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Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome

Epilepsia (Copenhagen), 2012-07, Vol.53 (7), p.1140-1145

2012

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Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice

Communications biology, 2018-01, Vol.1 (1), p.96-96, Article 96

2018

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Application of High Performance Computing to Earthquake Hazard and Disaster Estimation in Urban Area

Frontiers in built environment, 2018-02, Vol.4

2018

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Three patients manifesting early infantile epileptic spasms associated with 2q24.3 microduplications

Brain & development (Tokyo. 1979), 2015-10, Vol.37 (9), p.874-879

2015

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Cutaneous adverse drug reaction in patients with epilepsy after acute encephalitis

Brain & development (Tokyo. 1979), 2012-06, Vol.34 (6), p.496-503

2012

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Functional Polymorphisms in the Promoter Regions of Matrix Metalloproteinase-2, -3, -7, -9 and TNF-alpha Genes, and the Risk of Colorectal Neoplasm in Japanese

YONAGO ACTA MEDICA, 2009-03, Vol.52 (1), p.47-56

2009

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A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome

Epilepsia (Copenhagen), 2012-12, Vol.53 (12), p.e200-e203

2012

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A homozygous mutation of voltage-gated sodium channel βI gene SCN1B in a patient with Dravet syndrome

Epilepsia (Copenhagen), 2012-12, Vol.53 (12), p.e200-e203

2012

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Gastric metastasis by primary lung adenocarcinoma

World journal of gastrointestinal oncology, 2010-10, Vol.2 (10), p.395-398

2010

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CDKL5 deficiency causes epileptic seizures independent of cellular mosaicism

Journal of the neurological sciences, 2022-12, Vol.443, p.120498-120498, Article 120498

2022

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Dose-dependent teratogenicity of valproate in mono- and polytherapy: an observational study

Neurology, 2015-09, Vol.85 (10), p.866

2015

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Stiripentol open study in Japanese patients with Dravet syndrome

Epilepsia (Copenhagen), 2009-11, Vol.50 (11), p.2362-2368

2009

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Deletions of SCN1A 5′ genomic region with promoter activity in Dravet syndrome

Human mutation, 2010-07, Vol.31 (7), p.820-829

2010

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Individualized phenytoin therapy for Japanese pediatric patients with epilepsy based on CYP2C9 and CYP2C19 genotypes

Therapeutic drug monitoring, 2015-04, Vol.37 (2), p.229

2015

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Early predictors of status epilepticus-associated mortality and morbidity in children

Brain & development (Tokyo. 1979), 2015-05, Vol.37 (5), p.478-486

2015

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Sleepiness:a frequent adverse reaction of antiepileptic drugs in patients with epilepsy after encephalitis/encephalopathy

No to hattatsu, 2012-11, Vol.44 (6), p.472

2012

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Reversible posterior leukoencephalopathy in a patient with Wegener granulomatosis

Pediatric nephrology (Berlin, West), 2004-04, Vol.19 (4), p.442-444

2004

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Effectiveness of topiramate in eleven patients with Dravet syndrome

No to hattatsu, 2010-07, Vol.42 (4), p.273

2010

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Association of Functional Gene Polymorphisms of Interleukin-1β and Transforming Growth Factor-β1 with the Progression of Liver Fibrosis in Japanese Patients with Hepatitis C Virus-Related Chronic Liver Disease

YONAGO ACTA MEDICA, 2007, Vol.50 (4), p.89-97

2007

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A Case of Tubulointerstitial Nephritis and Uveitis Syndrome

Japanese journal of pediatric nephrology, 2007/04/15, Vol.20(1), pp.31-34

2007

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Efficient serial episode mining with minimal occurrences

Proceedings of the 3rd International Conference on Ubiquitous Information Management and Communication, 2009, p.457-464

2009

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TINU症候群の1例

日本小児腎臓病学会雑誌, 2007/04/15, Vol.20(1), pp.31-34

2007

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Development of Industrial Control Programming Environment Enhanced by Extensible Graphic Symbols

2006 SICE-ICASE International Joint Conference, 2006, p.5169-5172

2006

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Refractory Ventricular Arrhythmias in a Patient With Dilated Cardiomyopathy Caused by a Nonsense Mutation in BAG5

Circulation Journal, 2022/11/25, Vol.86(12), pp.2043

2022

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Exploring a legendary giant squid: an environmental DNA approach

Marine biology, 2020-10, Vol.167 (11), Article 160

2020

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Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome

Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice

Application of High Performance Computing to Earthquake Hazard and Disaster Estimation in Urban Area

Three patients manifesting early infantile epileptic spasms associated with 2q24.3 microduplications

Cutaneous adverse drug reaction in patients with epilepsy after acute encephalitis

Functional Polymorphisms in the Promoter Regions of Matrix Metalloproteinase-2, -3, -7, -9 and TNF-alpha Genes, and the Risk of Colorectal Neoplasm in Japanese

A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome

A homozygous mutation of voltage-gated sodium channel βI gene SCN1B in a patient with Dravet syndrome

Gastric metastasis by primary lung adenocarcinoma

CDKL5 deficiency causes epileptic seizures independent of cellular mosaicism

Dose-dependent teratogenicity of valproate in mono- and polytherapy: an observational study

Stiripentol open study in Japanese patients with Dravet syndrome

Deletions of SCN1A 5′ genomic region with promoter activity in Dravet syndrome

Individualized phenytoin therapy for Japanese pediatric patients with epilepsy based on CYP2C9 and CYP2C19 genotypes

Early predictors of status epilepticus-associated mortality and morbidity in children

Sleepiness:a frequent adverse reaction of antiepileptic drugs in patients with epilepsy after encephalitis/encephalopathy

Reversible posterior leukoencephalopathy in a patient with Wegener granulomatosis

Effectiveness of topiramate in eleven patients with Dravet syndrome

Association of Functional Gene Polymorphisms of Interleukin-1β and Transforming Growth Factor-β1 with the Progression of Liver Fibrosis in Japanese Patients with Hepatitis C Virus-Related Chronic Liver Disease

A Case of Tubulointerstitial Nephritis and Uveitis Syndrome

Efficient serial episode mining with minimal occurrences

TINU症候群の1例

Development of Industrial Control Programming Environment Enhanced by Extensible Graphic Symbols

Refractory Ventricular Arrhythmias in a Patient With Dilated Cardiomyopathy Caused by a Nonsense Mutation in BAG5

Exploring a legendary giant squid: an environmental DNA approach

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