Diagnosis and management of motor neurone disease

Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity

Polazzi, E., Mengoni, I., Caprini, M., Peña‐Altamira, E., Kurtys, E., & Monti, B. (2012) · Neurosignals · doi:10.1159/000337115 · Cited by 9,023 · see citing works

Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

Neumann, M., Sampathu, D. M., Kwong, L. K., Truax, A. C., Micsenyi, M. C., Chou, T. T., Bruce, J., Schuck, T., Grossman, M., Clark, C. M., et al. (2006) · Science · doi:10.1126/science.1134108 · Cited by 6,576 · see citing works

Onset and Progression in Inherited ALS Determined by Motor Neurons and Microglia

Boillée, S., Yamanaka, K., Lobsiger, C. S., Copeland, N. G., Jenkins, N. A., Kassiotis, G., Kollias, G., & Cleveland, D. W. (2006) · Science · doi:10.1126/science.1123511 · Cited by 1,623 · see citing works

Dose-ranging study of riluzole in amyotrophic lateral sclerosis

Amyotrophic Lateral Sclerosis/Riluzole Study Group II, Lacomblez, L., Bensimon, G., Meininger, V., Leigh, P. N., & Guillet, P. (1996) · The Lancet · doi:10.1016/s0140-6736(96)91680-3 · Cited by 1,303 · see citing works

Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons

Nagai, M., Re, D. B., Nagata, T., Chalazonitis, A., Jessell, T. M., Wichterle, H., & Przedborski, S. (2007) · Nature Neuroscience · doi:10.1038/nn1876 · Cited by 1,220 · see citing works

Effects of non-invasive ventilation on survival and quality of life in patients with amyotrophic lateral sclerosis: a randomised controlled trial

Bourke, S. C., Tomlinson, M., Williams, T. L., Bullock, R., Shaw, P. J., & Gibson, G. J. (2006) · The Lancet Neurology · doi:10.1016/s1474-4422(05)70326-4 · Cited by 1,170 · see citing works

Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND)

Miller, R. G., Mitchell, J. D., & Moore, D. H. (2012) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd001447.pub3 · Cited by 1,123 · see citing works

Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND)

Miller, R. G., Jd, M., Lyon, M., & Moore, D. (2002) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd001447 · Cited by 910 · see citing works

Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996-2000

Traynor, B. J. (2003) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.74.9.1258 · Cited by 493 · see citing works

Nutritional status is a prognostic factor for survival in ALS patients

Desport, J. C., Preux, P., Truong, T., Vallat, J. M., Sautereau, D., & Couratier, P. (1999) · Neurology · doi:10.1212/wnl.53.5.1059 · Cited by 486 · see citing works

Oxidative stress in ALS: A mechanism of neurodegeneration and a therapeutic target

Barber, S. C., Mead, R. J., & Shaw, P. J. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2006.03.008 · Cited by 475 · see citing works

Nutritional status of patients with amyotrophic lateral sclerosis: relation to the proximity of death

Kasarskis, E. J., Berryman, S., Vanderleest, J. G., Schneider, A., & McClain, C. J. (1996) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/63.1.130 · Cited by 293 · see citing works

EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relatives

Andersen, P. M., Borasio, G. D., Dengler, R., Hardiman, O. M., Kollewe, K., Leigh, P. N., Pradat, P., Silani, V., & Tomik, B. (2005) · European Journal of Neurology · doi:10.1111/j.1468-1331.2005.01351.x · Cited by 290 · see citing works

The epidemiology of motor neuron diseases: a review of recent studies

Worms, P. (2001) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(01)00630-x · Cited by 278 · see citing works

Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis

Jiang, Y., Yamamoto, M., Kobayashi, Y., Yoshihara, T., Liang, Y., Terao, S., Takeuchi, H., Ishigaki, S., Katsuno, M., Adachi, H., et al. (2005) · Annals of Neurology · doi:10.1002/ana.20379 · Cited by 255 · see citing works

Whole-Genome Analysis of Sporadic Amyotrophic Lateral Sclerosis

Dunckley, T., Huentelman, M. J., Craig, D. W., Pearson, J. V., Szelinger, S., Joshipura, K., Halperin, R. F., Stamper, C., Jensen, K. R., Letizia, D., et al. (2007) · New England Journal of Medicine · doi:10.1056/nejmoa070174 · Cited by 236 · see citing works

