Items where authors include "McDermott, C.J."

Article

Boddy, S.L., Simpson, R.M. orcid.org/0000-0003-1677-5938, Walters, S.J. et al. (38 more authors) (2025) Further development of a patient-reported outcome measure to assess the impact of oral secretion problems in people living with MND. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. ISSN 2167-8421

Murray, D. orcid.org/0000-0002-4314-4480, Rooney, J. orcid.org/0000-0001-6346-0731, Meldrum, D. orcid.org/0000-0002-7732-3591 et al. (18 more authors) (2025) Respiratory measurements, respiratory symptoms, and quality of life in ALS: results from the REVEALS study. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. ISSN 2167-8421

Howard, J. orcid.org/0000-0001-7182-593X, Bekker, H.L. orcid.org/0000-0003-1978-5795, McDermott, C.J. orcid.org/0000-0002-1269-9053 et al. (1 more author) (2025) Exploring the needs and preferences of people with amyotrophic lateral sclerosis (ALS) when making genomic testing decisions: an interview study. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. ISSN 2167-8421

Boddy, S.L., Simpson, R.M. orcid.org/0000-0003-1677-5938, Walters, S.J. orcid.org/0000-0001-9000-8126 et al. (3 more authors) (2025) Estimating the minimum important difference in the ALSFRS-R-instrument in people living with MND. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. ISSN 2167-8421

Qiang, Z., Barnett, L., Bingham, G. et al. (7 more authors) (2024) The diagnostic journey of patients being investigated for myopathy in a tertiary centre in England. Journal of Neurology, 272 (1). 35. ISSN 0340-5354

Roscoe, S.A. orcid.org/0000-0001-5292-625X, Allen, S.P. orcid.org/0000-0003-4418-7375, McDermott, C.J. orcid.org/0000-0002-1269-9053 et al. (1 more author) (2024) Mapping the evidence for measuring energy expenditure and indicating hypermetabolism in motor neuron disease: a scoping review. Nutrition Reviews. nuae118. ISSN 0029-6643

McDool, E. orcid.org/0000-0002-3530-7921, Carlton, J. orcid.org/0000-0002-9373-7663, Powell, P.A. orcid.org/0000-0003-1169-3431 et al. (7 more authors) (2024) Measuring health-related quality of life in amyotrophic lateral sclerosis. Neurology, 103 (2). e209549. ISSN 0028-3878

Howard, J. orcid.org/0000-0001-7182-593X, Bekker, H.L., McDermott, C.J. orcid.org/0000-0002-1269-9053 et al. (1 more author) (2024) Survey of service needs to embed genome sequencing for motor neuron disease in neurology in the English National Health Service. Journal of Medical Genetics, 61 (7). pp. 661-665. ISSN 0022-2593

Rooney, J. orcid.org/0000-0001-6346-0731, Murray, D. orcid.org/0000-0002-4314-4480, Meldrum, D. orcid.org/0000-0002-7732-3591 et al. (18 more authors) (2024) REVEALS—a longitudinal cohort study of multifaceted respiratory assessment in ALS. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 25 (7-8). pp. 661-671. ISSN 2167-8421

Gould, R.L., McDermott, C.J., Thompson, B.J. orcid.org/0000-0002-5516-8797 et al. (29 more authors) (2024) Acceptance and Commitment Therapy plus usual care for improving quality of life in people with motor neuron disease (COMMEND): a multicentre, parallel, randomised controlled trial in the UK. The Lancet, 403 (10442). pp. 2381-2394. ISSN 0140-6736

Van Damme, P. orcid.org/0000-0002-4010-2357, Al‐Chalabi, A. orcid.org/0000-0002-4924-7712, Andersen, P.M. et al. (17 more authors) (2024) European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO-NMD). European Journal of Neurology, 31 (6). e16264. ISSN 1351-5101

Alix, J.J.P. orcid.org/0000-0001-8391-9749, Plesia, M., Dudgeon, A.P. orcid.org/0000-0002-4536-1147 et al. (9 more authors) (2024) Conformational fingerprinting with Raman spectroscopy reveals protein structure as a translational biomarker of muscle pathology. The Analyst, 149 (9). pp. 2738-2746. ISSN 0003-2654

