[HTML][HTML] Clinical and mechanism advances of neuronal intranuclear inclusion disease
Y Liu, H Li, X Liu, B Wang, H Yang, B Wan… - Frontiers in Aging …, 2022 - frontiersin.org
Due to the high clinical heterogeneity of neuronal intranuclear inclusion disease (NIID), it is
easy to misdiagnose this condition and is considered to be a rare progressive …
easy to misdiagnose this condition and is considered to be a rare progressive …
Recent advances in CGG repeat diseases and a proposal of fragile X-associated tremor/ataxia syndrome, neuronal intranuclear inclusion disease, and …
H Ishiura, S Tsuji, T Toda - Journal of Human Genetics, 2023 - nature.com
While whole genome sequencing and long-read sequencing have become widely available,
more and more focuses are on noncoding expanded repeats. Indeed, more than half of …
more and more focuses are on noncoding expanded repeats. Indeed, more than half of …
[PDF][PDF] A case of neuronal intranuclear inclusion disease with recurrent vomiting and without apparent DWI abnormality for the first seven years
S Okamura, M Takahashi, K Abe, A Inaba, J Sone… - Heliyon, 2020 - cell.com
Neuronal intranuclear inclusion disease (NIID) is a rare, neurodegenerative disorder
characterized by the presence of eosinophilic hyaline intranuclear inclusions, which are …
characterized by the presence of eosinophilic hyaline intranuclear inclusions, which are …
Prevalence of fragile X-associated tremor/ataxia syndrome in patients with cerebellar ataxia in Japan
Y Higuchi, M Ando, A Yoshimura, S Hakotani, Y Koba… - The Cerebellum, 2021 - Springer
The presence of fragile X mental retardation 1 (FMR1) premutation has been linked to
patients with a certain type of cerebellar ataxia, the fragile X-associated tremor/ataxia …
patients with a certain type of cerebellar ataxia, the fragile X-associated tremor/ataxia …
Identifying patients with neuronal intranuclear inclusion disease in Singapore using characteristic diffusion-weighted MR images
Purpose Adult-onset neuronal intranuclear inclusion disease (NIID) is a rare
neurodegenerative disorder described mainly in the Japanese population, with …
neurodegenerative disorder described mainly in the Japanese population, with …
Coexistence of neuronal intranuclear inclusion disease and amyotrophic lateral sclerosis: an autopsy case
A Sugiyama, T Takeda, M Koide, H Yokota, H Mukai… - BMC neurology, 2021 - Springer
Background Neuronal intranuclear inclusion disease (NIID) is a rare neurodegenerative
disease. Pathologically, it is characterized by eosinophilic hyaline intranuclear inclusions in …
disease. Pathologically, it is characterized by eosinophilic hyaline intranuclear inclusions in …
A case report of sporadic adult neuronal intranuclear inclusion disease (NIID) with stroke-like onset
P Lin, H Jin, KC Yi, XS He, SF Lin, G Wu… - Frontiers in …, 2020 - frontiersin.org
Background: Neuronal intranuclear inclusion disease (NIID) is a rare neurodegenerative
disease. The clinical manifestations of NIID are complex and easily misdiagnosed. Based on …
disease. The clinical manifestations of NIID are complex and easily misdiagnosed. Based on …
NOTCH2NLC-linked neuronal intranuclear inclusion body disease and fragile X-associated tremor/ataxia syndrome
We read with interest two separate reports in Brain (Sone et al., 2016; Sun et al., 2020) on
neuronal intranuclear inclusion body disease (NIID), a neurodegenerative disease …
neuronal intranuclear inclusion body disease (NIID), a neurodegenerative disease …
Adult-onset neuronal intranuclear inclusion disease, with both stroke-like onset and encephalitic attacks: a case report
Y Huang, G Jin, Q Zhan, Y Tian, L Shen - BMC neurology, 2021 - Springer
Background Neuronal intranuclear inclusion disease (NIID) is a neurodegenerative disease,
the clinical manifestations of which are complex and easily misdiagnosed. NIID clinical …
the clinical manifestations of which are complex and easily misdiagnosed. NIID clinical …
Advances on the Mechanisms and Therapeutic Strategies in Non-coding CGG Repeat Expansion Diseases
Y Zhang, X Liu, Z Li, H Li, Z Miao, X Xu - Molecular Neurobiology, 2024 - Springer
Non-coding CGG repeat expansions within the 5′ untranslated region are implicated in a
range of neurological disorders, including fragile X-associated tremor/ataxia syndrome …
range of neurological disorders, including fragile X-associated tremor/ataxia syndrome …