Stem cell treatment in Amyotrophic Lateral Sclerosis

Mazzini, L., Mareschi, K., Ferrero, I., Vassallo, E., Oliveri, G., Nasuelli, N. A., Oggioni, G. D., Testa, L., & Fagioli, F. (2007) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2007.05.016 · Cited by 227 · see citing works

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

Schymick, J. C., Scholz, S. W., Fung, H., Britton, A. F., Arepalli, S., Gibbs, J. R., Lombardo, F., Matarín, M., Kasperavičiūtė, D., Hernandez, D. G., et al. (2007) · The Lancet Neurology · doi:10.1016/s1474-4422(07)70037-6 · Cited by 218 · see citing works

Microarray Analysis of the Cellular Pathways Involved in the Adaptation to and Progression of Motor Neuron Injury in the SOD1 G93A Mouse Model of Familial ALS

Ferraiuolo, L., Heath, P. R., Holden, H. M., Kasher, P. R., Kirby, J., & Shaw, P. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1470-07.2007 · Cited by 198 · see citing works

Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004

O’Toole, O., Traynor, B. J., Brennan, P., Sheehan, C., Frost, E., Corr, B., & Hardiman, O. M. (2007) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2007.117788 · Cited by 192 · see citing works

Motor neurone disease: a hospice perspective.

O’Brien, T., Kelly, M. J., & Saunders, C. (1992) · BMJ · doi:10.1136/bmj.304.6825.471 · Cited by 175 · see citing works

Amyotrophic Lateral Sclerosis: Enteral Nutrition Provision—Endoscopic or Radiologic Gastrostomy?

Thornton, F. J., Fotheringham, T., Alexander, M. D., Hardiman, O. M., McGrath, F. P., & Lee, M. J. (2002) · Radiology · doi:10.1148/radiol.2243010909 · Cited by 130 · see citing works

The Scottish Motor Neuron Disease Register: a prospective study of adult onset motor neuron disease in Scotland. Methodology, demography and clinical features of incident cases in 1989.

(1992) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.55.7.536 · Cited by 121 · see citing works

Antioxidant treatment for amyotrophic lateral sclerosis or motor neuron disease

Orrell, R. W., Lane, R. J., & Ross, M. (2007) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd002829.pub4 · Cited by 98 · see citing works

Breaking the news in amyotrophic lateral sclerosis

Borasio, G. D. (1998) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(98)00211-1 · Cited by 92 · see citing works

Motor neuron disorders

Shaw, P. J., & Strong, M. J. (2003) · Cited by 51 · see citing works

ALS: life and death in a bad neighborhood

Monk, P. N., & Shaw, P. J. (2006) · Nature Medicine · doi:10.1038/nm0806-885 · Cited by 45 · see citing works

Chapter 4 Molecular mechanisms of motor neuron degeneration in amyotrophic lateral sclerosis

Barber, S. C., & Shaw, P. J. (2007) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)80007-8 · Cited by 3 · see citing works

Gene expression signatures in motor neurone disease fibroblasts reveal dysregulation of metabolism, hypoxia‐response and RNA processing functions

Raman, R., Allen, S. P., Goodall, G., Kramer, S., Ponger, L., Heath, P. R., Milo, M., Hollinger, H. C., Walsh, T., Highley, J. R., et al. (2014) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12147 · Cited by 254 · see citing works

Neuronal dark matter: the emerging role of microRNAs in neurodegeneration

Goodall, E. F., Heath, P. R., Bandmann, O., Kirby, J., & Shaw, P. J. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00178 · Cited by 187 · see citing works

Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study

ProGas Study Group (2015) · The Lancet Neurology · doi:10.1016/s1474-4422(15)00104-0 · Cited by 165 · see citing works

The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype

Cooper‐Knock, J., Shaw, P. J., & Kirby, J. (2014) · Acta Neuropathologica · doi:10.1007/s00401-014-1251-9 · Cited by 163 · see citing works

A 10-year literature review of family caregiving for motor neurone disease: Moving from caregiver burden studies to palliative care interventions

