Cited by 221Amyotrophic Lateral Sclerosis ResearchNeurogenetic and Muscular Disorders ResearchPeripheral Neuropathies and Disorders

The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.

Diagnosis and management of motor neurone disease

Open access

McDermott, Christopher J, Shaw, Pamela J·2008·BMJ

DOI 10.1136/bmj.39493.511759.bePMC PMC2270983

Open this paper in CoChat — free account

Abstract

Motor neurone disease is a devastating illness which leads to progressive paralysis and eventual death. We will discuss the presentation of motor neurone disease in primary care and update non-specialists on progress with regards to life prolonging interventions, better control of disease symptoms, and an increased understanding of disease mechanisms. Motor neurone disease is rare but patients often are aware of it, so this review should help non-specialists reassure patients in whom it is unlikely to be the diagnosis.

Integrity signals

Registry

Crossref · 10.1136/bmj.39493.511759.be

Cites

28 of 28 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

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
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
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
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
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
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
Self-citation
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
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
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
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 489
Self-citation

Show all 28 references

Sorted by citations

Items 101–200 of 221

Kennedy’s Disease
Zajac, J. D., & Fui, M. N. T. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-5434-2_10 · Cited by 8
Understanding Quality of Life for People with Motor Neurone Disease Who Use Tracheostomy Ventilation and Family Members: A Scoping Review
Turner, N., Faull, C., Palmer, J., Armstrong, A., Bedford, J., Turner, M. R., & Wilson, E. (2024) · Brain Sciences · doi:10.3390/brainsci14080821 · Cited by 7
Fit for purpose? A cross-sectional study to evaluate the acceptability and usability of HeadUp, a novel neck support collar for neurological neck weakness
Sproson, L., Lanfranchi, V., Collins, A., Chhetri, S. K., Daly, N., Ennis, M., Glennon, L., Gorrie, G., Jay, E., Marsden, R., et al. (2020) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.1080/21678421.2020.1813308 · Cited by 7
Self-citation
A Case-Study Survey of an Eight-year Cluster of Motor Neurone Disease (MND) Referrals in a Rural English Village: Exploring Possible Aetiological Influences in a Hypothesis Stimulating Study
Pritchard, A. S. C. (2013) · Journal of Neurological Disorders · doi:10.4172/2329-6895.1000147 · Cited by 7
AMYOTROPHIC LATERAL SCLEROSIS : A REVIEW
Bansal, M., Singhvi, I. J., & Rajpurohit, R. (2024) · International Journal of Medicine & Health Research (IJMHR) · doi:10.71393/5e8v8h62 · Cited by 7
Epidemiology, disease evolution and economic burden of amyotrophic lateral sclerosis in France using the French national health data system
Corcia, P., Stenson, K., Doutriaux, A., Hadjrabia, H., Boer, F., Issa, S., Marguet, S., Bernard, F., Nasanbat, E., Nowacki, G., et al. (2025) · Brain Communications · doi:10.1093/braincomms/fcaf292 · Cited by 6
Specialist referrals and diagnostic delays in motor neurone disease: Mapping patients’ journey through hoops and hurdles in healthcare
Reynolds, S. J., & Chhetri, S. K. (2024) · Clinical Medicine · doi:10.1016/j.clinme.2024.100228 · Cited by 7
Eye-motion detection system for mnd patients
Xu, C.-L., & Lin, C. (2017) · International Conference on Soft Computing & Machine Intelligence (ISCMI) · doi:10.1109/iscmi.2017.8279606 · Cited by 6
Identifying key signs of motor neurone disease in primary care: a nested case–control study using the QResearch database
Mei, X. W., Burchardt, J., Ranger, T. A., McDermott, C. J., Radunović, A., Coupland, C. A. C., & Hippisley‐Cox, J. (2022) · BMJ Open · doi:10.1136/bmjopen-2021-058383 · Cited by 6
Self-citation
A critical view of the use of predictive energy equations for the identification of hypermetabolism in motor neuron disease: A pilot study
Roscoe, S., Skinner, E., Kibirige, E. K., Childs, C., Weekes, C. E., Wootton, S. A., Allen, S. P., McDermott, C. J., & Stavroulakis, T. (2023) · Clinical Nutrition ESPEN · doi:10.1016/j.clnesp.2023.08.017 · Cited by 6
