Found: 3
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Adult-onset metachromatic leukodystrophy with compound heterozygous ARSA gene mutation presented with mania and cognitive decline.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
A case of early-onset familial Alzheimer’s disease with both APP and novel PSEN2 mutations presenting with non-amnestic features.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A case of TREM2 mutation presenting with features of progressive non-fluent aphasia and without bone involvement.
- Published in:
- 2017
- By:
- Publication type:
- Case Study