Yuri Sakaguchi

Matsumoto, 3908621, Japan

Last Updated: 09/26/2026

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Found 18 publications

Refining risk stratification and understanding epilepsy severity in adults with profound intellectual and multiple disabilities: Author reply to commentary.

Refining risk stratification and understanding epilepsy severity in adults with profound intellectual and multiple disabilities: Author reply to commentary.

Journal: Epilepsy research

Published: June 06, 2026

Risk factors of epilepsy severity in institutionalized adults with profound intellectual and multiple disabilities from childhood.

Risk factors of epilepsy severity in institutionalized adults with profound intellectual and multiple disabilities from childhood.

Journal: Epilepsy research

Published: November 09, 2025

Early-phase EEG power spectrum analysis may differentiate acute encephalopathy with biphasic seizures and late reduced diffusion from prolonged febrile seizures.

Early-phase EEG power spectrum analysis may differentiate acute encephalopathy with biphasic seizures and late reduced diffusion from prolonged febrile seizures.

Journal: Epilepsy research

Published: October 19, 2024

The Utility of Limited-Montage Electroencephalography for Seizure Detection in Children.

The Utility of Limited-Montage Electroencephalography for Seizure Detection in Children.

Journal: Pediatric neurology

Published: March 24, 2022

Rituximab treatment for a child with antibody-negative limbic encephalitis.

Rituximab treatment for a child with antibody-negative limbic encephalitis.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: March 23, 2022

Vanishing basal ganglia in ATP1A3-related polymicrogyria.

Vanishing basal ganglia in ATP1A3-related polymicrogyria.

Journal: American journal of medical genetics. Part A

Published: June 23, 2021

Refractory cerebral infarction in a child with an ACTA2 mutation.

Refractory cerebral infarction in a child with an ACTA2 mutation.

Journal: Brain & development

Published: October 11, 2020

Decisive evidence of direct effect of ACTH treatment in West syndrome: A case report.

Decisive evidence of direct effect of ACTH treatment in West syndrome: A case report.

Journal: Seizure

Published: September 06, 2020

Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis.

Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis.

Journal: American journal of medical genetics. Part A

Published: June 23, 2020

HPeV3-associated acute encephalitis/encephalopathy among Japanese infants.

HPeV3-associated acute encephalitis/encephalopathy among Japanese infants.

Journal: Brain & development

Published: June 09, 2020

Hereditary spastic paraplegia masqueraded by congenital melanocytic nevus syndrome: Dual pathogenesis of germline non-mosaicism and somatic mosaicism.

Hereditary spastic paraplegia masqueraded by congenital melanocytic nevus syndrome: Dual pathogenesis of germline non-mosaicism and somatic mosaicism.

Journal: European journal of medical genetics

Published: September 07, 2019

CNOT2 as the critical gene for phenotypes of 12q15 microdeletion syndrome.

CNOT2 as the critical gene for phenotypes of 12q15 microdeletion syndrome.

Journal: American journal of medical genetics. Part A

Published: September 12, 2018

Showing 1-12 of 18

Last Updated: 09/26/2026