Familial neuronal intranuclear inclusion disease complicated by subcortical hemorrhage
An 80‐year‐old woman presented with loss of appetite. At age 78, she was diagnosed as familial neuronal intranuclear inclusion disease (NIID) based on (i) leukoencephalopathy with hyperintensities along the corticomedullary junction on diffusion‐weighted imaging (DWI) revealed by brain magnetic reso...
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Veröffentlicht in: | Neurology and clinical neuroscience 2019-05, Vol.7 (3), p.136-138 |
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Format: | Artikel |
Sprache: | eng |
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