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Journal article

Biomarkers in amyotrophic lateral sclerosis: opportunities and limitations.

Abstract:
Insights into the mechanisms of amyotrophic lateral sclerosis (ALS) have relied predominantly on the study of postmortem tissue. Modern technology has improved the ability of scientists to probe effectively the underlying biology of ALS by examination of genomic, proteomic and physiological changes in patients, as well as to monitor functional and structural changes in patients over the course of disease. While effective treatments for ALS are lacking, the discovery of biomarkers for this disease offers clinicians tools for rapid diagnosis, improved ways to monitor disease progression, and insights into the pathophysiology of sporadic ALS. The ultimate aim is to broaden the therapeutic options for patients with this disease.
Publication status:
Published

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Publisher copy:
10.1038/nrneurol.2011.151

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author


Journal:
Nature reviews. Neurology More from this journal
Volume:
7
Issue:
11
Pages:
631-638
Publication date:
2011-11-01
DOI:
EISSN:
1759-4766
ISSN:
1759-4758


Language:
English
Keywords:
Pubs id:
pubs:245053
UUID:
uuid:183e6a4d-dabb-4da8-881a-3aaedbd259f4
Local pid:
pubs:245053
Source identifiers:
245053
Deposit date:
2013-11-16
ARK identifier:

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