| Cognitive behavioural therapy for adults with dissociative seizures (CODES): a pragmatic, multicentre, randomised controlled trial LH Goldstein, EJ Robinson, JDC Mellers, J Stone, A Carson, M Reuber, ... The Lancet Psychiatry 7 (6), 491-505, 2020 | 218 | 2020 |
| Loss of nuclear TDP‐43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones JR Highley, J Kirby, JA Jansweijer, PS Webb, CA Hewamadduma, ... Neuropathology and applied neurobiology 40 (6), 670-685, 2014 | 192 | 2014 |
| Clinical features of hereditary spastic paraplegia due to spastin mutation CJ McDermott, CE Burness, J Kirby, LE Cox, DG Rao, C Hewamadduma, ... Neurology 67 (1), 45-51, 2006 | 159 | 2006 |
| Chronic idiopathic axonal polyneuropathy: a systematic review P Zis, PG Sarrigiannis, DG Rao, C Hewamadduma, M Hadjivassiliou Journal of neurology 263, 1903-1910, 2016 | 88 | 2016 |
| Value of systematic genetic screening of patients with amyotrophic lateral sclerosis SR Shepheard, MD Parker, J Cooper-Knock, NS Verber, L Tuddenham, ... Journal of Neurology, Neurosurgery & Psychiatry 92 (5), 510-518, 2021 | 82 | 2021 |
| Safety and efficacy of zilucoplan in patients with generalised myasthenia gravis (RAISE): a randomised, double-blind, placebo-controlled, phase 3 study JF Howard, S Bresch, A Genge, C Hewamadduma, J Hinton, Y Hussain, ... The Lancet Neurology 22 (5), 395-406, 2023 | 63 | 2023 |
| Characteristics of 698 patients with dissociative seizures: a UK multicenter study LH Goldstein, EJ Robinson, M Reuber, T Chalder, H Callaghan, ... Epilepsia 60 (11), 2182-2193, 2019 | 63 | 2019 |
| New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP) C Hewamadduma, C McDermott, J Kirby, A Grierson, M Panayi, A Dalton, ... Neurogenetics 10, 105-110, 2009 | 59 | 2009 |
| Tardbpl splicing rescues motor neuron and axonal development in a mutant tardbp zebrafish CAA Hewamadduma, AJ Grierson, TP Ma, L Pan, CB Moens, PW Ingham, ... Human molecular genetics 22 (12), 2376-2386, 2013 | 52 | 2013 |
| Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations CA Hewamadduma, N Hoggard, R O'Malley, MK Robinson, ... Neurology: Genetics 4 (6), e279, 2018 | 48 | 2018 |
| HSP60 IS A RARE CAUSE OF HEREDITARY SPASTIC PARAPARESIS, BUT MAY ACT AS A GENETIC MODIFIER CAA Hewamadduma, J Kirby, C Kershaw, J Martindale, A Dalton, ... Neurology 70 (19), 1717-1718, 2008 | 26 | 2008 |
| Chronic idiopathic axonal polyneuropathy: prevalence of pain and impact on quality of life P Zis, PG Sarrigiannis, DG Rao, C Hewamadduma, M Hadjivassiliou Brain and Behavior 9 (1), e01171, 2019 | 24 | 2019 |
| Adult North Star Network (ANSN): consensus guideline for the standard of care of adults with duchenne muscular dystrophy R Quinlivan, B Messer, P Murphy, R Astin, R Mukherjee, J Khan, ... Journal of Neuromuscular Diseases 8 (6), 899-926, 2021 | 23 | 2021 |
| Genotype–phenotype correlations in valosin-containing protein disease: a retrospective muticentre study M Schiava, C Ikenaga, RN Villar-Quiles, M Caballero-Ávila, A Topf, ... Journal of Neurology, Neurosurgery & Psychiatry 93 (10), 1099-1111, 2022 | 22 | 2022 |
| Rapid identification of human muscle disease with fibre optic Raman spectroscopy JJP Alix, M Plesia, GR Lloyd, AP Dudgeon, CA Kendall, ... Analyst 147 (11), 2533-2540, 2022 | 13 | 2022 |
| MUTATIONS IN VAPB ARE NOT ASSOCIATED WITH SPORADIC ALS J Kirby, CAA Hewamadduma, JA Hartley, HC Nixon, H Evans, ... Neurology 68 (22), 1951-1953, 2007 | 11 | 2007 |
| Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations. Neurol Genet 4 (6): e279 CA Hewamadduma, N Hoggard, R O’Malley, MK Robinson, ... | 10 | 2018 |
| Loss of nuclear TDP-43 in ALS causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurons JR Highley, J Kirby, JA Jansweijer, PS Webb, CA Hewamadduma, ... Neuropathol. Appl. Neurobiol 40, 670-685, 2014 | 9 | 2014 |
| Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy J Park, A Tucci, V Cipriani, G Demidov, C Rocca, J Senderek, M Butryn, ... Genetics in Medicine 24 (10), 2079-2090, 2022 | 7 | 2022 |
| POG09 CADASIL in a mother and son due to a novel mutation of the NOTCH-3 gene C Hewamadduma, KA Harkness, DK Chadha, A Dalton, CJ McDermott Journal of Neurology, Neurosurgery & Psychiatry 81 (11), e50-e50, 2010 | 2 | 2010 |
