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Classification of pediatric headache cases referred to a neurology department

Pediatrics international, 2022-01, Vol.64 (1), p.e15181-n/a

2022

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Post coronavirus disease 2019 condition in children at a children's hospital in Japan

Pediatrics international, 2023-01, Vol.65 (1), p.e15458-n/a

2023

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Rituximab treatment for a child with antibody‐negative limbic encephalitis

Pediatrics international, 2022-01, Vol.64 (1), p.e15287-n/a

2022

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Sinus pericranii associated with syntelencephaly: a case report

BMC neurology, 2022-08, Vol.22 (1), p.1-316, Article 316

2022

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Refractory cerebral infarction in a child with an ACTA2 mutation

Brain & development (Tokyo. 1979), 2021-04, Vol.43 (4), p.585-589

2021

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White matter abnormality in Jacobsen syndrome assessed by serial MRI

Brain & development (Tokyo. 1979), 2020-09, Vol.42 (8), p.621-625

2020

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Nonsense variants in STAG2 result in distinct sex-dependent phenotypes

Journal of human genetics, 2019-05, Vol.64 (5), p.487-492

2019

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Intermittent Erythema in Guillain-Barré Syndrome

Pediatric neurology, 2018-07, Vol.84, p.56-56

2018

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Retrospective Echocardiographic Analysis of West Syndrome During Adrenocorticotropic Hormone Therapy

Frontiers in pediatrics, 2022-05, Vol.10, p.889752-889752

2022

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Retraction Note to: Nonsense variants in STAG2 result in distinct sex-dependent phenotypes

Journal of human genetics, 2020-09, Vol.65 (9), p.811-811

2020

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Nonsense variants of STAG2 result in distinct congenital anomalies

Human genome variation, 2020-09, Vol.7 (1), p.26-26, Article 26

2020

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Coma and seizure caused by an afloqualone overdose

Pediatrics international, 2019-02, Vol.61 (2), p.212-213

2019

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Diagnostic use of computational retrotransposon detection: Successful definition of pathogenetic mechanism in a ciliopathy phenotype

American journal of medical genetics. Part A, 2017-05, Vol.173 (5), p.1353-1357

2017

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The Absence of Later Wave Components in Auditory Brainstem Responses as an Initial Manifestation of Type 2 Gaucher Disease

Pediatric neurology, 2014-12, Vol.51 (6), p.837-839

2014

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Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth disease

Annals of neurology, 2012-01, Vol.71 (1), p.84-92

2012

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Afebrile seizures associated with respiratory syncytial virus infection: A situation‐related seizure disorder in early infancy

Pediatrics international, 2011-02, Vol.53 (1), p.113-115

2011

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The Utility of Limited-Montage Electroencephalography for Seizure Detection in Children

Pediatric neurology, 2022-12, Vol.137, p.1-5

2022

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Children with posterior reversible encephalopathy syndrome associated with atypical diffusion-weighted imaging and apparent diffusion coefficient

Clinical and experimental nephrology, 2011-04, Vol.15 (2), p.275-280

2011

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Generalized Nonconvulsive Status Epilepticus in Symptomatic Partial Epilepsy

Pediatric neurology, 2007-03, Vol.36 (3), p.195-198

Miyama, Sahoko, MD

2007

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Status Epilepticus due to Asfotase Alfa Interruption in Perinatal Severe Hypophosphatasia

Pediatric neurology, 2022-05, Vol.130, p.4-6

2022

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Recurrent Lingual Abscess in a Child

The Pediatric infectious disease journal, 2017-07, Vol.36 (7), p.694-695

2017

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Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37‐PACS1‐PACS2 axis

American journal of medical genetics. Part A, 2021-03, Vol.185 (3), p.884-888

2021

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Monozygotic Twins With Severe Myoclonic Epilepsy in Infancy Discordant for Clinical Features

Pediatric neurology, 2008-08, Vol.39 (2), p.120-122

2008

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Infantile Hypoxic Encephalopathy Mimicking Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion (AESD) Identified as an Episode of Brief Resolved Unexplained Event (BRUE)

Journal of clinical medicine, 2023-08, Vol.12 (16), p.5239

2023

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Infantile Hypoxic Encephalopathy Mimicking Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion

Journal of clinical medicine, 2023-08, Vol.12 (16)

2023

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Classification of pediatric headache cases referred to a neurology department

Post coronavirus disease 2019 condition in children at a children's hospital in Japan

Rituximab treatment for a child with antibody‐negative limbic encephalitis

Sinus pericranii associated with syntelencephaly: a case report

Refractory cerebral infarction in a child with an ACTA2 mutation

White matter abnormality in Jacobsen syndrome assessed by serial MRI

Nonsense variants in STAG2 result in distinct sex-dependent phenotypes

Intermittent Erythema in Guillain-Barré Syndrome

Retrospective Echocardiographic Analysis of West Syndrome During Adrenocorticotropic Hormone Therapy

Retraction Note to: Nonsense variants in STAG2 result in distinct sex-dependent phenotypes

Nonsense variants of STAG2 result in distinct congenital anomalies

Coma and seizure caused by an afloqualone overdose

Diagnostic use of computational retrotransposon detection: Successful definition of pathogenetic mechanism in a ciliopathy phenotype

The Absence of Later Wave Components in Auditory Brainstem Responses as an Initial Manifestation of Type 2 Gaucher Disease

Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth disease

Afebrile seizures associated with respiratory syncytial virus infection: A situation‐related seizure disorder in early infancy

The Utility of Limited-Montage Electroencephalography for Seizure Detection in Children

Children with posterior reversible encephalopathy syndrome associated with atypical diffusion-weighted imaging and apparent diffusion coefficient

Generalized Nonconvulsive Status Epilepticus in Symptomatic Partial Epilepsy

Status Epilepticus due to Asfotase Alfa Interruption in Perinatal Severe Hypophosphatasia

Recurrent Lingual Abscess in a Child

Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37‐PACS1‐PACS2 axis

Monozygotic Twins With Severe Myoclonic Epilepsy in Infancy Discordant for Clinical Features

Infantile Hypoxic Encephalopathy Mimicking Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion (AESD) Identified as an Episode of Brief Resolved Unexplained Event (BRUE)

Infantile Hypoxic Encephalopathy Mimicking Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion

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