Abstract
British Journal of Neuroscience NursingVol. 12, No. 1 BriefingCognition and motor neurone disease: the factsJackie HillJackie HillSearch for more papers by this authorJackie HillPublished Online:26 Feb 2016https://doi.org/10.12968/bjnn.2016.12.1.38AboutSectionsView articleView Full TextPDF/EPUB ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareShare onFacebookTwitterLinked InEmail View article References Abrahams S, Leigh PN, Goldstein LH (2005). Cognitive change in ALS: a prospective study. Neurology 64(7): 1222–26 Crossref, Google ScholarAbrahams S, Newton J, Niven E et al. (2014) Screening for cognition and behaviour changes in ALS. Amyotroph Lateral Scler Frontotemporal Degener 15(1–2): 9–14 Crossref, Google ScholarBäumer D, Talbot K, Turner MR (2014) Advances in motor neurone disease. J R Soc Med 107(1): 14–21 Crossref, Google ScholarChiò A, Ilardi A, Cammarosano S et al. (2012) Neurobehavioral dysfunction in ALS has a negative effect on outcome and use of PEG and NIV. Neurology 78(14): 108–9 Crossref, Google ScholarElamin M, Phukan J, Bede P et al. (2011) Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia. Neurology 76(14): 1263–9 Crossref, Google ScholarGibbons ZC, Richardson A, Neary D et al. (2008) Behaviour in amyotrophic lateral sclerosis. Amyotrop Lateral Scler 9(2): 67–74 Crossref, Google ScholarGirardi A, MacPherson SE, Abrahams S (2011) Deficits in emotional and social cognition in amyotrophic lateral sclerosis. Neuropsychology 25(1): 53–65 Crossref, Google ScholarGoldstein LH, Abrahams S (2013) Changes in cognition and behavioural in amyotrophic lateral sclerosis: nature of impairment and implications of assessment. Lancet Neurol 12(4): 368–80 Crossref, Google ScholarHogden A, Greenfield D, Nugus P et al. (2013) What are the roles of carers in decision-making for amyotrophic lateral sclerosis multidisciplinary care? Patient Prefer Adherence 7: 171–81 Crossref, Google ScholarLillo P, Hodges JR (2009) Frontotemporal dementia and motor neurone disease: overlapping clinic-pathological disorders. J Clin Neurosci 16(9): 113–5 Crossref, Google ScholarLillo P, Mioshi E, Hodges JR (2012) Caregiver burden in amyotrophic lateral sclerosis is more dependent on patients' behavioural changes than physical disability: a comparative study. BMC Neurol 12: 156 Crossref, Google ScholarLomen-Hoerth MD, Murphy J, Langmore S et al. (2003) Are amyotrophic lateral sclerosis patients cognitively normal? Neurology 60(7): 1094–7 Crossref, Google ScholarMerrilees J, Klapper J, Murphy J et al. (2010) Cognitive and behavioural challenges in caring for patients with frontotemporal dementia and amyotrophic lateral sclerosis. Amyotroph Lateral Scler 11(3): 298–302 Crossref, Google ScholarMioshi E, Bristow M, Cook R et al. (2009) Factors underlying caregiver stress in frontotemporal dementia and Alzheimer's disease. Dement Geriatr Cogn Disord 27(1): 76–81 Crossref, Google ScholarMioshi E, Caga J, Lillo P et al. (2014) Neuropsychiatric changes precede classic motor symptoms in ALS and do not affect survival. Neurology 82(2): 149–155 Crossref, Google ScholarMotor Neurone Disease (MND) Association (2015) For professionals. http://tinyurl.com/zq3ak8x (accessed 29 January 2016) Google ScholarMurphy JM, Henry RG, Langmore S (2007) Continuum of frontal lobe impairment in amyotrophic lateral sclerosis. Arch Neurol 64(4): 530–4 Crossref, Google ScholarNational Clinical Guideline Centre (2015) Motor neurone disease: assessment and management. http://tinyurl.com/j9uqqdq (accessed 29 January 2016) Google ScholarNewsom-Davis IC, Lyall RA, Leigh PN, Moxham J, Goldstein LH (2001). The effect of non-invasive positive pressure ventilation (NIPPV) on cognitive function in amyotrophic lateral sclerosis (ALS): a prospective study. J Neurol Neurosurg Psychiatry 71(4): 482–7 Crossref, Google ScholarPijnenburg Y (2011) New diagnostic criteria for the behavioral variant of frontotemporal dementia. Eur Neurol Rev 6(4): 234–7 Crossref, Google ScholarStrong MJ, Grace GM, Freedman M et al. (2009) Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis. Amyotroph Lateral Scer 10(3): 131–46 Crossref, Google ScholarZago S, Poletti B, Morelli C et al. (2011) Amyotrophic lateral sclerosis and frontotemporal dementia (ALS-FTD). Arch Ital Biol 149(1): 39–56 Google Scholar FiguresReferencesRelatedDetailsCited byCommunication and cognitive impairments and health care decision making in MND: A narrative review8 July 2019 | Journal of Evaluation in Clinical Practice, Vol. 25, No. 6The challenges of dysphagia in treating motor neurone diseaseSiobhan Vesey7 July 2017 | British Journal of Community Nursing, Vol. 22, No. Sup7 2 February 2016Volume 12Issue 1ISSN (print): 1747-0307ISSN (online): 2052-2800 Metrics History Published online 26 February 2016 Published in print 2 February 2016 Information© MA Healthcare LimitedPDF download
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