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The Japanese scheme of ACTH therapy in West syndrome

Epilepsia (Copenhagen), 2010-10, Vol.51 (10), p.2216-2218

Fukuyama, Yukio

2010

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Benign Familial Infantile Convulsions: Linkage to Chromosome 16p12‐q12 in 14 Families

Epilepsia (Copenhagen), 2004-06, Vol.45 (6), p.601-609

2004

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Rasmussen Syndrome: Multifocal Spread of Inflammation Suggested from MRI and PET Findings

Epilepsia (Copenhagen), 2003-08, Vol.44 (8), p.1118-1121

2003

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Fukutin gene retrotransposal insertion in a non-Japanese Fukuyama congenital muscular dystrophy (FCMD) patient

American journal of medical genetics. Part A, 2009-11, Vol.149A (11), p.2403-2408

2009

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Extraordinary halocarbon emissions initiated by the 2011 Tohoku earthquake

Geophysical research letters, 2015-04, Vol.42 (7), p.2500-2507

2015

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Projection of Climatic Change over Japan Due to Global Warming by High-Resolution Regional Climate Model in MRI

SOLA, 2005, Vol.1, pp.97-100

2005

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Severe myoclonic epilepsy in infancy: Dravet syndrome

Advances in neurology, 2005, Vol.95, p.71

2005

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Bias corrections of GOSAT SWIR XCO2 and XCH4 with TCCON data and their evaluation using aircraft measurement data

Atmospheric measurement techniques, 2016-08, Vol.9 (8), p.3491-3512

2016

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The whole story of discovery of Fukuyama congenital muscular dystrophy

Rinshō shinkeigaku, 2007-11, Vol.47 (11), p.739

Fukuyama, Yukio

2007

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Fukuyama congenital muscular dystrophy--history and perspectives

Brain and nerve = Shinkei kenkyū no shinpo, 2008-01, Vol.60 (1), p.43

Fukuyama, Yukio

2008

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Ataxia-ocular motor aprilaxia: A syndrome mimicking ataxia-telangiectasia

Annals of neurology, 1988-10, Vol.24 (4), p.497-502

1988

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Bias corrections of GOSAT SWIR XCO 2 and XCH 4 with TCCON data and their evaluation using aircraft measurement data

Atmospheric measurement techniques, 2016-08, Vol.9 (8), p.3491-3512

2016

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Bias corrections of GOSAT SWIR XCO.sub.2 and XCH.sub.4 with TCCON data and their evaluation using aircraft measurement data

Atmospheric measurement techniques, 2016-08, Vol.9 (8), p.3491

2016

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A Study of Unilateral Brief Focal Atonia in Childhood Partial Epilepsy

Epilepsia (Copenhagen), 1992-01, Vol.33 (1), p.75-83

1992

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Chronic Localized Encephalitis (Rasmussen's Syndrome) Preceded by Ipsilateral Uveitis: A Case Report

Epilepsia (Copenhagen), 1994-11, Vol.35 (6), p.1328-1331

1994

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Contribution of Japanese researchers to progress in the field of neurology in the last 100 years: Congenital progressive muscular dystrophy

Nihon Naika Gakkai zasshi, 2002-08, Vol.91 (8), p.2321-2324

Fukuyama, Yukio

2002

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Incidence of Subacute Sclerosing Panencephalitis Following Measles and Measles Vaccination in Japan

International journal of epidemiology, 1989-09, Vol.18 (3), p.684-689

1989

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Acute non-herpetic encephalitis with severe refractory status epilepticus --its overwhelming ictogenicity, epileptogenicity, long-term prognosis and review of the literature

No to hattatsu, 2007-03, Vol.39 (2), p.138

2007

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Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort

Advances in neurology, 2005, Vol.95, p.103

2005

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Neuronal Migration Disorders and Their Impact on Pediatric Epileptology

Journal of child neurology, 2005-04, Vol.20 (4), p.273-273

2005

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Neuronal Migration Disorders and Their Impact on Pediatric Epileptology

Journal of child neurology, 2004-03, Vol.19 (3), p.273-273

2004

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Status epilepticus in infants and young children: Basic mechanisms, clinical evaluation, prognosis and treatment

Acta neurologica Scandinavica. Supplementum, 2007, Vol.115 (186)

2007

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A case of acute theophylline intoxication with repeated status convulsivus

No to hattatsu, 1999-11, Vol.31 (6), p.559

1999

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Fukuyama Type Congenital Progressive Muscular Dystrophy

Acta paediatrica Japonica. Overseas edition, 1991-04, Vol.33 (2), p.261-269

1991

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PRRT2 Mutations are the major cause of benign familial infantile seizures

The Japanese scheme of ACTH therapy in West syndrome

Benign Familial Infantile Convulsions: Linkage to Chromosome 16p12‐q12 in 14 Families

Rasmussen Syndrome: Multifocal Spread of Inflammation Suggested from MRI and PET Findings

Fukutin gene retrotransposal insertion in a non-Japanese Fukuyama congenital muscular dystrophy (FCMD) patient

Extraordinary halocarbon emissions initiated by the 2011 Tohoku earthquake

Projection of Climatic Change over Japan Due to Global Warming by High-Resolution Regional Climate Model in MRI

Severe myoclonic epilepsy in infancy: Dravet syndrome

Bias corrections of GOSAT SWIR XCO2 and XCH4 with TCCON data and their evaluation using aircraft measurement data

The whole story of discovery of Fukuyama congenital muscular dystrophy

Fukuyama congenital muscular dystrophy--history and perspectives

Ataxia-ocular motor aprilaxia: A syndrome mimicking ataxia-telangiectasia

Bias corrections of GOSAT SWIR XCO 2 and XCH 4 with TCCON data and their evaluation using aircraft measurement data

Bias corrections of GOSAT SWIR XCO.sub.2 and XCH.sub.4 with TCCON data and their evaluation using aircraft measurement data

A Study of Unilateral Brief Focal Atonia in Childhood Partial Epilepsy

Chronic Localized Encephalitis (Rasmussen's Syndrome) Preceded by Ipsilateral Uveitis: A Case Report

Contribution of Japanese researchers to progress in the field of neurology in the last 100 years: Congenital progressive muscular dystrophy

Incidence of Subacute Sclerosing Panencephalitis Following Measles and Measles Vaccination in Japan

Acute non-herpetic encephalitis with severe refractory status epilepticus --its overwhelming ictogenicity, epileptogenicity, long-term prognosis and review of the literature

Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort

Neuronal Migration Disorders and Their Impact on Pediatric Epileptology

Neuronal Migration Disorders and Their Impact on Pediatric Epileptology

Status epilepticus in infants and young children: Basic mechanisms, clinical evaluation, prognosis and treatment

A case of acute theophylline intoxication with repeated status convulsivus

Fukuyama Type Congenital Progressive Muscular Dystrophy

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