Aoun, S. M., Bentley, B., Funk, L., Toye, C., Grande, G., & Stajduhar, K. J. (2013) · Palliative Medicine · doi:10.1177/0269216312455729 · Cited by 152 · see citing works

Identifying who will benefit from non-invasive ventilation in amyotrophic lateral sclerosis/motor neurone disease in a clinical cohort

Berlowitz, D. J., Howard, M. E., Fiore, J. F., Hoorn, S. V., O’Donoghue, F. J., Westlake, J., Smith, A. M., Beer, F., Mathers, S., & Talman, P. S. (2015) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2014-310055 · Cited by 152 · see citing works

Serum miRNAs miR-206, 143-3p and 374b-5p as potential biomarkers for amyotrophic lateral sclerosis (ALS)

Waller, R., Goodall, G., Milo, M., Cooper‐Knock, J., Costa, M. D., Hobson, E., Kazoka, M., Wollff, H., Heath, P. R., Shaw, P. J., et al. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.03.027 · Cited by 148 · see citing works

Novel FUS/TLS Mutations and Pathology in Familial and Sporadic Amyotrophic Lateral Sclerosis

Hewitt, C., Kirby, J., Highley, J. R., Hartley, J. A., Hibberd, R., Hollinger, H. C., Williams, T. L., Ince, P. G., McDermott, C. J., & Shaw, P. J. (2010) · Archives of Neurology · doi:10.1001/archneurol.2010.52 · Cited by 139 · see citing works

Identification of a circulating miRNA signature in extracellular vesicles collected from amyotrophic lateral sclerosis patients

Saucier, D., Wajnberg, G., Roy, J. W., Beauregard, A., Chacko, S. M., Crapoulet, N., Fournier, S., Ghosh, A., Lewis, S. M., Marrero, A., et al. (2018) · Brain Research · doi:10.1016/j.brainres.2018.12.016 · Cited by 134 · see citing works

Biographical disruption, abruption and repair in the context of Motor Neurone Disease

Locock, L., Ziébland, S., & Dumelow, C. (2009) · Sociology of Health & Illness · doi:10.1111/j.1467-9566.2009.01176.x · Cited by 132 · see citing works

An evaluation of neurophysiological criteria used in the diagnosis of motor neuron disease

Douglass, C., Kandler, R., Shaw, P. J., & McDermott, C. J. (2010) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2009.197434 · Cited by 119 · see citing works

Brown-Vialetto-Van Laere syndrome

Sathasivam, S. (2008) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-3-9 · Cited by 108 · see citing works

From symptom onset to a diagnosis of amyotrophic lateral sclerosis/motor neuron disease (ALS/MND): Experiences of people with ALS/MND and family carers – a qualitative study

O'Brien, M. R., Whitehead, B. A., Jack, B., & Mitchell, J. D. (2011) · Amyotrophic Lateral Sclerosis · doi:10.3109/17482968.2010.546414 · Cited by 106 · see citing works

‘All in the same boat’? Patient and carer attitudes to peer support and social comparison in Motor Neurone Disease (MND)

Locock, L., & Brown, J. (2010) · Social Science & Medicine · doi:10.1016/j.socscimed.2010.06.043 · Cited by 105 · see citing works

Neurodegenerative diseases linked to misfolded proteins and their therapeutic approaches: A review

Khanam, H., Ali, A., Asif, M., & Shamsuzzaman (2016) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2016.08.006 · Cited by 100 · see citing works

Peripheral Glycolysis in Neurodegenerative Diseases

Bell, S., Burgess, T., Lee, J., Blackburn, D. J., Allen, S. P., & Mortiboys, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21238924 · Cited by 83 · see citing works

The Emerging Role of MitomiRs in the Pathophysiology of Human Disease

Duarte, F. V., Palmeira, C. M., & Rolo, A. P. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-22671-2_8 · Cited by 81 · see citing works

Being differently the same: The mediation of identity tensions in the sharing of illness experiences

Mazanderani, F., Locock, L., & powell, J. A. (2011) · Social Science & Medicine · doi:10.1016/j.socscimed.2011.10.036 · Cited by 76 · see citing works

The Omega-3 Fatty Acid Eicosapentaenoic Acid Accelerates Disease Progression in a Model of Amyotrophic Lateral Sclerosis

