Chisato Tamai
Okazaki, Japan
Last Updated: 09/26/2026
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Found 8 publications
A case of neuronal intranuclear inclusion disease presenting with leukoencephalopathy after the diagnosis of Charcot-Marie-Tooth disease type 4C
Journal: Rinsho shinkeigaku = Clinical neurology
Published: December 14, 2025
A case of neuronal intranuclear inclusion disease with coexisting Alzheimer's disease biomarker signature in cerebrospinal fluid
Journal: Rinsho shinkeigaku = Clinical neurology
Published: November 24, 2025
Clinical and imaging characteristics of NOTCH3-negative CADASIL-suspected patients with NOTCH2NLC GGC repeat expansions.
Journal: Journal of human genetics
Published: November 02, 2025
Asthma-like bronchodilator responsiveness in patients with neuronal intranuclear inclusion disease.
Journal: Scientific reports
Published: September 02, 2025
A case of fragile X-associated tremor/ataxia syndrome with superior cerebellar peduncle lesions.
Journal: eNeurologicalSci
Published: July 05, 2024
Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation.
Journal: Brain pathology (Zurich, Switzerland)
Published: March 26, 2023
NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment.
Journal: Acta neuropathologica communications
Published: February 19, 2023
First detailed case report of a pediatric patient with neuronal intranuclear inclusion disease diagnosed by NOTCH2NLC genetic testing.
Journal: Brain & development
Published: February 01, 2022
Showing 1-8 of 8
Last Updated: 09/26/2026