- Abstract:
-
There is no test for amyotrophic lateral sclerosis (ALS) and so attempts have been made to produce standardised diagnostic criteria based on clinical and electrophysiological findings. The phenotypic classification of the subtypes of ALS is also based on clinical features, which leads to conflation of diagnosis and phenotype. We gave a five question online survey to ALS specialists to explore the range of descriptors and their use. Of 101 specialists approached, 72 completed the survey. The m...
Expand abstract - Publication status:
- Published
- Peer review status:
- Peer reviewed
- Version:
- Accepted Manuscript
- Files:
-
-
(pdf, 105.1KB)
-
- Publisher copy:
- 10.1080/21678421.2016.1181766
-
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- Grant:
- EU Joint Programme - Neurodegenerative Disease Research
- Grant:
- EU Joint Programme - Neurodegenerative Disease Research
- Publisher:
- Taylor and Francis Publisher's website
- Journal:
- Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Journal website
- Volume:
- 17
- Issue:
- 7-8
- Pages:
- 600-604
- Publication date:
- 2016-05-18
- DOI:
- EISSN:
-
2167-9223
- ISSN:
-
2167-8421
- URN:
-
uuid:b88752fa-3110-4078-88df-4bccd26988fd
- Source identifiers:
-
619025
- Local pid:
- pubs:619025
- Paper number:
- 7-8
- Copyright holder:
- World Federation of Neurology on behalf of the Research Group on Motor Neuron Diseases
- Copyright date:
- 2016
- Notes:
-
Copyright © 2016 World Federation of Neurology on behalf of the Research Group on Motor Neuron Diseases. This is the accepted manuscript version of the article. The final version is available online from Taylor and Francis at: https://doi.org/10.1080/21678421.2016.1181766
Journal article
Analysis of terms used for the diagnosis and classification of amyotrophic lateral sclerosis and motor neuron disease
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