Yip, P. K., Pizzasegola, C., Gladman, S. J., Biggio, M. L., Marino, M., Jayasinghe, M., Ullah, F., Dyall, S. C., Malaspina, A., Bendotti, C., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061626 · Cited by 69 · see citing works

The latest progress on miR‐374 and its functional implications in physiological and pathological processes

Bian, H., Zhou, Y., Zhou, D., Zhang, Y., Shang, D., & Qi, J. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14219 · Cited by 67 · see citing works

Feasibility, Acceptability, and Potential Effectiveness of Dignity Therapy for People with Motor Neurone Disease

Bentley, B., O’Connor, M., Kane, R. T., & Breen, L. J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096888 · Cited by 64 · see citing works

Creatine kinase enzyme level correlates positively with serum creatinine and lean body mass, and is a prognostic factor for survival in amyotrophic lateral sclerosis

Rafiq, M. K., Lee, E. C., Bradburn, M. J., McDermott, C. J., & Shaw, P. J. (2016) · European Journal of Neurology · doi:10.1111/ene.12995 · Cited by 64 · see citing works

Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives

Faravelli, I., Bucchia, M., Rinchetti, P., Nizzardo, M., Simone, C., Frattini, E., & Corti, S. P. (2014) · Stem Cell Research & Therapy · doi:10.1186/scrt476 · Cited by 61 · see citing works

Factors influencing decision-making in relation to timing of gastrostomy insertion in patients with motor neurone disease

Stavroulakis, T., Baird, W. O., Baxter, S. K., Walsh, T., Shaw, P. J., & McDermott, C. J. (2013) · BMJ Supportive & Palliative Care · doi:10.1136/bmjspcare-2013-000497 · Cited by 60 · see citing works

Oligodendrocyte pathology exceeds axonal pathology in white matter in human amyotrophic lateral sclerosis

Lorente Pons, A., Higginbottom, A., Cooper‐Knock, J., Alrafiah, A., Alofi, E., Kirby, J., Shaw, P. J., Wood, J. D., & Highley, J. R. (2020) · The Journal of Pathology · doi:10.1002/path.5455 · Cited by 57 · see citing works

Motor neurone disease: progress and challenges

Dharmadasa, T., Henderson, R. D., Talman, P. S., Macdonell, R. A. L., Mathers, S., Schultz, D. W., Needham, M., Zoing, M. C., Vucic, S., & Kiernan, M. C. (2017) · The Medical Journal of Australia · doi:10.5694/mja16.01063 · Cited by 60 · see citing works

Effect of lipid profile on prognosis in the patients with amyotrophic lateral sclerosis: Insights from the olesoxime clinical trial

Rafiq, M. K., Lee, E. C., Bradburn, M. J., McDermott, C. J., & Shaw, P. J. (2015) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2015.1062517 · Cited by 58 · see citing works

The use of non-invasive ventilation at end of life in patients with motor neurone disease: A qualitative exploration of family carer and health professional experiences

Baxter, S. K., Baird, W. O., Thompson, S., Bianchi, S. M., Walters, S. J., Lee, E. C., Ahmedzai, S. H., Proctor, A., Shaw, P. J., & McDermott, C. J. (2013) · Palliative Medicine · doi:10.1177/0269216313478449 · Cited by 57 · see citing works

The TiM system: developing a novel telehealth service to improve access to specialist care in motor neurone disease using user-centered design

Hobson, E., Baird, W. O., Partridge, R., Cooper, C. L., Mawson, S., Quinn, A., Shaw, P. J., Walsh, T., Wolstenholme, D., & McDermott, C. J. (2018) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.1080/21678421.2018.1440408 · Cited by 56 · see citing works

Activation of ER Stress and Autophagy Induced by TDP-43 A315T as Pathogenic Mechanism and the Corresponding Histological Changes in Skin as Potential Biomarker for ALS with the Mutation

Wang, X., Zhou, S. Y., Ding, X., Ma, M., Zhang, J., Zhou, Y., Wu, E., & Teng, J. (2015) · International Journal of Biological Sciences · doi:10.7150/ijbs.12657 · Cited by 55 · see citing works

Neurogenic Bowel Dysfunction in Children and Adolescents

Mosiello, G., Safder, S., Marshall, D. C., Rolle, U., & Benninga, M. A. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10081669 · Cited by 53 · see citing works

