Jun Takei

Kagoshima, 8908520, Japan

Last Updated: 09/26/2026

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Found 12 publications

Brain biopsy and metagenomic sequencing enhance aetiological diagnosis of encephalitis.

Brain biopsy and metagenomic sequencing enhance aetiological diagnosis of encephalitis.

Journal: Brain communications

Published: September 24, 2024

Linking LRP12 CGG repeat expansion to inherited peripheral neuropathy.

Linking LRP12 CGG repeat expansion to inherited peripheral neuropathy.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: January 17, 2024

A case of myofibrillary myopathy due to Bcl2-Associated Athanogene 3 (BAG3) mutation complicated by peripheral neuropathy

A case of myofibrillary myopathy due to Bcl2-Associated Athanogene 3 (BAG3) mutation complicated by peripheral neuropathy

Journal: Rinsho shinkeigaku = Clinical neurology

Published: November 21, 2023

Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan.

Clinical variability associated with intronic FGF14 GAA repeat expansion in Japan.

Journal: Annals of clinical and translational neurology

Published: August 09, 2023

Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation.

Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation.

Journal: Frontiers in neurology

Published: June 17, 2023

Clinical phenotypic diversity of NOTCH2NLC-related disease in the largest case series of inherited peripheral neuropathy in Japan.

Clinical phenotypic diversity of NOTCH2NLC-related disease in the largest case series of inherited peripheral neuropathy in Japan.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: November 15, 2022

Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible.

Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible.

Journal: Biomedicines

Published: June 07, 2022

Genetic and clinical features of cerebellar ataxia with RFC1 biallelic repeat expansions in Japan.

Genetic and clinical features of cerebellar ataxia with RFC1 biallelic repeat expansions in Japan.

Journal: Frontiers in neurology

Published: May 25, 2022

Novel heterozygous variants of SLC12A6 in Japanese families with Charcot-Marie-Tooth disease.

Novel heterozygous variants of SLC12A6 in Japanese families with Charcot-Marie-Tooth disease.

Journal: Annals of clinical and translational neurology

Published: March 21, 2022

Novel de novo POLR3B mutations responsible for demyelinating Charcot-Marie-Tooth disease in Japan.

Novel de novo POLR3B mutations responsible for demyelinating Charcot-Marie-Tooth disease in Japan.

Journal: Annals of clinical and translational neurology

Published: December 16, 2021

An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families.

An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families.

Journal: Journal of human genetics

Published: November 10, 2021

Efficacy of potassium bromide in the treatment of drug-resistant epilepsy: a case of new-onset refractory status epilepticus.

Efficacy of potassium bromide in the treatment of drug-resistant epilepsy: a case of new-onset refractory status epilepticus.

Journal: Rinsho shinkeigaku = Clinical neurology

Published: October 25, 2016

Showing 1-12 of 12

Last Updated: 09/26/2026