Takuya Miyabayashi

Japan

Last Updated: 09/26/2026

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Found 19 publications

The Clinical Course and Treatment of a Case of Refractory Systemic Juvenile Myasthenia Gravis Successfully Treated with Thymectomy.

The Clinical Course and Treatment of a Case of Refractory Systemic Juvenile Myasthenia Gravis Successfully Treated with Thymectomy.

Journal: The Tohoku journal of experimental medicine
Published: November 15, 2023

Multiple Cerebral Hemorrhages and White Matter Lesions Developing after Severe hMPV Pneumonia in a Patient with Trisomy 13: A Case Report and Review of the Literature.

Multiple Cerebral Hemorrhages and White Matter Lesions Developing after Severe hMPV Pneumonia in a Patient with Trisomy 13: A Case Report and Review of the Literature.

Journal: The Tohoku journal of experimental medicine
Published: July 06, 2022

Water intoxication: A clue to the presence of classical Fabry disease.

Water intoxication: A clue to the presence of classical Fabry disease.

Journal: Brain & development
Published: January 27, 2022

A first case of childhood chronic inflammatory demyelinating polyneuropathy associated with alopecia universalis.

A first case of childhood chronic inflammatory demyelinating polyneuropathy associated with alopecia universalis.

Journal: Brain & development
Published: January 24, 2022

Reduced efficacy of perampanel in patients with severe motor and intellectual disabilities syndrome and drug-resistant epilepsy: A single-center analysis from Japan.

Reduced efficacy of perampanel in patients with severe motor and intellectual disabilities syndrome and drug-resistant epilepsy: A single-center analysis from Japan.

Journal: Epilepsy research
Published: July 12, 2021

Fifteen-year follow-up of a patient with a DHDDS variant with non-progressive early onset myoclonic tremor and rare generalized epilepsy.

Fifteen-year follow-up of a patient with a DHDDS variant with non-progressive early onset myoclonic tremor and rare generalized epilepsy.

Journal: Brain & development
Published: May 15, 2020

Two cases of persistent falcine and occipital sinuses.

Two cases of persistent falcine and occipital sinuses.

Journal: Brain & development
Published: April 13, 2020

Two males with sick sinus syndrome in a family with 0.6 kb deletions involving major domains in MECP2.

Two males with sick sinus syndrome in a family with 0.6 kb deletions involving major domains in MECP2.

Journal: European journal of medical genetics
Published: March 16, 2019

Phenotype-genotype correlations in patients with GNB1 gene variants, including the first three reported Japanese patients to exhibit spastic diplegia, dyskinetic quadriplegia, and infantile spasms.

Phenotype-genotype correlations in patients with GNB1 gene variants, including the first three reported Japanese patients to exhibit spastic diplegia, dyskinetic quadriplegia, and infantile spasms.

Journal: Brain & development
Published: January 28, 2019

Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndrome.

Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndrome.

Journal: Journal of human genetics
Published: October 10, 2018

A novel homozygous mutation of the TFG gene in a patient with early onset spastic paraplegia and later onset sensorimotor polyneuropathy.

A novel homozygous mutation of the TFG gene in a patient with early onset spastic paraplegia and later onset sensorimotor polyneuropathy.

Journal: Journal of human genetics
Published: May 12, 2018

[18F]fluorodeoxyglucose-positron emission tomography study of genetically confirmed patients with Dravet syndrome.

[18F]fluorodeoxyglucose-positron emission tomography study of genetically confirmed patients with Dravet syndrome.

Journal: Epilepsy research
Published: April 25, 2018
Showing 1-12 of 19

Last Updated: 09/26/2026