Shota Shibata
Hongo, 1138655, Japan
Last Updated: 09/26/2026
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Found 10 publications
Genotype-phenotype correlations in neuronal intranuclear inclusion disease-related retinopathy with CGG repeat increases in NOTCH2NLC.
Journal: Journal of neurology
Published: November 03, 2025
Proteomic profile of nuclei containing p62-positive inclusions in a patient with neuronal intranuclear inclusion disease.
Journal: Neurobiology of disease
Published: August 02, 2022
CSF P-Tau181 and Other Biomarkers in Patients With Neuronal Intranuclear Inclusion Disease.
Journal: Neurology
Published: June 16, 2022
Correction to: Efficacy of canakinumab on AA amyloidosis in late-onset NLRP3-associated autoinflammatory disease with an I574F somatic mosaic mutation.
Journal: Clinical rheumatology
Published: April 01, 2022
Efficacy of canakinumab on AA amyloidosis in late-onset NLRP3-associated autoinflammatory disease with an I574F somatic mosaic mutation.
Journal: Clinical rheumatology
Published: February 25, 2022
Expanded clinical spectrum of oculopharyngodistal myopathy type 1.
Journal: Muscle & nerve
Published: December 09, 2021
Clinical Characteristics of Neuronal Intranuclear Inclusion Disease-Related Retinopathy With CGG Repeat Expansions in the NOTCH2NLC Gene.
Journal: Investigative ophthalmology & visual science
Published: September 15, 2020
Adult-onset neuronal intranuclear inclusion disease mimicking Fragile X-associated tremor-ataxia syndrome in ethnic Chinese patients.
Journal: Parkinsonism & related disorders
Published: January 15, 2020
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease.
Journal: Nature genetics
Published: August 30, 2018
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.
Journal: Nature genetics
Published: March 27, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026