring recessive polymerase γ mutations. Brain : a Journal of Neurology. 135: 62-71. PMID 22189570 DOI: 10.1093/brain/awr326  0.72
2012 Burton K, Rogathe J, Whittaker RG, Mankad K, Hunter E, Burton MJ, Todd J, Neville BG, Walker R, Newton CR. Co-morbidity of epilepsy in Tanzanian children: a community-based case-control study. Seizure. 21: 169-74. PMID 22130004 DOI: 10.1016/j.seizure.2011.10.011  0.72
2011 Whittaker RG. Testing the neuromuscular junction: what neurophysiology can offer the neurologist. Practical Neurology. 11: 303-7. PMID 21921007 DOI: 10.1136/practneurol-2011-000029  0.72
2011 Baker MR, Fisher KM, Whittaker RG, Griffiths PG, Yu-Wai-Man P, Chinnery PF. Subclinical multisystem neurologic disease in "pure" OPA1 autosomal dominant optic atrophy. Neurology. 77: 1309-12. PMID 21917770 DOI: 10.1212/WNL.0b013e318230a15a  0.72
2011 Whittaker RG, Turnbull DM, Whittington MA, Cunningham MO. Impaired mitochondrial function abolishes gamma oscillations in the hippocampus through an effect on fast-spiking interneurons. Brain : a Journal of Neurology. 134: e180; author reply e. PMID 21378098 DOI: 10.1093/brain/awr018  0.72
2011 Romaniuk L, Turnbull DM, Whittaker RG. Hyperventilation during the EEG is safe in mitochondrial disease. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 122: 1270-1. PMID 21111674 DOI: 10.1016/j.clinph.2010.10.039  0.72
2011 Nesbitt V, Whittaker RG, Turnbull DM, McFarland R, Taylor RW. MtDNA disease for the neurologist Future Neurology. 6: 63-80. DOI: 10.2217/fnl.10.70  0.72
2010 Elson JL, Apabhai S, Gorman G, Whittaker RG, Krishnan KJ. Older mothers are not at risk of having grandchildren with sporadic mtDNA deletions. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 12: 313-4. PMID 20474085 DOI: 10.1097/GIM.0b013e3181da76e3  0.72
2010 Blackwood JK, Whittaker RG, Blakely EL, Alston CL, Turnbull DM, Taylor RW. The investigation and diagnosis of pathogenic mitochondrial DNA mutations in human urothelial cells. Biochemical and Biophysical Research Communications. 393: 740-5. PMID 20171163 DOI: 10.1016/j.bbrc.2010.02.072  0.72
2010 Kisler JE, Whittaker RG, McFarland R. Mitochondrial diseases in childhood: a clinical approach to investigation and management. Developmental Medicine and Child Neurology. 52: 422-33. PMID 20163433 DOI: 10.1111/j.1469-8749.2009.03605.x  0.72
2010 Yu-Wai-Man P, Griffiths PG, Gorman GS, Lourenco CM, Wright AF, Auer-Grumbach M, Toscano A, Musumeci O, Valentino ML, Caporali L, Lamperti C, Tallaksen CM, Duffey P, Miller J, Whittaker RG, et al. Multi-system neurological disease is common in patients with OPA1 mutations. Brain : a Journal of Neurology. 133: 771-86. PMID 20157015 DOI: 10.1093/brain/awq007  0.72
2010 Roopun AK, Simonotto JD, Pierce ML, Jenkins A, Nicholson C, Schofield IS, Whittaker RG, Kaiser M, Whittington MA, Traub RD, Cunningham MO. A nonsynaptic mechanism underlying interictal discharges in human epileptic neocortex. Proceedings of the National Academy of Sciences of the United States of America. 107: 338-43. PMID 19966298 DOI: 10.1073/pnas.0912652107  0.72
2009 Al-Dosary M, Whittaker RG, Haughton J, McFarland R, Goodship J, Turnbull DM, Taylor RW. Neuromuscular disease presentation with three genetic defects involving two genomes. Neuromuscular Disorders : Nmd. 19: 841-4. PMID 19853445 DOI: 10.1016/j.nmd.2009.10.001  0.72
2009 Whittaker RG, Blackwood JK, Alston CL, Blakely EL, Elson JL, McFarland R, Chinnery PF, Turnbull DM, Taylor RW. Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation. Neurology. 72: 568-9. PMID 19204268 DOI: 10.1212/01.wnl.0000342121.91336.4d  0.72
2009 Whittaker RG, Turnbull DM. A diagnostic tattoo. Clinical Genetics. 75: 37-8. PMID 19128396 DOI: 10.1111/j.1399-0004.2008.01103.x  0.72
2009 Roopun AK, Traub RD, Baldeweg T, Cunningham MO, Whittaker RG, Trevelyan A, Duncan R, Russell AJ, Whittington MA. Detecting seizure origin using basic, multiscale population dynamic measures: preliminary findings. Epilepsy & Behavior : E&B. 14: 39-46. PMID 18834957 DOI: 10.1016/j.yebeh.2008.09.008  0.72
2008 Moriarty KT, McFarland R, Whittaker R, Burch J, Turnbull HE, Taylor RW, Turnbull DM. Pre-eclampsia and magnesium toxicity with therapeutic plasma level in a woman with m.3243A>G melas mutation. Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology. 28: 349. PMID 18569490 DOI: 10.1080/01443610802048545  0.72
2008 Schaefer AM, McFarland R, Blakely EL, He L, Whittaker RG, Taylor RW, Chinnery PF, Turnbull DM. Prevalence of mitochondrial DNA disease in adults. Annals of Neurology. 63: 35-9. PMID 17886296 DOI: 10.1002/ana.21217  0.72
2008 Schaefer AM, Whittaker R, McFarland R, Chinnery PF, Taylor RW, Turnbull DM. Reply Annals of Neurology. 64: 471-472. DOI: 10.1002/ANA.21967  0.72
2007 Whittaker RG, Schaefer AM, McFarland R, Taylor RW, Walker M, Turnbull DM. Prevalence and progression of diabetes in mitochondrial disease. Diabetologia. 50: 2085-9. PMID 17653689 DOI: 10.1007/s00125-007-0779-9  0.72
2007 Whittaker RG, Schaefer AM, McFarland R, Taylor RW, Walker M, Turnbull DM. Diabetes and deafness: is it sufficient to screen for the mitochondrial 3243A>G mutation alone? Diabetes Care. 30: 2238-9. PMID 17540956 DOI: 10.2337/dc07-0466  0.72
2007 Whittaker R, Scott A, Gardner M. The prevalence of prolonged cerebral seizures at the first treatment in a course of electroconvulsive therapy. The Journal of Ect. 23: 11-3. PMID 17435565 DOI: 10.1097/01.yct.0000263253.14044.3a  0.72
2007 Whittaker RG, Schaefer AM, Taylor RW, Turnbull DM. Differential diagnosis in ptosis and ophthalmoplegia: mitochondrial disease or myasthenia? Journal of Neurology. 254: 1138-9. PMID 17361341 DOI: 10.1007/s00415-006-0484-5  0.72
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