White, S., O’Cathain, A., Halliday, V. orcid.org/0000-0003-2458-5253 et al. (2 more authors) (2024) Supporting people with Motor Neuron Disease (MND) to make decisions about gastrostomy feeding tube placement: a survey of UK healthcare professionals’ practice and beliefs. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 25 (3-4). pp. 290-298. ISSN 2167-8421

Howard, J., Bekker, H.L orcid.org/0000-0003-1978-5795, McDermott, C.J. et al. (1 more author) (2024) Survey of service needs to embed genome sequencing for motor neuron disease in neurology in the English National Health Service. Journal of Medical Genetics. ISSN 0022-2593

Rawlinson, C., Gould, R.L., McDermott, C.J. orcid.org/0000-0002-1269-9053 et al. (27 more authors) (2024) Experiences of acceptance and commitment therapy for people living with motor neuron disease (MND): a qualitative study from the perspective of people living with MND and therapists. The Cognitive Behaviour Therapist, 17. e36. ISSN 1754-470X

Lombardo, F.L. orcid.org/0000-0001-6183-0735, Spila Alegiani, S., Mayer, F. et al. (93 more authors) (2023) A randomized double-blind clinical trial on safety and efficacy of tauroursodeoxycholic acid (TUDCA) as add-on treatment in patients affected by amyotrophic lateral sclerosis (ALS): the statistical analysis plan of TUDCA-ALS trial. Trials, 24 (1). 792. ISSN 1468-6708

Richardson, P.J. orcid.org/0000-0001-7813-041X, Smith, D.P., de Giorgio, A. et al. (6 more authors) (2023) Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis. Translational Neurodegeneration, 12 (1). 47. ISSN 2047-9158

Gwathmey, K.G. orcid.org/0000-0002-7589-8826, Corcia, P., McDermott, C.J. orcid.org/0000-0002-1269-9053 et al. (4 more authors) (2023) Diagnostic delay in amyotrophic lateral sclerosis. European Journal of Neurology, 30 (9). pp. 2595-2601. ISSN 1351-5101

White, S. orcid.org/0000-0002-6865-9624, O'Cathain, A. orcid.org/0000-0003-4033-506X, Halliday, V. et al. (2 more authors) (2023) Factors influencing decisions people with motor neuron disease make about gastrostomy placement and ventilation: a qualitative evidence synthesis. Health Expectations, 26 (4). pp. 1418-1435. ISSN 1369-6513

Gould, R.L. orcid.org/0000-0001-9283-1626, Rawlinson, C., Thompson, B. et al. (43 more authors) (2023) Acceptance and commitment therapy for people living with motor neuron disease: an uncontrolled feasibility study. Pilot and Feasibility Studies, 9. 116. ISSN 2055-5784

Musson, L.S. orcid.org/0000-0002-1246-2734, Baxter, S.K., Norman, P. orcid.org/0000-0002-5892-0470 et al. (7 more authors) (2023) Delivery of non-invasive ventilation to people living with motor neuron disease in the UK. ERJ Open Research, 9 (2). 00388-2022. ISSN 2312-0541

Alix, J.J.P. orcid.org/0000-0001-8391-9749, Plesia, M., Schooling, C.N. et al. (9 more authors) (2023) Non‐negative matrix factorisation of Raman spectra finds common patterns relating to neuromuscular disease across differing equipment configurations, preclinical models and human tissue. Journal of Raman Spectroscopy, 54 (3). pp. 258-268. ISSN 0377-0486

Gould, R.L., Thompson, B.J. orcid.org/0000-0002-5516-8797, Rawlinson, C. et al. (15 more authors) (2022) A randomised controlled trial of acceptance and commitment therapy plus usual care compared to usual care alone for improving psychological health in people with motor neuron disease (COMMEND): study protocol. BMC Neurology, 22 (1). 431. ISSN 1471-2377

