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dc.contributor.authorGnanapavan, Sen_US
dc.contributor.authorGiovannoni, Gen_US
dc.date.accessioned2015-01-05T17:26:54Z
dc.date.issued2015en_US
dc.identifier.issn1866-3370en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/6325
dc.description.abstractExisting clinical outcomes of disease activity, including relapse rates, are inherently insensitive to the underlying pathological process in MS. Moreover, it is extremely difficult to measure clinical disability in patients, which is often a retrospective assessment, and definitely not within the time frame of a clinical trial. Biomarkers , conversely are more specific for a pathologic process and if used correctly can prove invaluable in the diagnosis, stratification and monitoring of disease activity, including any subclinical activity which is not visible to the naked eye. In this chapter, we discuss the development of neurofilaments as surrogate outcomes of disability in MS. The validation and qualification are vital steps in biomarker development and to gaining acceptance in scientific community, and the pitfalls leading up to this are also discussed.en_US
dc.format.extent179 - 194en_US
dc.languageengen_US
dc.relation.ispartofCurr Top Behav Neuroscien_US
dc.subjectBiobanken_US
dc.subjectBiomarkeren_US
dc.subjectNetworksen_US
dc.subjectNeurofilamentsen_US
dc.subjectQualificationen_US
dc.subjectValidationen_US
dc.subjectBiomarkersen_US
dc.subjectDisease Progressionen_US
dc.subjectHumansen_US
dc.subjectMultiple Sclerosisen_US
dc.subjectNeurofilament Proteinsen_US
dc.titleDeveloping Biomarkers for MS.en_US
dc.typeArticle
dc.rights.holder© Springer International Publishing Switzerland 2014
dc.identifier.doi10.1007/7854_2014_362en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/25502545en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume26en_US


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