Abstract
Multiple sclerosis (MS) is the commonest cause of acquired neurological disability in young adults. It is a multi-focal and multi-phasic immune-mediated disorder characterised pathologically by inflammatory demyelination, axonal injury and partial remyelination (Compston and Coles 2008). Treatments for MS thus have two aims: to prevent and to repair damage that has already occurred. Although important advances in treatment to reduce relapse rate have been made in the last two decades, more limited progress has been achieved in terms of definitive treatments for relapses and the slowing, cessation or reversal of disease progression (see Chap. 10). The lack of such therapies represents a substantial gap in the treatment of MS.
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Connick, P., Kolappan, M., Compston, A., Chandran, S. (2013). Designing Clinical Trials to Test Neuroprotective Therapies in Multiple Sclerosis. In: Duncan, I., Franklin, R. (eds) Myelin Repair and Neuroprotection in Multiple Sclerosis. Springer, Boston, MA. https://doi.org/10.1007/978-1-4614-2218-1_11
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