Self-citation
Caregiver suctioning education for Japanese patients with an invasive home ventilator
Imaiso, J., & Yamauchi, T. (2009) · Nursing and Health Sciences · doi:10.1111/j.1442-2018.2009.00469.x · Cited by 6
Boldine as a neuroprotective agent against motor neuron degeneration in models of amyotrophic lateral sclerosis
Toro, C. A., Zhao, W., Silva, P. G., Retamal-Santibáñez, D., Rojas, F., Pan, J., Johnson, N., Duarte, Y., Cardozo, C. P., Sáez, J. C., et al. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1640590 · Cited by 5
Factors associated with assistive technology prescription and acceptance in motor neurone disease
Connolly, A., Bailey, S., Lamont, R., & Tu, A. (2023) · Disability and Rehabilitation Assistive Technology · doi:10.1080/17483107.2023.2272858 · Cited by 6
Genetic testing and reproductive choice in neurological disorders
Lee, O., & Porteous, M. E. (2017) · Practical Neurology · doi:10.1136/practneurol-2017-001619 · Cited by 5
Oral Treatment with RD2RD2 Impedes Development of Motoric Phenotype and Delays Symptom Onset in SOD1G93A Transgenic Mice
Post, J., Schaffrath, A., Gering, I., Hartwig, S., Lehr, S., Shah, N. J., Langen, K., Willbold, D., Kutzsche, J., & Willuweit, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137066 · Cited by 4
A Y374X TDP43 truncation leads to an altered metabolic profile in amyotrophic lateral sclerosis fibroblasts driven by pyruvate and TCA cycle intermediate alterations
Allen, S. P., Sultan, A. A., Kibirige, E. K., Tonkiss, E., Hamer, K. J., Castelli, L. M., Lin, Y.-H., Roscoe, S., Stefanidis, N., Mead, R. J., et al. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1151848 · Cited by 4
Self-citation
An ‘Acute’ Presentation of Motor Neuron Disease
Lad, T. S. (2011) · Acute Medicine Journal · doi:10.52964/amja.0494 · Cited by 4
Characterization of the nigroestriatal system in a sample of patients with amyotrophic lateral sclerosis
Monsalve, C. A. J., Fornari, L. H. T., Júnior, N. D. S., Nakata, D., Neto, E. G. D. C., Rotta, F. T., & Rieder, C. R. D. M. (2022) · Arquivos de Neuro-Psiquiatria · doi:10.1055/s-0042-1755282 · Cited by 4
The NIHR Invention for Innovation (i4i) Programme: A Review of Progress and Contributions to Innovation in Healthcare Technologies
Marjanovic, S., Krapels, J., Sousa, S., Castle‐Clarke, S., Horváth, V., & Chataway, J. (2015) · Rand health quarterly · doi:10.7249/rhq-05-02-04 · Cited by 4
A NSC ‐34 cell line‐derived spheroid model: Potential and challenges for in vitro evaluation of neurodegeneration
Arnaldi, P., Casarotto, E., Relucenti, M., Bellese, G., Gagliani, M. C., Crippa, V., Castagnola, P., & Cortese, K. (2024) · Microscopy Research and Technique · doi:10.1002/jemt.24651 · Cited by 3
Randomised controlled trial with parallel process evaluation and health economic analysis to evaluate a nutritional management intervention, OptiCALS, for patients with amyotrophic lateral sclerosis: study protocol
Peace, A., White, D. A., Hackney, G., Bradburn, M. J., Norman, P. E., White, S., Al‐Chalabi, A., Baird, W. O., Beever, D., Cade, J. E., et al. (2025) · BMJ Open · doi:10.1136/bmjopen-2024-096098 · Cited by 3
Self-citation
When months matter; modelling the impact of the COVID-19 pandemic on the diagnostic pathway of Motor Neurone Disease (MND)
Burchill, E., Rawji, V., Styles, K., Rooney, S., Stone, P. C., Astin, R., & Sharma, N. (2023) · PLoS ONE · doi:10.1371/journal.pone.0259487 · Cited by 3
The need to consider ‘temporality’ in person‐centred care of people with motor neurone disease
Harris, D., Jack, K., & Wibberley, C. (2023) · Journal of Evaluation in Clinical Practice · doi:10.1111/jep.13854 · Cited by 3
Sensory Changes Related to Swallowing in Motor Neurone Disease
Paterson, M., Doeltgen, S., & Francis, R. L. (2024) · Dysphagia · doi:10.1007/s00455-024-10742-x · Cited by 4
Nutritional Support in Amyotrophic Lateral Sclerosis
Stavroulakis, T., & McDermott, C. J. (2017) · Springer eBooks · doi:10.1007/978-3-319-53171-7_6 · Cited by 3
Self-citation
Narcolepsy, cataplexy, hypocretin and co-existing other health complaints: A review
Gauci, S., Hosking, W., & Bruck, D. (2017) · Cogent Medicine · doi:10.1080/2331205x.2017.1312791 · Cited by 3
Gait variability assessment in neuro-degenerative patients by measuring complexity of independent sources