The impact of gastrostomy in motor neurone disease: challenges and benefits from a patient and carer perspective

Stavroulakis, T., Baird, W. O., Baxter, S. K., Walsh, T., Shaw, P. J., & McDermott, C. J. (2014) · BMJ Supportive & Palliative Care · doi:10.1136/bmjspcare-2013-000609 · Cited by 52 · see citing works

Feasibility, acceptability and potential effectiveness of dignity therapy for family carers of people with motor neurone disease

Bentley, B., O’Connor, M., Breen, L. J., & Kane, R. (2014) · BMC Palliative Care · doi:10.1186/1472-684x-13-12 · Cited by 46 · see citing works

Patient journey to a specialist amyotrophic lateral sclerosis multidisciplinary clinic: an exploratory study

Galvin, M., Madden, C., Maguire, S., Heverin, M., Vajda, A., Staines, A. S., & Hardiman, O. M. (2015) · BMC Health Services Research · doi:10.1186/s12913-015-1229-x · Cited by 45 · see citing works

A multicentre evaluation of oropharyngeal secretion management practices in amyotrophic lateral sclerosis

McGeachan, A. J., Hobson, E., Al‐Chalabi, A., Stephenson, J., Chandran, S., Crawley, F., Dick, D. J., Donaghy, C. G., Ellis, C., Gorrie, G., et al. (2016) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.1080/21678421.2016.1221433 · Cited by 44 · see citing works

Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP‐43‐negative inclusions of C9ORF72‐ALS

Bury, J. J., Highley, J. R., Cooper‐Knock, J., Goodall, G., Higginbottom, A., McDermott, C. J., Ince, P. G., Shaw, P. J., & Kirby, J. (2015) · Neuropathology · doi:10.1111/neup.12240 · Cited by 44 · see citing works

Enteral feeding in neurological disorders

Stavroulakis, T., & McDermott, C. J. (2016) · Practical Neurology · doi:10.1136/practneurol-2016-001408 · Cited by 43 · see citing works

Gender, risk assessment, and political ambition

Sweet-Cushman, J. (2016) · Politics and the Life Sciences · doi:10.1017/pls.2016.13 · Cited by 42 · see citing works

The Interplay Between Neuroinfections, the Immune System and Neurological Disorders: A Focus on Africa

Ngarka, L., Fodjo, J. N. S., Aly, E., Masocha, W., & NJAMNSHI, A. K. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.803475 · Cited by 44 · see citing works

Membrane compartments and purinergic signalling: P2X receptors in neurodegenerative and neuroinflammatory events

Apolloni, S., Montilli, C., Finocchi, P., & Amadio, S. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06796.x · Cited by 41 · see citing works

From first symptoms to diagnosis of amyotrophic lateral sclerosis: perspectives of an Irish informal caregiver cohort—a thematic analysis

Galvin, M., Gaffney, R., Corr, B., Mays, I., & Hardiman, O. M. (2017) · BMJ Open · doi:10.1136/bmjopen-2016-014985 · Cited by 37 · see citing works

Planning for an uncertain future in progressive neurological disease: a qualitative study of patient and family decision-making with a focus on eating and drinking

Clarke, G., Fistein, E., Holland, A. J., Tobin, J., Barclay, S., & Barclay, S. I. G. (2018) · BMC Neurology · doi:10.1186/s12883-018-1112-6 · Cited by 37 · see citing works

Using telehealth in motor neuron disease to increase access to specialist multidisciplinary care: a UK-based pilot and feasibility study

Hobson, E., Baird, W. O., Bradburn, M. J., Cooper, C. L., Mawson, S., Quinn, A., Shaw, P. J., Walsh, T., & McDermott, C. J. (2019) · BMJ Open · doi:10.1136/bmjopen-2018-028525 · Cited by 36 · see citing works

Therapeutic effects of percutaneous endoscopic gastrostomy on survival in patients with amyotrophic lateral sclerosis: A meta-analysis

Cui, F., Sun, L., Xiong, J., Li, J., Zhao, Y., & Huang, X. (2018) · PLoS ONE · doi:10.1371/journal.pone.0192243 · Cited by 34 · see citing works

