Article ID Journal Published Year Pages File Type
8275317 Journal of the Neurological Sciences 2015 7 Pages PDF
Abstract
The majority of TDLs evolve into MS or NMOSD. However, despite extensive diagnostic work-ups and long-term follow-ups, the etiology of TDLs was unknown for some patients.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
Authors
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