Heydarzadeh, M., Tan, C., Nourani, M., & Ostadabbas, S. (2017) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2017.8037534 · Cited by 3
Testing motor grounding and somatotopic effects for literal and figurative action language in motor neuron diseases: a between-group and multiple-case analysis
Frau, F., Diamanti, L., Pompei, C., Bischetti, L., Losi, G., Coppa, G., Tonini, E., Bettoni, V., Canal, P., Ceroni, M., et al. (2026) · Language Cognition and Neuroscience · doi:10.1080/23273798.2026.2645977 · Cited by 2
Targeting lipid nanoparticle mediated co-delivery of edaravone and kaempferol for amyotrophic lateral sclerosis therapy
tian, J., Jin, Z., chi, Y. K., Wang, P., & Sun, H. (2026) · Nanoscale · doi:10.1039/d6nr00300a · Cited by 2
Motor neuron disease mimics in practice: a case series
Aitchison, C., Romanowski, C. A. J., Barker, A., & Jenkins, T. M. (2022) · BMJ Case Reports · doi:10.1136/bcr-2021-247441 · Cited by 2
Understanding motor neurone disease
Gent, C. (2012) · Nursing and Residential Care · doi:10.12968/nrec.2012.14.12.646 · Cited by 2
Chaos Based Quantitative Electro-Diagnostic Marker for Diagnosis of Myopathy, Neuropathy and Motor Neuron Disease
Ghosh, D. C., Dutta, S., Chakraborty, S., & Samanta, S. (2017) · Journal of Neurology and Neuroscience · doi:10.21767/2171-6625.1000226 · Cited by 2
Psychosocial Interventions in Dementia
Kiridoshi, A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.019 · Cited by 2
Review of Treatment for Late-Life Depression
Hay, K., Stageman, W., & Allan, C. L. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.021 · Cited by 2
O cuidado de enfermagem ao portador de Esclerose Lateral Amiotrófica: uma revisão integrativa
de Omena, I. C. A., Brandão, L. D. S., Albuquerque, J. D. M., Comassetto, I., Nagliate, P. D. C., Alves, K. D. M. C., & Salles, I. D. A. C. M. (2019) · Enfermagem Brasil · doi:10.33233/eb.v17i6.2099 · Cited by 2
Existential loss in the context of Motor Neurone Disease: A hermeneutic phenomenological study
Harris, D. (2015) · doi:10.7490/f1000research.1111184.1 · Cited by 2
Managing a patient with a rapidly progressing neurodegenerative condition
Ramaswamy, B., & Sheppard, A. (2010) · International Journal of Therapy and Rehabilitation · doi:10.12968/ijtr.2010.17.6.48155 · Cited by 1
Palliative and End-of-Life Oral Care and Oral Care Planning
Fitzgerald, R., & Geddis‐Regan, A. (2022) · BDJ clinician's guides · doi:10.1007/978-3-031-10224-0_11 · Cited by 1
Does carer psychological inflexibility moderate the relationship between motor neurone disease symptomatology and carer anticipatory grief emotions?
Trucco, A. P., Khondoker, M. R., Kishita, N., Backhouse, T., Meuser, T. M., & Mioshi, E. (2025) · Journal of Health Psychology · doi:10.1177/13591053251328490 · Cited by 1
A Systematic Review of Attributes Influencing Preferences for Treatments and Interventions in People With Amyotrophic Lateral Sclerosis ( ALS )
Clift, A., Rowen, D., Knox, L., Griffiths, A. W., & McDermott, C. J. (2025) · Muscle & Nerve · doi:10.1002/mus.28437 · Cited by 1
Self-citation
Diagnosis of Australasian Patients with Neuromuscular Disease
Scriba, C. K., Faiz, F., Black, M., Gooding, R., Sivadorai, P., Trajanoski, D., Botero, A., Wise, C., Ravenscroft, G., Davis, M. R., et al. (2025) · Journal of Molecular Diagnostics · doi:10.1016/j.jmoldx.2025.03.011 · Cited by 1
Xenotransplantation of Human Umbilical Mesenchymal Stromal Cells Derived from Wharton's Jelly Mitigates Mouse Amyotrophic Lateral Sclerosis
Lin, C., Chen, Y., Yeh, C., Hsu, S. P. C., & Fu, Y.-S. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04485-1 · Cited by 1
Identifying priorities for a national motor neurone disease (amyotrophic lateral sclerosis) guideline: results from an Australian online survey
Fragkoudi, A., Stern, C., Pollock, D., Barker, T. H., Semendric, I., Labra, J., Vucic, S., Whitehouse, J., & Munn, Z. (2026) · Disability and Rehabilitation · doi:10.1080/09638288.2026.2643544 · Cited by 1
Diaphragm pacing systems for amyotrophic lateral sclerosis / motor neuron disease
Maguire, C., McDermott, C. J., Hind, D., Radunović, A., & Shaw, P. J. (2014) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd011222 · Cited by 1
Self-citation
Existential concerns for people with motor neurone disease: Who is listening to their needs, priorities and preferences?
Harris, D. (2016) · British Journal of Occupational Therapy · doi:10.1177/0308022615616975 · Cited by 1