Albanese, A., Ludolph, A.C., McDermott, C.J. orcid.org/0000-0002-1269-9053 et al. (7 more authors) (2022) Tauroursodeoxycholic acid in patients with amyotrophic lateral sclerosis: the TUDCA-ALS trial protocol. Frontiers in Neurology, 13. 1009113. ISSN 1664-2295

Miller, T.M., Cudkowicz, M.E., Genge, A. et al. (23 more authors) (2022) Trial of antisense oligonucleotide tofersen for SOD1 ALS. New England Journal of Medicine, 387 (12). pp. 1099-1110. ISSN 0028-4793

Burchardt, J.M., Mei, X.W., Ranger, T. et al. (4 more authors) (2022) Analysis of incidence of motor neuron disease in England 1998–2019 : use of three linked datasets. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 23 (5-6). pp. 363-371. ISSN 2167-8421

Schooling, C.N., Healey, T.J., McDonough, H.E. et al. (5 more authors) (2022) Tensor electrical impedance myography identifies bulbardisease progression in amyotrophic lateral sclerosis. Clinical Neurophysiology, 139. pp. 69-75. ISSN 1388-2457

Mei, X.W., Burchardt, J., Ranger, T.A. et al. (4 more authors) (2022) Identifying key signs of motor neurone disease in primary care : a nested case–control study using the QResearch database. BMJ Open, 12 (6). e058383.

Musson, L.S. orcid.org/0000-0002-1246-2734, Collins, A., Opie-Martin, S. orcid.org/0000-0003-0951-8589 et al. (8 more authors) (2022) Impact of the covid-19 pandemic on amyotrophic lateral sclerosis care in the UK. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 2022. pp. 1-9. ISSN 2167-8421

Alix, J.J.P. orcid.org/0000-0001-8391-9749, Plesia, M., Lloyd, G.R. et al. (7 more authors) (2022) The application of Raman spectroscopy to the diagnosis of mitochondrial muscle disease : a preliminary comparison between fibre optic probe and microscope formats. Journal of Raman Spectroscopy, 53 (2). pp. 172-181. ISSN 0377-0486

Chan, Y., Alix, J.J.P. orcid.org/0000-0001-8391-9749, Neuwirth, C. et al. (9 more authors) (2022) Reinnervation as measured by the motor unit size index is associated with preservation of muscle strength in amyotrophic lateral sclerosis but not all muscles reinnervate. Muscle & Nerve, 65 (2). pp. 203-210. ISSN 0148-639X

Thompson, A.G., Gray, E., Verber, N. et al. (20 more authors) (2022) Multicentre appraisal of amyotrophic lateral sclerosis biofluid biomarkers shows primacy of blood neurofilament light chain. Brain Communications, 4 (1). fcac029. ISSN 2632-1297

Schooling, C.N. orcid.org/0000-0001-7892-9715, Healey, T.J., McDonough, H.E. et al. (5 more authors) (2021) Tensor electrical impedance myography identifies clinically relevant features in amyotrophic lateral sclerosis. Physiological Measurement, 42 (10). 105004. ISSN 0967-3334

van Eijk, R.P.A., Nikolakopoulos, S., Roes, K.C.B. et al. (14 more authors) (2021) Innovating clinical trials for amyotrophic lateral sclerosis : challenging the established order. Neurology, 97 (11). pp. 528-536. ISSN 0028-3878

van Eijk, R.P.A., Beelen, A., Kruitwagen, E.T. et al. (16 more authors) (2021) A road map for remote digital health technology for motor neuron disease. Journal of Medical Internet Research, 23 (9). e28766. ISSN 1438-8871

Conroy, É., Kennedy, P., Heverin, M. et al. (8 more authors) (2021) Informal caregivers in amyotrophic lateral sclerosis : a multi-centre, exploratory study of burden and difficulties. Brain Sciences, 11 (8). 1094.

