Munetsugu Hara

Kurume, Japan

Last Updated: 09/26/2026

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Found 15 publications

Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

Journal: Clinical genetics

Published: June 05, 2026

Sertraline treatment for paroxysmal nonkinesigenic dyskinesia comorbid with anxiety and depression.

Sertraline treatment for paroxysmal nonkinesigenic dyskinesia comorbid with anxiety and depression.

Journal: eNeurologicalSci

Published: August 06, 2023

Perampanel markedly improved clinical seizures in a patient with a Rett-like phenotype and 960-kb deletion on chromosome 9q34.11 including the STXBP1.

Perampanel markedly improved clinical seizures in a patient with a Rett-like phenotype and 960-kb deletion on chromosome 9q34.11 including the STXBP1.

Journal: Clinical case reports

Published: November 05, 2021

Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.

Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.

Journal: Nature communications

Published: November 26, 2018

Three Cases of KCNT1 Mutations: Malignant Migrating Partial Seizures in Infancy with Massive Systemic to Pulmonary Collateral Arteries.

Three Cases of KCNT1 Mutations: Malignant Migrating Partial Seizures in Infancy with Massive Systemic to Pulmonary Collateral Arteries.

Journal: The Journal of pediatrics

Published: April 24, 2017

De novo HDAC8 mutation causes Rett-related disorder with distinctive facial features and multiple congenital anomalies.

De novo HDAC8 mutation causes Rett-related disorder with distinctive facial features and multiple congenital anomalies.

Journal: Brain & development

Published: April 19, 2017

Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome.

Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome.

Journal: Scientific reports

Published: January 13, 2017

Ghrelin improves dystonia and tremor in patients with Rett syndrome: A pilot study.

Ghrelin improves dystonia and tremor in patients with Rett syndrome: A pilot study.

Journal: Journal of the neurological sciences

Published: November 29, 2016

De novo KCNT1 mutations in early-onset epileptic encephalopathy.

De novo KCNT1 mutations in early-onset epileptic encephalopathy.

Journal: Epilepsia

Published: June 08, 2015

Disturbance of cardiac gene expression and cardiomyocyte structure predisposes Mecp2-null mice to arrhythmias.

Disturbance of cardiac gene expression and cardiomyocyte structure predisposes Mecp2-null mice to arrhythmias.

Journal: Scientific reports

Published: November 19, 2014

Clinically mild encephalitis with a reversible splenial lesion (MERS) after mumps vaccination.

Clinically mild encephalitis with a reversible splenial lesion (MERS) after mumps vaccination.

Journal: Journal of the neurological sciences

Published: October 08, 2014

De novo SHANK3 mutation causes Rett syndrome-like phenotype in a female patient.

De novo SHANK3 mutation causes Rett syndrome-like phenotype in a female patient.

Journal: American journal of medical genetics. Part A

Published: December 12, 2013

Showing 1-12 of 15

Last Updated: 09/26/2026