Pain in motor neurone disease
Clarke, J. (2016) · British Journal of Neuroscience Nursing · doi:10.12968/bjnn.2016.12.2.85 · Cited by 1
Palliative care in non-malignant neurological disease
Watson, M., Lucas, C. F., Hoy, A., & Wells, J. (2009) · doi:10.1093/med/9780199234356.003.0029 · Cited by 1
Exploring reasons for declining and withdrawing from non-invasive ventilation among motor neurone disease patients : an interpretative phenomenological analysis
Ando, H. (2019) · University of Liverpool · doi:10.17638/03061722 · Cited by 1
Genetik der amyotrophen Lateralsklerose
Czell, D. (2019) · Praxis · doi:10.1024/1661-8157/a003153 · Cited by 1
A qualitative study of the preparedness of practitioners to care for people with motor neurone disease in their homes
Brewah, H. (2019) · Primary Health Care · doi:10.7748/phc.2019.e1515 · Cited by 1
Dissection and Immunohistochemistry of the Drosophila Adult Leg to Detect Changes at the Neuromuscular Junction for an Identified Motor Neuron
Stilwell, G., & Agudelo, A. (2022) · Journal of Visualized Experiments · doi:10.3791/62844-v · Cited by 1
Motor Neurone Disease
Nagaratnam, N., Nagaratnam, K., & Cheuk, G. (2018) · Springer eBooks · doi:10.1007/978-3-319-33434-9_37 · Cited by 1
Motor Neuron Disease: To Identify the Mimics and Chameleons at the Early Stage
Ekladious, A., & Jiang, B. (2022) · International Journal of Biomedical Research & Practice · doi:10.33425/2769-6294.1017 · Cited by 1
Case Report: Comprehensive management of Bulbar Motor Neuron disease in an elderly male: A Multidisciplinary case report approaching the treatment
Hullumani, S., V, & Mudey, R. P. (2024) · F1000Research · doi:10.12688/f1000research.144134.1 · Cited by 1
Rare Clinical Image of Kennedy’s Syndrome
Mudey, R. P., & Hullumani, S. (2024) · Neurology India · doi:10.4103/neurol-india.neurol-india-d-24-00196 · Cited by 1
Overview and audit against Motor Neurone Disease (MND) Association guidelines of a MND consultant’s practice over the last 3 years at the [Hospital]
Worku, D. A., Krishna, U., & Morrison, K. E. (2017) · Res Medica · doi:10.2218/resmedica.v24i1.1563 · Cited by 1
Neuroregenerative Rehabilitation Therapy with long-term Lithium in a Male Amyotrophic Lateral Sclerosis Patient: A Case Report.
Sharma, A. K., Sane, H. M., Pradhan, R., Paranjape, A., Gokulchandran, N., Kaur, J., Das, R., & Badhe, P. B. (2019) · International Journal Of Medical Science And Clinical Invention · doi:10.18535/ijmsci/v6i2.11 · Cited by 1
Stem Cell Therapy in Motor Neuron Disease
Sharma, A. K., Sane, H. M., Gokulchandran, N., Badhe, P. B., Paranjape, A., Pradhan, R., Das, R., & Biju, H. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.87116 · Cited by 1
A case study on Motor Neuron Disease
Ebin, T., Moos, P. V., & Nambi, A. (2021) · Journal of Ayurvedic and Herbal Medicine · doi:10.31254/jahm.2021.7104 · Cited by 1
Clinical Topics in Old Age Psychiatry
Lilford, P., Adshead, G., & Hughes, J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714 · Cited by 1
What Can Person-Centred Care in Dementia Learn from the Recovery Movement?
Hill, L., Roberts, G. A., & Perkins, R. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.018 · Cited by 1
Cognitive impairment in patients with amyotrophic lateral sclerosis: a neuropsychological perspective
Štukovnik, V., Zidar, J., & Repovš, G. (2013) · DOAJ (DOAJ: Directory of Open Access Journals)
Motor neurone disease - caring for the patient in general practice.
Zoing, M. C., & Kiernan, M. C. (2011) · PubMed
Palliative Nursing Care in other Neurological Conditions
Thomson, A., Ferguson, C., Warner, R., Kernohan, G. W., Hasson, F., & Hardyway, D. (2009) · doi:10.1002/9781444322705.ch11
The effect of mechanical ventilation on quality of life in patients with motor neurone disease
Smith, S. L., & McLeod, A. (2015) · British Journal of Neuroscience Nursing · doi:10.12968/bjnn.2015.11.5.220
Being differently the same: an exploration of the mediation of identity tensions in the sharing of illness experiences
Mazanderani, F., Locock, L., & powell, J. A. (2012)
Get the facts right: time for evidence-based ethics
MacKintosh, D. (2015) · Journal of Medical Ethics · doi:10.1136/medethics-2015-103052
Assessing residual neck mobility when wearing a cervical orthosis : an application in patients with motor neurone disease
Pancani, S. (2016) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)