Shepheard, S.R., Parker, M.D. orcid.org/0000-0003-2999-3870, Cooper-Knock, J. orcid.org/0000-0002-0873-8689 et al. (15 more authors) (2021) Value of systematic genetic screening of patients with amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery & Psychiatry, 92 (5). pp. 510-518. ISSN 0022-3050

van Eijk, R.P.A., de Jongh, A.D., Nikolakopoulos, S. et al. (4 more authors) (2021) An old friend who has overstayed their welcome : the ALSFRS-R total score as primary endpoint for ALS clinical trials. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 22 (3-4). pp. 300-307. ISSN 2167-8421

Boddy, S.L., Giovannelli, I., Sassani, M. orcid.org/0000-0002-0384-7296 et al. (7 more authors) (2021) The gut microbiome: a key player in the complexity of amyotrophic lateral sclerosis (ALS). BMC Medicine, 19 (1). 13. ISSN 1741-7015

Schooling, C.N., Jamie Healey, T., McDonough, H.E. et al. (5 more authors) (2020) Modelling and analysis of electrical impedance myography of the lateral tongue. Physiological Measurement, 41 (12). 125008. ISSN 0967-3334

Aggarwal, A., Stavroulakis, T. orcid.org/0000-0002-3535-7822 and McDermott, C.J. orcid.org/0000-0002-1269-9053 (2020) The impact of gastrostomy feeding on the lives of patients: a systematic review. Clinical Nutrition ESPEN, 40. p. 519. ISSN 2405-4577

Sproson, L., Lanfranchi, V. orcid.org/0000-0003-3148-2535, Collins, A. et al. (16 more authors) (2020) Fit for purpose? A cross-sectional study to evaluate the acceptability and usability of HeadUp, a novel neck support collar for neurological neck weakness. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 22 (1-2). pp. 38-45. ISSN 2167-8421

Miller, T., Cudkowicz, M., Shaw, P.J. orcid.org/0000-0002-8925-2567 et al. (28 more authors) (2020) Phase 1–2 Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS. New England Journal of Medicine, 383 (2). pp. 109-119. ISSN 0028-4793

van Eijk, R.P.A., Kliest, T., McDermott, C.J. orcid.org/0000-0002-1269-9053 et al. (12 more authors) (2020) TRICALS: creating a highway toward a cure. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 21 (7-8). pp. 496-501. ISSN 2167-8421

Alix, J.J.P. orcid.org/0000-0001-8391-9749, McDonough, H.E., Sonbas, B. et al. (6 more authors) (2020) Multi-dimensional electrical impedance myography of the tongue as a potential biomarker for amyotrophic lateral sclerosis. Clinical Neurophysiology, 131 (4). pp. 799-808. ISSN 1388-2457

Jenkins, T.M., Alix, J.J.P. orcid.org/0000-0001-8391-9749, Fingret, J. et al. (6 more authors) (2020) Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease. Journal of Neurology, 267 (1). pp. 244-256. ISSN 0340-5354

Maunsell, R., Bloomfield, S., Erridge, C. et al. (12 more authors) (2019) Developing a web-based patient decision aid for gastrostomy in motor neuron disease : a study protocol. BMJ Open, 9 (12). e032364. ISSN 2044-6055

Hobson, E. orcid.org/0000-0002-8497-2338, Baird, W. orcid.org/0000-0002-4253-2721, Bradburn, M. orcid.org/0000-0002-3783-9761 et al. (6 more authors) (2019) Process evaluation and exploration of telehealth in motor neuron disease in a UK specialist centre. BMJ Open, 9. e028526.

Hobson, E.V. orcid.org/0000-0002-8497-2338, Baird, W.O. orcid.org/0000-0002-4253-2721, Bradburn, M. orcid.org/0000-0002-3783-9761 et al. (6 more authors) (2019) Using telehealth in motor neuron disease to increase access to specialist multidisciplinary care : a UK-based pilot and feasibility study. BMJ Open, 9 (10). e028525.

