Measuring reliable change in cognition using the Edinburgh Cognitive and Behavioural ALS Screen (ECAS)-Reference-Cited by-同舟云学术

Measuring reliable change in cognition using the Edinburgh Cognitive and Behavioural ALS Screen (ECAS)

Published:2017-12-07 Issue:1-2 Volume:19 Page:65-73
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Crockford Christopher¹²^ORCID,Newton Judith¹³,Lonergan Katie⁴⁵,Madden Caoifa⁴⁵,Mays Iain⁴⁵,O’Sullivan Meabhdh⁴,Costello Emmet⁴⁵,Pinto-Grau Marta⁴⁵,Vajda Alice⁴,Heverin Mark⁴,Pender Niall⁵,Al-Chalabi Ammar⁶^ORCID,Hardiman Orla⁴⁷^ORCID,Abrahams Sharon¹²³

Affiliation:

1. Department of Psychology, Human Cognitive Neuroscience, University of Edinburgh, Edinburgh, UK,

2. Euan MacDonald Centre for Motor Neurone Disease Research, Royal Infirmary of Edinburgh, Edinburgh, UK,

3. Anne Rowling Regenerative Neurology Clinic, Royal Infirmary of Edinburgh, Edinburgh, UK,

4. Academic Unit of Neurology, Trinity College Dublin, Dublin, Ireland,

5. Department of Psychology, Beaumont Hospital, Dublin, Ireland,

6. Department of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, King’s College London, London, UK, and

7. Department of Neurology, Beaumont Hospital, Dublin, Ireland

Funder

Amyotrophic Lateral Sclerosis Association

Euan MacDonald Centre for Motor Neurone Disease Research, Health Research Board

Science Foundation Ireland

JPND

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

Link

https://tandfonline.com/doi/pdf/10.1080/21678421.2017.1407794

Reference27 articles.

1. Verbal fluency and executive dysfunction in amyotrophic lateral sclerosis (ALS)

2. Changes in cognition and behaviour in amyotrophic lateral sclerosis: nature of impairment and implications for assessment

3. Is language impairment more common than executive dysfunction in amyotrophic lateral sclerosis?

4. Neuropsychiatric changes precede classic motor symptoms in ALS and do not affect survival

5. Apathy is associated with poor prognosis in amyotrophic lateral sclerosis

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