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Treatment of benign focal epilepsies in children: When and how should be treated?

Brain & development (Tokyo. 1979), 2011-03, Vol.33 (3), p.207-212

Oguni, Hirokazu

2011

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

Brain & development (Tokyo. 1979), 2021-05, Vol.43 (5), p.666-668

2021

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CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate

Scientific reports, 2022-05, Vol.12 (1), p.6505-6505, Article 6505

2022

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

Brain & development (Tokyo. 1979), 2021-08, Vol.43 (7), p.775-782

2021

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Outcome of ketogenic diets in GLUT1 deficiency syndrome in Japan: A nationwide survey

Brain & development (Tokyo. 1979), 2016-08, Vol.38 (7), p.628-637

2016

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A reappraisal of interictal EEG characteristics in self-limited epilepsy with autonomic seizures, formerly known as Panayiotopoulos syndrome or early-onset benign occipital epilepsy

European journal of paediatric neurology, 2023-11, Vol.47, p.18-24

Oguni, Hirokazu

2023

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Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders

Brain & development (Tokyo. 1979), 2019-10, Vol.41 (9), p.776-782

2019

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Nationwide survey of glucose transporter-1 deficiency syndrome (GLUT-1DS) in Japan

Brain & development (Tokyo. 1979), 2015-09, Vol.37 (8), p.780-789

2015

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

Epilepsy research, 2019-09, Vol.155, p.106149-106149, Article 106149

2019

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Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients

PloS one, 2013-02, Vol.8 (2), p.e56120-e56120

2013

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Ketogenic diet using a Japanese ketogenic milk for patients with epilepsy: A multi-institutional study

Brain & development (Tokyo. 1979), 2018-03, Vol.40 (3), p.188-195

2018

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The role of EEG in the diagnosis and classification of the epilepsy syndromes: a tool for clinical practice by the ILAE Neurophysiology Task Force (Part 2)

Epileptic disorders, 2017-12, Vol.19 (4), p.385-437

2017

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Epilepsy with myoclonic-atonic seizures, also known as Doose syndrome: Modification of the diagnostic criteria

European journal of paediatric neurology, 2022-01, Vol.36, p.37-50

Oguni, Hirokazu

2022

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

Brain & development (Tokyo. 1979), 2021-05, Vol.43 (5), p.657-660

2021

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Recurrent NUS1 canonical splice donor site mutation in two unrelated individuals with epilepsy, myoclonus, ataxia and scoliosis - a case report

BMC neurology, 2019-10, Vol.19 (1), p.253-253, Article 253

2019

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

Brain & development (Tokyo. 1979), 2015-01, Vol.37 (1), p.18-22

2015

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Two cases of childhood narcolepsy mimicking epileptic seizures in video-EEG/EMG

Brain & development (Tokyo. 1979), 2018-11, Vol.40 (10), p.939-942

2018

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Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome

Epilepsia (Copenhagen), 2011-06, Vol.52 (6), p.1144-1149

2011

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Refractory and severe status epilepticus in a patient with ring chromosome 20 syndrome

Brain & development (Tokyo. 1979), 2016-09, Vol.38 (8), p.746-749

2016

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Mortality in Dravet syndrome: Search for risk factors in Japanese patients

Epilepsia (Copenhagen), 2011-04, Vol.52 (s2), p.50-54

2011

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Epilepsy in Children

Brain and nerve = Shinkei kenkyū no shinpo, 2023-04, Vol.75 (4), p.297

Oguni, Hirokazu

2023

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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

Brain & development (Tokyo. 1979), 2018-10, Vol.40 (9), p.813-818

2018

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Immunomodulatory therapy versus surgery for Rasmussen syndrome in early childhood

Brain & development (Tokyo. 1979), 2013-09, Vol.35 (8), p.778-785

2013

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Study of epileptic drop attacks in symptomatic epilepsy of early childhood – Differences from those in myoclonic-astatic epilepsy

Brain & development (Tokyo. 1979), 2015-01, Vol.37 (1), p.49-58

2015

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Treatment of benign focal epilepsies in children: When and how should be treated?

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

CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate

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

Outcome of ketogenic diets in GLUT1 deficiency syndrome in Japan: A nationwide survey

Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group

A reappraisal of interictal EEG characteristics in self-limited epilepsy with autonomic seizures, formerly known as Panayiotopoulos syndrome or early-onset benign occipital epilepsy

Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders

Nationwide survey of glucose transporter-1 deficiency syndrome (GLUT-1DS) in Japan

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

Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients

Ketogenic diet using a Japanese ketogenic milk for patients with epilepsy: A multi-institutional study

The role of EEG in the diagnosis and classification of the epilepsy syndromes: a tool for clinical practice by the ILAE Neurophysiology Task Force (Part 2)

Epilepsy with myoclonic-atonic seizures, also known as Doose syndrome: Modification of the diagnostic criteria

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

Recurrent NUS1 canonical splice donor site mutation in two unrelated individuals with epilepsy, myoclonus, ataxia and scoliosis - a case report

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

Two cases of childhood narcolepsy mimicking epileptic seizures in video-EEG/EMG

Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome

Refractory and severe status epilepticus in a patient with ring chromosome 20 syndrome

Mortality in Dravet syndrome: Search for risk factors in Japanese patients

Epilepsy in Children

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

Immunomodulatory therapy versus surgery for Rasmussen syndrome in early childhood

Study of epileptic drop attacks in symptomatic epilepsy of early childhood – Differences from those in myoclonic-astatic epilepsy

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