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Serial MRI findings of acute flaccid myelitis during an outbreak of enterovirus D68 infection in Japan

Brain & development (Tokyo. 1979), 2019-05, Vol.41 (5), p.443-451

2019

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Moyamoya disease susceptibility gene RNF213 links inflammatory and angiogenic signals in endothelial cells

Scientific reports, 2015-08, Vol.5 (1), p.13191-13191, Article 13191

2015

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A nation-wide survey of Japanese pediatric MOG antibody-associated diseases

Brain & development (Tokyo. 1979), 2021-06, Vol.43 (6), p.705-713

2021

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Clinical and electrophysiological features of acute flaccid myelitis: A national cohort study

Clinical neurophysiology, 2021-10, Vol.132 (10), p.2456-2463

2021

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Shank3a/b isoforms regulate the susceptibility to seizures and thalamocortical development in the early postnatal period of mice

Neuroscience research, 2023-08, Vol.193, p.13-19

2023

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A Nationwide Survey of Pediatric-onset Japanese Encephalitis in Japan

Clinical infectious diseases, 2019-05, Vol.68 (12), p.2099-2104

2019

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Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan

Brain & development (Tokyo. 1979), 2010-06, Vol.32 (6), p.454-462

2010

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Rhombencephalitis and coxsackievirus A16

Emerging infectious diseases, 2009-10, Vol.15 (10), p.1689-1691

2009

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Hyperactive mTOR signals in the proopiomelanocortin-expressing hippocampal neurons cause age-dependent epilepsy and premature death in mice

Scientific reports, 2016-03, Vol.6 (1), p.22991-22991, Article 22991

2016

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De Novo Truncating Mutation of TRIM8 Causes Early‐Onset Epileptic Encephalopathy

Annals of human genetics, 2016-07, Vol.80 (4), p.235-240

2016

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An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome

Brain & development (Tokyo. 1979), 2019-04, Vol.41 (4), p.378-381

2019

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Vaccination-associated acute disseminated encephalomyelitis

Vaccine, 2019-02, Vol.37 (8), p.1126-1129

2019

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Three-Year Longitudinal Motor Function and Disability Level of Acute Flaccid Myelitis

Pediatric neurology, 2021-03, Vol.116, p.14-19

2021

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Involuntary movements and coma as the prognostic marker for acute encephalopathy with biphasic seizures and late reduced diffusion

Journal of the neurological sciences, 2016-11, Vol.370, p.39-43

2016

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Analysis of Death Due to Infectious Diseases in Patients Hospitalized in the Pediatric Ward of a Single Japanese Tertiary Medical Facility

Japanese Journal of Infectious Diseases, 2016, Vol.69(6), pp.464-470

2016

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Sustained endocrine profiles of a girl with WAGR syndrome

BMC medical genetics, 2017-10, Vol.18 (1), p.117-117, Article 117

2017

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Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletion

Brain & development (Tokyo. 1979), 2012-11, Vol.34 (10), p.852-856

2012

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Transient dysautonomia in an acute phase of encephalopathy with biphasic seizures and late reduced diffusion

Brain & development (Tokyo. 1979), 2017-08, Vol.39 (7), p.621-624

2017

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Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes

Brain & development (Tokyo. 1979), 2014-04, Vol.36 (4), p.342-345

2014

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Strategy in short-term memory for pictures in childhood: A near-infrared spectroscopy study

NeuroImage (Orlando, Fla.), 2011-02, Vol.54 (3), p.2394-2400

2011

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PD1 as a common candidate susceptibility gene of subacute sclerosing panencephalitis

Human genetics, 2010-04, Vol.127 (4), p.411-419

2010

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A case of childhood stiff-person syndrome with striatal lesions: A possible entity distinct from the classical adult form

Brain & development (Tokyo. 1979), 2013-06, Vol.35 (6), p.575-578

2013

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Parental age and child growth and development: Child health check-up data

Pediatrics international, 2011-10, Vol.53 (5), p.709-714

2011

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Clinical and MRI characteristics of acute encephalopathy in congenital adrenal hyperplasia

Journal of the neurological sciences, 2011-07, Vol.306 (1), p.91-93

2011

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Systemic vascular phenotypes of Loeys-Dietz syndrome in a child carrying a de novo R381P mutation in TGFBR2: a case report

BMC research notes, 2013-11, Vol.6 (1), p.456-456, Article 456

2013

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Serial MRI findings of acute flaccid myelitis during an outbreak of enterovirus D68 infection in Japan

Moyamoya disease susceptibility gene RNF213 links inflammatory and angiogenic signals in endothelial cells

A nation-wide survey of Japanese pediatric MOG antibody-associated diseases

Clinical and electrophysiological features of acute flaccid myelitis: A national cohort study

Shank3a/b isoforms regulate the susceptibility to seizures and thalamocortical development in the early postnatal period of mice

A Nationwide Survey of Pediatric-onset Japanese Encephalitis in Japan

Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan

Rhombencephalitis and coxsackievirus A16

Hyperactive mTOR signals in the proopiomelanocortin-expressing hippocampal neurons cause age-dependent epilepsy and premature death in mice

De Novo Truncating Mutation of TRIM8 Causes Early‐Onset Epileptic Encephalopathy

An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome

Vaccination-associated acute disseminated encephalomyelitis

Three-Year Longitudinal Motor Function and Disability Level of Acute Flaccid Myelitis

Involuntary movements and coma as the prognostic marker for acute encephalopathy with biphasic seizures and late reduced diffusion

Analysis of Death Due to Infectious Diseases in Patients Hospitalized in the Pediatric Ward of a Single Japanese Tertiary Medical Facility

Sustained endocrine profiles of a girl with WAGR syndrome

Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletion

Transient dysautonomia in an acute phase of encephalopathy with biphasic seizures and late reduced diffusion

Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes

Strategy in short-term memory for pictures in childhood: A near-infrared spectroscopy study

PD1 as a common candidate susceptibility gene of subacute sclerosing panencephalitis

A case of childhood stiff-person syndrome with striatal lesions: A possible entity distinct from the classical adult form

Parental age and child growth and development: Child health check-up data

Clinical and MRI characteristics of acute encephalopathy in congenital adrenal hyperplasia

Systemic vascular phenotypes of Loeys-Dietz syndrome in a child carrying a de novo R381P mutation in TGFBR2: a case report

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