Judge, S. orcid.org/0000-0001-5119-8094, Bloch, S. orcid.org/0000-0002-5355-8134 and McDermott, C.J. orcid.org/0000-0002-1269-9053 (2019) Communication change in ALS: engaging people living with ALS and their partners in future research. Disability and Rehabilitation: Assistive Technology, 14 (7). pp. 675-681. ISSN 1748-3107

Musson, L.S. orcid.org/0000-0002-1246-2734, McDermott, C.J. orcid.org/0000-0002-1269-9053 and Hobson, E.V. orcid.org/0000-0002-8497-2338 (2019) Exploring patient and public involvement in motor neuron disease research. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 20 (7-8). pp. 511-520. ISSN 2167-8421

van den Berg, L.H., Sorenson, E., Gronseth, G. et al. (20 more authors) (2019) Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials. Neurology, 92 (14). e1610-e1623. ISSN 0028-3878

Cooper-Knock, J., Moll, T., Ramesh, T. et al. (26 more authors) (2019) Mutations in the glycosyltransferase domain of GLT8D1 are associated with familial amyotrophic lateral sclerosis. Cell Reports, 26 (9). 2298-2306.e5. ISSN 2211-1247

Hewamadduma, C.A., Hoggard, N. orcid.org/0000-0002-6447-7639, O'Malley, R. et al. (13 more authors) (2018) Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations. Neurology Genetics, 4 (6). e279.

Pancani, S., Tindale, W., Shaw, P.J. et al. (2 more authors) (2018) Efficacy of the Head Up collar in facilitating functional head movements in patients with Amyotrophic Lateral Sclerosis. Clinical Biomechanics, 57. pp. 114-120. ISSN 1879-1271

Westeneng, H.-J., Debray, T.P.A., Visser, A.E. et al. (44 more authors) (2018) Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model. Lancet Neurology, 17 (5). pp. 423-433. ISSN 1474-4422

Cooper-Knock, J. orcid.org/0000-0002-0873-8689, Robins, H., Niedermoser, I. et al. (11 more authors) (2017) Targeted Genetic Screen in Amyotrophic Lateral Sclerosis Reveals Novel Genetic Variants with Synergistic Effect on Clinical Phenotype. Frontiers in Molecular Neuroscience, 10. 370. ISSN 1662-5099

Baxter, S.K. orcid.org/0000-0002-6034-5495 and McDermott, C.J. (2017) Decision-making and referral processes for patients with motor neurone disease: a qualitative study of GP experiences and evaluation of a new decision-support tool. BMC Health Services Research, 17. 339.

Hobson, E.V. orcid.org/0000-0002-8497-2338, Fazal, S., Shaw, P.J. orcid.org/0000-0002-8925-2567 et al. (1 more author) (2017) “Anything that makes life’s journey better.” Exploring the use of digital technology by people living with motor neurone disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 18 (5-6). pp. 378-387. ISSN 2167-8421

Pancani, S., Tindale, W., Shaw, P.J. et al. (2 more authors) (2017) An objective functional characterisation of head movement impairment in individuals with neck muscle weakness due to Amyotrophic lateral sclerosis. PLoS One, 12 (1). e0169019. ISSN 1932-6203

Hobson, E.V. orcid.org/0000-0002-8497-2338, Harwood, C.A., McDermott, C.J. orcid.org/0000-0002-1269-9053 et al. (1 more author) (2016) Clinical aspects of motor neurone disease. Medicine, 44 (9). pp. 552-556. ISSN 1357-3039

Hobson, E.V. and McDermott, C.J. orcid.org/0000-0002-1269-9053 (2016) Supportive and symptomatic management of amyotrophic lateral sclerosis. Nature Reviews Neurology, 12 (9). pp. 526-538. ISSN 1759-4758

McGeachan, A.J., Hobson, E.V., Al-Chalabi, A. et al. (19 more authors) (2016) A multicentre evaluation of oropharyngeal secretion management practices in amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener. ISSN 2167-8421

McDermott, C.J., Bradburn, M.J., Maguire, C. et al. (35 more authors) (2016) DiPALS: Diaphragm Pacing in patients with Amyotrophic Lateral Sclerosis - a randomised controlled trial. Health Technology Assessment, 20 (45). pp. 1-186. ISSN 1366-5278

Stavroulakis, T. and McDermott, C.J. orcid.org/0000-0002-1269-9053 (2016) Enteral feeding in neurological disorders. Practical Neurology. practneurol-2016. ISSN 1474-7758

