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Management of and prophylaxis against status epilepticus in children with severe myoclonic epilepsy in infancy (SMEI; Dravet syndrome) – A nationwide questionnaire survey in Japan

Brain & development (Tokyo. 1979), 2008-11, Vol.30 (10), p.629-635

2008

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A pilot study on the changes in immunity after ACTH therapy in patients with West syndrome

Brain & development (Tokyo. 1979), 2009-11, Vol.31 (10), p.739-743

2009

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Survey of Japanese pediatricians on vaccination of children with neurological disorders

Pediatrics international, 2011-10, Vol.53 (5), p.626-629

2011

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Founders of child neurology in Japan—Kihei Maekawa

Brain & development (Tokyo. 1979), 2005, Vol.27 (1), p.3-4

2005

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Characteristics of gene mutations among 32 unrelated Japanese Gaucher disease patients : absence of the common Jewish 84GG and 1226G mutations

Human genetics, 1995-06, Vol.95 (6), p.717-720

1995

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Dermal testing of vaccines for children at high risk of allergies

Vaccine, 2007-04, Vol.25 (17), p.3454-3463

2007

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Survey of vaccination and viral infections for children with severe myoclonic epilepsy in infancy

No to hattatsu, 2004-07, Vol.36 (4), p.318

2004

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Intravenous gammaglobulin therapy of Satoyoshi syndrome

Brain & development (Tokyo. 1979), 1996-09, Vol.18 (5), p.409-411

1996

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Early intervention for very-low-birth-weight infants

Brain & development (Tokyo. 1979), 1998, Vol.20 (1), p.18-21

1998

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Long‐term follow up of abdominal aortic aneurysm complicating Kawasaki disease: Comparison of the effectiveness of different imaging methods

Pediatrics international, 1996-06, Vol.38 (3), p.252-255

1996

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A japanese patient with X-linked α-thalassemia/mental retardation syndrome: An additional case report

Jinrui idengaku zasshi. Japanese journal of human genetics, 1996-09, Vol.41 (3), p.329-332

1996

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A patient with epilepsy, congenital alopecia and mental retardation: combination of atypical absence in waking and nocturnal partial seizure

No to hattatsu, 2000-07, Vol.32 (4), p.312

2000

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Abnormal urinary excretion of polyamines in HHH syndrome (hyperornithinemia associated with hyperammonemia and homocitrullinuria)

Brain & development (Tokyo. 1979), 1990, Vol.12 (5), p.533-535

1990

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Acute disseminated encephalomyelitis after treatment with Japanese B encephalitis vaccine (Nakayama-Yoken and Beijing strains)

Journal of neurology, neurosurgery and psychiatry, 1995-09, Vol.59 (3), p.316-317

1995

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Childhood multiple sclerosis and allied demyelinative diseases

No to hattatsu, 1999-01, Vol.31 (1), p.44

1999

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Topography, size and number of cortical tubers in tuberous sclerosis with West syndrome

No to hattatsu, 1998-03, Vol.30 (2), p.152

1998

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Developmental change of sucking response to taste in infants

Biology of the neonate, 1991, Vol.60 Suppl 1 (Suppl. 1), p.62-74

1991

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Fulminant subacute sclerosing panencephalitis: clinical and neuropathological observations

No to hattatsu, 1997-11, Vol.29 (6), p.494

1997

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A case of benign childhood epilepsy with centrotemporal spike diagnosed by a seizure during polysomnography and clinical and EEG follow-up

No to hattatsu, 1993-11, Vol.25 (6), p.563

1993

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Development of standing and walking evaluated by the center of gravity

No to hattatsu, 1988-03, Vol.20 (2), p.91

Maekawa, K

1988

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A Study of Atypical Benign Partial Epilepsy of Childhood (ABPE) by Means of Long Term EEG Recording

Tenkan kenkyū, 1994, Vol.12 (1), p.23-27

1994

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Psychiatric inpatients and chromosome deletions within 22q11.2

Journal of neurology, neurosurgery and psychiatry, 1999-12, Vol.67 (6), p.803-806

1999

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High-dose immunoglobulin therapy for Guillain−Barré syndrome in Japanese children

Pediatrics international, 2003-10, Vol.45 (5), p.543-549

2003

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MRI findings of anterior spinal artery syndrome in childhood

No to hattatsu, 1996-09, Vol.28 (5), p.438

1996

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A possible same genetic defect in two Niemann-Pick disease model mice

No to hattatsu, 1994-07, Vol.26 (4), p.318

1994

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Management of and prophylaxis against status epilepticus in children with severe myoclonic epilepsy in infancy (SMEI; Dravet syndrome) – A nationwide questionnaire survey in Japan

A pilot study on the changes in immunity after ACTH therapy in patients with West syndrome

Survey of Japanese pediatricians on vaccination of children with neurological disorders

Founders of child neurology in Japan—Kihei Maekawa

Characteristics of gene mutations among 32 unrelated Japanese Gaucher disease patients : absence of the common Jewish 84GG and 1226G mutations

Dermal testing of vaccines for children at high risk of allergies

Survey of vaccination and viral infections for children with severe myoclonic epilepsy in infancy

Intravenous gammaglobulin therapy of Satoyoshi syndrome

Early intervention for very-low-birth-weight infants

Long‐term follow up of abdominal aortic aneurysm complicating Kawasaki disease: Comparison of the effectiveness of different imaging methods

A japanese patient with X-linked α-thalassemia/mental retardation syndrome: An additional case report

A patient with epilepsy, congenital alopecia and mental retardation: combination of atypical absence in waking and nocturnal partial seizure

Abnormal urinary excretion of polyamines in HHH syndrome (hyperornithinemia associated with hyperammonemia and homocitrullinuria)

Acute disseminated encephalomyelitis after treatment with Japanese B encephalitis vaccine (Nakayama-Yoken and Beijing strains)

Childhood multiple sclerosis and allied demyelinative diseases

Topography, size and number of cortical tubers in tuberous sclerosis with West syndrome

Developmental change of sucking response to taste in infants

Fulminant subacute sclerosing panencephalitis: clinical and neuropathological observations

A case of benign childhood epilepsy with centrotemporal spike diagnosed by a seizure during polysomnography and clinical and EEG follow-up

Development of standing and walking evaluated by the center of gravity

A Study of Atypical Benign Partial Epilepsy of Childhood (ABPE) by Means of Long Term EEG Recording

Psychiatric inpatients and chromosome deletions within 22q11.2

High-dose immunoglobulin therapy for Guillain−Barré syndrome in Japanese children

MRI findings of anterior spinal artery syndrome in childhood

A possible same genetic defect in two Niemann-Pick disease model mice

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