ArticleFrontiers in neurology2022
Unraveling rare form of adult-onset NIID by characteristic brain MRI features: A single-center retrospective review.
Article in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 7 citations in OpenAlex.
- Distinctive hydrocephalus-like phenotype in NOTCH2NLC-related neuronal intranuclear inclusion disease: clinicopathological features and therapeutic implications.Acta neuropathologica communications · 2026Article
- Neuronal intranuclear inclusion disease caused by NOTCH2NLC gene expansion: a case report and literature review.BMC neurology · 2026Review
- Clinics in diagnostic imaging (224).Singapore medical journal · 2025Article
- A case of neuronal intranuclear inclusion disease (NIID) presenting with hydrocephalus-like clinical features: case report.BMC neurology · 2025Article
- Not your usual neurodegenerative disease: a case report of neuronal intranuclear inclusion disease with unconventional imaging patterns.Frontiers in neuroscience · 2023Article
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Authors and funding
9 authors at 2 institutions in 1 country.
Funding
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Abstract
Adult-onset neuronal intranuclear inclusion disease (NIID) is a rare neurodegenerative disorder with high clinical heterogeneity. Previous studies indicated that the high-intensity signals in the corticomedullary junction on diffusion-weighted imaging (DWI) on brain MRI, known as the "ribbon sign," could serve as a strong diagnostic clue. Here we used the explorative approach to study the undiagnosed rate of adult-onset NIID in a single center in China
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