Cargando…
Non-convulsive status epilepticus associated with neuronal intranuclear inclusion disease: A case report and literature review
We report a case of neuronal intranuclear inclusion disease (NIID) confirmed by detection of intranuclear inclusions in a skin biopsy specimen. Brain magnetic resonance imaging showed mild cerebral atrophy and linear hyperintensities at the corticomedullary junction on diffusion-weighted images. Thi...
Autores principales: | Shindo, Kazumasa, Tsuchiya, Mai, Hata, Takanori, Ichinose, Yuta, Koh, Kishin, Sone, Jun, Nagasaka, Takamura, Sobue, Gen, Takiyama, Yoshihisa |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403408/ https://www.ncbi.nlm.nih.gov/pubmed/30891404 http://dx.doi.org/10.1016/j.ebcr.2019.01.007 |
Ejemplares similares
-
Pathological findings in a patient with non-dystrophic myotonia with a mutation of the SCN4A gene; a case report
por: Hata, Takanori, et al.
Publicado: (2019) -
Age‐related changes in blood pressure and heart rates of patients with Parkinson's disease
por: Shindo, Kazumasa, et al.
Publicado: (2020) -
Neuronal Intranuclear Inclusion Disease Presenting with Resting Tremor
por: Kitagawa, Naoyuki, et al.
Publicado: (2014) -
Opsoclonus-myoclonus syndrome associated with multiple system atrophy
por: Shindo, Kazumasa, et al.
Publicado: (2014) -
Spinocerebellar ataxia type 31 associated with REM sleep behavior disorder: a case report
por: Shindo, Kazumasa, et al.
Publicado: (2019)