Aiko Nishikawa

Shinjuku, 1628666, Japan

Last Updated: 09/26/2026

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Found 10 publications

COVID-19 infection and vaccination in children with Dravet syndrome or infantile epileptic spasms syndrome: An internet survey in Japan.

COVID-19 infection and vaccination in children with Dravet syndrome or infantile epileptic spasms syndrome: An internet survey in Japan.

Journal: Brain & development

Published: November 27, 2024

Ictal vocalizations are relatively common in myoclonic-atonic seizures associated with Doose syndrome: an audio-video-polygraphic analysis.

Ictal vocalizations are relatively common in myoclonic-atonic seizures associated with Doose syndrome: an audio-video-polygraphic analysis.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: September 14, 2021

Transition from pediatric to adult care in a Japanese cohort of childhood-onset epilepsy: prevalence of epileptic syndromes and complexity in the transition.

Transition from pediatric to adult care in a Japanese cohort of childhood-onset epilepsy: prevalence of epileptic syndromes and complexity in the transition.

Journal: Seizure

Published: January 28, 2021

Morphometric analysis of spike-wave complexes (SWCs) causing myoclonic seizures in children with idiopathic myoclonic epilepsies - A positive SWC component correlates with myoclonic intensity.

Morphometric analysis of spike-wave complexes (SWCs) causing myoclonic seizures in children with idiopathic myoclonic epilepsies - A positive SWC component correlates with myoclonic intensity.

Journal: Brain & development

Published: January 28, 2021

Low-dose phenobarbital for epilepsy with myoclonic absences: A case report.

Low-dose phenobarbital for epilepsy with myoclonic absences: A case report.

Journal: Brain & development

Published: November 09, 2020

Unexpected elevation in valproic acid concentration and agranulocytosis in a patient with short-chain acyl-CoA dehydrogenase deficiency.

Unexpected elevation in valproic acid concentration and agranulocytosis in a patient with short-chain acyl-CoA dehydrogenase deficiency.

Journal: Brain & development

Published: October 17, 2020

A de novo GABRB2 variant associated with myoclonic status epilepticus and rhythmic high-amplitude delta with superimposed (poly) spikes (RHADS).

A de novo GABRB2 variant associated with myoclonic status epilepticus and rhythmic high-amplitude delta with superimposed (poly) spikes (RHADS).

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: August 08, 2020

A missense variant of SMC1A causes periodic pharmaco-resistant cluster seizures similar to PCDH19-related epilepsy.

A missense variant of SMC1A causes periodic pharmaco-resistant cluster seizures similar to PCDH19-related epilepsy.

Journal: Epilepsy research

Published: April 27, 2019

An episode of acute encephalopathy with biphasic seizures and late reduced diffusion followed by hemiplegia and intractable epilepsy observed in a patient with a novel frameshift mutation in HNRNPU.

An episode of acute encephalopathy with biphasic seizures and late reduced diffusion followed by hemiplegia and intractable epilepsy observed in a patient with a novel frameshift mutation in HNRNPU.

Journal: Brain & development

Published: February 20, 2018

Ketogenic diet therapy can improve ACTH-resistant West syndrome in Japan.

Ketogenic diet therapy can improve ACTH-resistant West syndrome in Japan.

Journal: Brain & development

Published: September 30, 2013

Showing 1-10 of 10

Last Updated: 09/26/2026