Case report: 10-year follow-up of a patient with neuronal intranuclear inclusion disease and a literature review
Neuronal intranuclear inclusion disease (NIID) is a rare, progressive neurodegenerative disease with variable clinical manifestations. High signals on diffusion-weighted imaging (DWI) along the corticomedullary junction (CMJ) are a specific feature of NIID. Only a few reports have observed patients...
Saved in:
| Main Authors: | Kenji Yoshida, Tomotsugu Kaga, Sachiko Hosoyama, Jun-ichi Niwa, Jun Sone, Naoki Mabuchi |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2025-01-01
|
| Series: | Frontiers in Neuroscience |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fnins.2024.1530160/full |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A case report of neuronal intranuclear inclusion disease and literature review
by: Jie Li, et al.
Published: (2024-12-01) -
A case of neuronal intranuclear inclusion disease (NIID) presenting with hydrocephalus-like clinical features: case report
by: Yonghong Wang, et al.
Published: (2025-02-01) -
Dual diagnosis at the neuro-immune interface: a case report of neuronal intranuclear inclusion disease with acute anti-CASPR2 encephalitis
by: Wan Zhu, et al.
Published: (2025-08-01) -
Editorial: The contribution of autophagy to neuronal metabolism
by: Francois Singh, et al.
Published: (2025-04-01) -
Neuron-Glial2 (NG2) cells: A promising target for neuroinflammation-related neurodegeneration
by: Zaw Myo Hein, et al.
Published: (2025-06-01)