Bury, J.J., Highley, J.R., Cooper-Knock, J. et al. (6 more authors) (2016) Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS. Neuropathology , 36 (2). pp. 125-134. ISSN 0919-6544

Harwood, C.A., Westgate, K., Gunstone, S. et al. (4 more authors) (2016) Long-term physical activity: an exogenous risk factor for sporadic amyotrophic lateral sclerosis? Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 17 (5-6). pp. 377-384. ISSN 2167-8421

Pancani, S., Rowson, J., Tindale, W. et al. (9 more authors) (2016) Assessment of the Sheffield Support Snood, an innovative cervical orthosis designed for people affected by neck muscle weakness. Clinical Biomechanics, 32. pp. 201-206. ISSN 1879-1271

Jenkins, T.M., Alix, J.J. orcid.org/0000-0001-8391-9749, Kandler, R.H. et al. (2 more authors) (2016) The role of cranial and thoracic EMG within diagnostic criteria for ALS. Muscle and Nerve. ISSN 0148-639X

McDermott, C.J., Shaw, P.J., Cooper, C.L. et al. (25 more authors) (2015) Safety and efficacy of diaphragm pacing in patients with respiratory insufficiency due to amyotrophic lateral sclerosis (DiPALS): a multicentre, open-label, randomised controlled trial. Lancet Neurology, 14 (9). pp. 883-892. ISSN 1474-4422

Rafiq, M.K., Lee, E., Bradburn, M. et al. (2 more authors) (2015) Effect of lipid profile on prognosis in the patients with amyotrophic lateral sclerosis: Insights from the olesoxime clinical trial. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 16 (7-8). pp. 478-484. ISSN 2167-8421

Rafiq, M.K., Bradburn, M., Proctor, A.R. et al. (4 more authors) (2015) A preliminary randomized trial of the mechanical insufflator-exsufflator versus breath-stacking technique in patients with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 16 (7-8). pp. 448-455. ISSN 2167-8421

McDermott, C.J., Shaw, P.J., Stavroulakis, T. et al. (24 more authors) (2015) Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study. Lancet Neurology, 14 (7). pp. 702-709. ISSN 1474-4422

Raman, R., Allen, S.P., Goodall, E.F. et al. (11 more authors) (2015) Gene expression signatures in motor neurone disease fibroblasts reveal dysregulation of metabolism, hypoxia-response and RNA processing functions. Neuropathology and Applied Neurobiology, 41 (2). pp. 201-226. ISSN 0305-1846

McGeachan, A.J., Hobson, E.V., Shaw, P.J. et al. (1 more author) (2014) Developing an outcome measure for excessive saliva management in MND and an evaluation of saliva burden in Sheffield. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 16 (1-2). pp. 108-113. ISSN 2167-8421

Kirby, J., Highley, J.R., Cox, L. et al. (8 more authors) (2013) Lack of unique neuropathology in amyotrophic lateral sclerosis associated with p.K54E angiogenin (ANG) mutation. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 39 (5). pp. 562-571. ISSN 0305-1846

Jenkins, T.M., Burness, C., Connolly, D.J. et al. (6 more authors) (2013) A prospective pilot study measuring muscle volumetric change in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration , 14 (5-6). 414 - 423. ISSN 2167-8421

McDermott, C.J., Maguire, C., Cooper, C.L. et al. (18 more authors) (2012) Protocol for diaphragm pacing in patients with respiratory muscle weakness due to motor neurone disease (DiPALS): a randomised controlled trial. BMC Neurology, 12. 74. ISSN 1471-2377

Besson, H., Harwood, C.A., Ekelund, U. et al. (4 more authors) (2010) Validation of the historical adulthood physical activity questionnaire (HAPAQ) against objective measurements of physical activity. International Journal of Behavioral Nutrition and Physical Activity, 7. 54. ISSN 1479-5868

Kirby, J., Goodall, E.F., Smith, W. et al. (10 more authors) (2010) Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis. Neurogenetics, 11 (2). pp. 217-225. ISSN 1364-6745