Longitudinal changes of outcome measures in spinal and bulbar muscular atrophy
Brain, 07/17/2012
Hashizume A et al. – The results suggest that patients with spinal and bulbar muscular atrophy show a slow but steady progression of motor dysfunction over time that is independent of CAG repeat length or clinical phenotype, and that objective outcome measures may be used to evaluate disease severity at an early stage of this disease.