Caregivers of People with Neurodegenerative Diseases: Profile and Unmet Needs from a Population-Based Survey in South Australia

Aoun, S. M., McConigley, R., Abernethy, A. P., & Currow, D. C. (2010) · Journal of Palliative Medicine · doi:10.1089/jpm.2009.0318 · Cited by 34 · see citing works

The role of RNA processing in the pathogenesis of motor neuron degeneration

Bäumer, D., Ansorge, O., Almeida, M., & Talbot, K. (2010) · Expert Reviews in Molecular Medicine · doi:10.1017/s1462399410001523 · Cited by 33 · see citing works

Process evaluation and exploration of telehealth in motor neuron disease in a UK specialist centre

Hobson, E., Baird, W. O., Bradburn, M. J., Cooper, C. L., Mawson, S., Quinn, A., Shaw, P. J., Walsh, T., & McDermott, C. J. (2019) · BMJ Open · doi:10.1136/bmjopen-2018-028526 · Cited by 31 · see citing works

Head-Up; An interdisciplinary, participatory and co-design process informing the development of a novel head and neck support for people living with progressive neck muscle weakness

Reed, H., Langley, J., Stanton, A., Heron, N., Clarke, Z., Judge, S., McCarthy, A. D., Squire, G., Quinn, A., Wells, O., et al. (2015) · Journal of Medical Engineering & Technology · doi:10.3109/03091902.2015.1088092 · Cited by 32 · see citing works

Tandem Repeat Polymorphisms

Hannan, A. J. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-5434-2_1 · Cited by 32 · see citing works

Considerations on the concept, definition, and diagnosis of amyotrophic lateral sclerosis

Xu, R., & Yuan, M. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.306065 · Cited by 30 · see citing works

Health care professionals’ views on psychological factors affecting nutritional behaviour in people with motor neuron disease: A thematic analysis

Zarotti, N., Coates, E. J., McGeachan, A. J., Williams, I. A., Beever, D., Hackney, G., Norman, P. E., Stavroulakis, T., White, D. A., White, S., et al. (2019) · British Journal of Health Psychology · doi:10.1111/bjhp.12388 · Cited by 28 · see citing works

Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease

Jenkins, T. M., Alix, J. J. P., Fingret, J., Esmail, T., Hoggard, N., Baster, K., McDermott, C. J., Wilkinson, I. D., & Shaw, P. J. (2019) · Journal of Neurology · doi:10.1007/s00415-019-09580-x · Cited by 26 · see citing works

Therapeutic opportunities and challenges of induced pluripotent stem cells-derived motor neurons for treatment of amyotrophic lateral sclerosis and motor neuron disease

Jaiswal, M. K. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.206635 · Cited by 27 · see citing works

Using transcutaneous carbon dioxide monitor (TOSCA 500) to detect respiratory failure in patients with amyotrophic lateral sclerosis: A validation study

Rafiq, M. K., Bradburn, M. J., Proctor, A., Billings, C., Bianchi, S. M., McDermott, C. J., & Shaw, P. J. (2012) · Amyotrophic Lateral Sclerosis · doi:10.3109/17482968.2012.688836 · Cited by 27 · see citing works

Prognostic factors and survival of ALS patients from Belgrade, Serbia

Stević, Z., Kostic-Dedic, S., Perić, S., Dedić, V., Basta, I. Z., Rakočević-Stojanović, V., & Lavrnić, D. (2016) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.1080/21678421.2016.1195410 · Cited by 27 · see citing works

Factors influencing decisions people with motor neuron disease make about gastrostomy placement and ventilation: A qualitative evidence synthesis

White, S., O’Cathain, A., Halliday, V., Croot, L., & McDermott, C. J. (2023) · Health Expectations · doi:10.1111/hex.13786 · Cited by 25 · see citing works

The nutritional management of people living with amyotrophic lateral sclerosis: A national survey of dietitians

White, S., Zarotti, N., Beever, D., Bradburn, M. J., Norman, P. E., Coates, E. J., Stavroulakis, T., White, D. A., McGeachan, A. J., Williams, I. A., et al. (2021) · Journal of Human Nutrition and Dietetics · doi:10.1111/jhn.12900 · Cited by 23 · see citing works

A novel passive neck orthosis for patients with degenerative muscle diseases: Development & evaluation

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