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A long‐term follow‐up study of Dravet syndrome up to adulthood

Epilepsia (Copenhagen), 2010-06, Vol.51 (6), p.1043-1052

2010

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Scalp‐recorded high‐frequency oscillations in childhood sleep‐induced electrical status epilepticus

Epilepsia (Copenhagen), 2010-10, Vol.51 (10), p.2190-2194

2010

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Long-term safety and efficacy of stiripentol for the treatment of Dravet syndrome: A multicenter, open-label study in Japan

Epilepsy research, 2015-07, Vol.113, p.90-97

2015

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High‐frequency oscillations in idiopathic partial epilepsy of childhood

Epilepsia (Copenhagen), 2011-10, Vol.52 (10), p.1812-1819

2011

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Predictive factors for relapse of epileptic spasms after adrenocorticotropic hormone therapy in West syndrome

Brain & development (Tokyo. 1979), 2016-01, Vol.38 (1), p.32-39

2016

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Predicting the reading skill of Japanese children

Brain & development (Tokyo. 1979), 2017-02, Vol.39 (2), p.112-121

2017

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Rufinamide as an adjunctive therapy for Lennox–Gastaut syndrome: A randomized double-blind placebo-controlled trial in Japan

Epilepsy research, 2014-11, Vol.108 (9), p.1627-1636

2014

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The Rey–Osterrieth Complex Figure as a measure of executive function in childhood

Brain & development (Tokyo. 1979), 2005-12, Vol.27 (8), p.564-569

2005

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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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Long-term efficacy and safety of lamotrigine monotherapy in Japanese and South Korean pediatric patients with newly diagnosed typical absence seizures: An open-label extension study

Brain & development (Tokyo. 1979), 2018-10, Vol.40 (9), p.786-791

2018

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Treatment of epilepsy with electrical status epilepticus during slow sleep and its related disorders

Brain & development (Tokyo. 1979), 2006-06, Vol.28 (5), p.281-286

2006

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Efficacy and safety of vigabatrin in Japanese patients with infantile spasms: Primary short-term study and extension study

Epilepsy & behavior, 2018-01, Vol.78, p.134-141

Ohtsuka, Yoko

2018

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CACNA1A variants may modify the epileptic phenotype of Dravet syndrome

Neurobiology of disease, 2013-02, Vol.50, p.209-217

2013

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Executive function in children with pervasive developmental disorder and attention-deficit/hyperactivity disorder assessed by the Keio version of the Wisconsin card sorting test

Brain & development (Tokyo. 1979), 2012-05, Vol.34 (5), p.354-359

2012

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A Screening test for the prediction of Dravet syndrome before one year of age

Epilepsia (Copenhagen), 2008-04, Vol.49 (4), p.626-633

2008

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Occurrence of bilaterally independent epileptic spasms after a corpus callosotomy in West syndrome

Brain & development (Tokyo. 1979), 2016-01, Vol.38 (1), p.132-135

2016

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Prevalence of Childhood Epilepsy and Distribution of Epileptic Syndromes: A Population‐based Survey in Okayama, Japan

Epilepsia (Copenhagen), 2006-03, Vol.47 (3), p.626-630

2006

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Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy

Biochemical and biophysical research communications, 2002-07, Vol.295 (1), p.17-23

2002

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Are pervasive developmental disorders and attention-deficit/hyperactivity disorder distinct disorders?

Brain & development (Tokyo. 1979), 2006-07, Vol.28 (6), p.371-374

2006

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Amelioration of disabling myoclonus in a case of DRPLA by levetiracetam

Brain & development (Tokyo. 1979), 2012-05, Vol.34 (5), p.368-371

2012

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Oxcarbazepine adjunctive therapy for partial seizures in Japanese pediatric patients: a randomized double-blind placebo-controlled study and open-label extension study

Epilepsy & Seizure, 2019, Vol.11(1), pp.30-45

2019

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Vitamin B 6 treatment of intractable seizures

Brain & development (Tokyo. 1979), 2011-10, Vol.33 (9), p.783-789

2011

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Dipole Modeling of Epileptic Spikes Can Be Accurate or Misleading

Epilepsia (Copenhagen), 2005-03, Vol.46 (3), p.397-408

2005

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Dravet syndrome: a genetic epileptic disorder

Acta medica Okayama, 2012-10, Vol.66 (5), p.369-376

2012

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High-frequency EEG activity in epileptic encephalopathy with suppression-burst

Brain & development (Tokyo. 1979), 2015-02, Vol.37 (2), p.230-236

2015

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A long‐term follow‐up study of Dravet syndrome up to adulthood

Scalp‐recorded high‐frequency oscillations in childhood sleep‐induced electrical status epilepticus

Long-term safety and efficacy of stiripentol for the treatment of Dravet syndrome: A multicenter, open-label study in Japan

High‐frequency oscillations in idiopathic partial epilepsy of childhood

Predictive factors for relapse of epileptic spasms after adrenocorticotropic hormone therapy in West syndrome

Predicting the reading skill of Japanese children

Rufinamide as an adjunctive therapy for Lennox–Gastaut syndrome: A randomized double-blind placebo-controlled trial in Japan

The Rey–Osterrieth Complex Figure as a measure of executive function in childhood

Immunomodulatory therapy versus surgery for Rasmussen syndrome in early childhood

Long-term efficacy and safety of lamotrigine monotherapy in Japanese and South Korean pediatric patients with newly diagnosed typical absence seizures: An open-label extension study

Treatment of epilepsy with electrical status epilepticus during slow sleep and its related disorders

Efficacy and safety of vigabatrin in Japanese patients with infantile spasms: Primary short-term study and extension study

CACNA1A variants may modify the epileptic phenotype of Dravet syndrome

Executive function in children with pervasive developmental disorder and attention-deficit/hyperactivity disorder assessed by the Keio version of the Wisconsin card sorting test

A Screening test for the prediction of Dravet syndrome before one year of age

Occurrence of bilaterally independent epileptic spasms after a corpus callosotomy in West syndrome

Prevalence of Childhood Epilepsy and Distribution of Epileptic Syndromes: A Population‐based Survey in Okayama, Japan

Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy

Are pervasive developmental disorders and attention-deficit/hyperactivity disorder distinct disorders?

Amelioration of disabling myoclonus in a case of DRPLA by levetiracetam

Oxcarbazepine adjunctive therapy for partial seizures in Japanese pediatric patients: a randomized double-blind placebo-controlled study and open-label extension study

Vitamin B 6 treatment of intractable seizures

Dipole Modeling of Epileptic Spikes Can Be Accurate or Misleading

Dravet syndrome: a genetic epileptic disorder

High-frequency EEG activity in epileptic encephalopathy with suppression-burst

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