Motor Neurone Disease
Nagaratnam, N., Nagaratnam, K., & Cheuk, G. (2017) · Springer eBooks · doi:10.1007/978-3-319-32700-6_37-1
Improving Motor Imagery Based Brain Computer Interfaces Using A Novel Physical Feedback TechniquePreprint
Haroun, M., & Salah, M. (2018) · arXiv (Cornell University) · doi:10.48550/arxiv.1805.08658
“This Condition isn't Going to get any Better so I can't see why we're Prolonging it”: Risks and Benefits of using Empirical Research to Inform Normative Decisions Concerning End-of-Life Care
Fistein, E., Clarke, G., Holland, A. J., & Barclay, S. I. G. (2018) · Journal of Disability & Religion · doi:10.1080/23312521.2018.1493959
Mental Health Laws from All UK Jurisdictions
Burrell, C., & Emmett, C. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.024
Motor neurone disease
Knight, L. E. (2020) · InnovAiT Education and inspiration for general practice · doi:10.1177/1755738020958024
Epidemiology and Mental Health in Old Age
Lilford, P., & Hughes, J. C. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.004
Mental Health in Parkinson’s Disease
Jones, S., Torsney, K., Scourfield, L., Berryman, K., & Henderson, E. J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.011
Mini-Mental State Examination for the Detection and Prediction of Dementia in People with and without Mild Cognitive Impairment
Mitchell, A. J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.014
Residence Capacity
Hughes, J. C., Poole, M., Louw, S., Greener, H., & Emmett, C. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.026
Concluding Reflections
Lilford, P. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.028
Vascular Dementia
Series, H. G., & Esiri, M. M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.005
Introductory Comments
Hughes, J. C. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.003
Supporting Self-Management in Early Dementia
Cheffey, J., Hill, L., & Roberts, G. A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.017
Deprivation of Liberty
Brindle, N., & Walsh, C. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.025
Controlling the Confusion
Colgate, R., Turner, A., & Rafferty, D. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.023
The Home Assessment in Old Age Psychiatry
Ng, B., & Atkins, M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.012
Young-Onset Dementias
Jefferies, K., & Agrawal, N. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.006
Mania in Late Life
Richards, F., & Curtice, M. J. R. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.008
Palliative Care in Dementia
Hughes, J. C., Jolley, D. J., Jordan, A., & Sampson, E. L. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.020
Alcohol Misuse in Older People
Rao, R., & CROME, I. B. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.009 · Cited by 1
Drug Misuse in Older People
Wagle, A., & Badrakalimuthu, V. R. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.010
Reducing the Healthcare Burden of Delirium
Meagher, D. J., O'Connell, H. P., Cullen, W., & Adamis, D. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.022
Rare and Unusual Dementias
Gupta, S., Fiertag, O., Thanulingam, T., Strange, B. A., & Warner, J. P. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.007
Driving in Dementia
Wilson, S., & Pinner, G. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.013
Preface
Hughes, J. C., & Lilford, P. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.001
Biomarkers and the Diagnosis of Preclinical Alzheimer’s Disease
Lilford, P., & Hughes, J. C. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.015
Understanding the Person with Dementia
Hughes, J. C., & Beatty, A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.027
Editors’ Note
Hughes, J. C., & Lilford, P. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.002
To Scan or Not to Scan
Sullivan, V., Majumdar, B., Richman, A. V., & Vinjamuri, S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108594714.016
Dissection and Immunohistochemistry of the Drosophila Adult Leg to Detect Changes at the Neuromuscular Junction for an Identified Motor Neuron
Stilwell, G., & Agudelo, A. (2022) · Journal of Visualized Experiments · doi:10.3791/62844
Recent Literature
Rousseau, P. C. (2008) · Journal of Palliative Medicine · doi:10.1089/jpm.2008.9876
Theme 7 Quality of Life and Palliative Care
(2015) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2015.1098812

Authors: McDermott, C. J., & Shaw, P. J.
Affiliations: University of Sheffield (GB)
Corresponding author: McDermott, Christopher J
ORCID: McDermott, Christopher J
Shaw, Pamela J
Venue: BMJ
Publisher: BMJ
Published: 2008-03-20
Volume: 336
Issue: 7645
Pages: 658-662
ISSN: 1756-1833 (ISSN-L)
0959-8138
DOI: 10.1136/bmj.39493.511759.be
PMC: PMC2270983
OpenAlex: W1993915028
Cited by: 220
References: 28
Citations by year: 2026: 8 · 2025: 12 · 2024: 12 · 2023: 11 · 2022: 14 · 2021: 11 · 2020: 35 · 2019: 14 · 2018: 8 · 2017: 15 · 2016: 11 · 2015: 16 · 2014: 9 · 2013: 12 · 2012: 9
FWCI: 4.92
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.bmj.org/licenses/tdm/1.0/terms-and-conditions.html (tdm)
Locations: BMJ (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
HighWire Press Open Archive (submittedVersion)
Topics: Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
Health Sciences › Medicine › Genetics (clinical) › Neurogenetic and Muscular Disorders Research
Health Sciences › Medicine › Clinical Neurology › Peripheral Neuropathies and Disorders
Keywords: motor neuron disease, diagnosis, management, primary care, symptom management, disease mechanisms, progressive paralysis, patient reassurance
MeSH terms: Antioxidants, Diagnosis, Differential, Humans, Physician-Patient Relations, Respiratory Therapy, Motor Neuron Disease, Neuroprotective Agents, Riluzole

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Diagnosis and management of motor neurone disease

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks