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Multiple cerebral cysts are another possible feature of Jacobsen syndrome

Brain & development (Tokyo. 1979), 2020-09, Vol.42 (8), p.626-626

2020

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Rhinovirus-associated acute encephalitis/encephalopathy and cerebellitis

Brain & development (Tokyo. 1979), 2019-06, Vol.41 (6), p.551-554

2019

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De novo KCNT1 mutations in early‐onset epileptic encephalopathy

Epilepsia (Copenhagen), 2015-09, Vol.56 (9), p.e121-e128

2015

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Acute encephalopathy with biphasic seizures and late reduced diffusion; posterior frontal hyperperfusion before late seizures revealed by arterial spin labeling: A case report

Brain & development (Tokyo. 1979), 2021-06, Vol.43 (6), p.714-718

2021

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Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy

Brain & development (Tokyo. 1979), 2019-11, Vol.41 (10), p.862-869

2019

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Acute encephalopathy in children with tuberous sclerosis complex

Orphanet journal of rare diseases, 2021-01, Vol.16 (1), p.5-5, Article 5

2021

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Protein-Losing Enteropathy as a Rare Complication of the Ketogenic Diet

Pediatric neurology, 2015-05, Vol.52 (5), p.526-528

2015

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Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases

Brain & development (Tokyo. 1979), 2011-06, Vol.33 (6), p.512-517

2011

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Interstitial deletions in the proximal regions of 6q: 12 original cases and a literature review

Intractable & Rare Diseases Research, 2022/08/31, Vol.11(3), pp.143-148

2022

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Severe pediatric acute encephalopathy syndromes related to SARS-CoV-2

Frontiers in neuroscience, 2023-02, Vol.17, p.1085082-1085082

2023

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Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor δ2 autoantibody

Brain & development (Tokyo. 1979), 2007-05, Vol.29 (4), p.254-256

2007

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Asymptomatic congenital cytomegalovirus infection with neurological sequelae: A retrospective study using umbilical cord

Brain & development (Tokyo. 1979), 2016-10, Vol.38 (9), p.819-826

2016

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A mild case of giant axonal neuropathy without central nervous system manifestation

Brain & development (Tokyo. 1979), 2016-03, Vol.38 (3), p.350-353

2016

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De novo variants in CAMK2A and CAMK2B cause neurodevelopmental disorders

Annals of clinical and translational neurology, 2018-03, Vol.5 (3), p.280-296

2018

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A case of mumps-related acute encephalopathy with biphasic seizures and late reduced diffusion

Brain & development (Tokyo. 1979), 2017-10, Vol.39 (9), p.808-810

2017

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Another case of respiratory syncytial virus-related limbic encephalitis

Neuroradiology, 2014-05, Vol.56 (5), p.435-436

2014

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Rotavirus associated acute encephalitis/encephalopathy and concurrent cerebellitis: Report of two cases

Brain & development (Tokyo. 1979), 2007-11, Vol.29 (10), p.670-673

2007

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A novel PLP1 frameshift mutation causing a milder form of Pelizaeus–Merzbacher disease

Brain & development (Tokyo. 1979), 2015-04, Vol.37 (4), p.455-458

2015

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Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34

Brain & development (Tokyo. 1979), 2015-08, Vol.37 (7), p.714-718

2015

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Mucolipidosis IV: A milder form with novel mutations and serial MRI findings

Brain & development (Tokyo. 1979), 2016-09, Vol.38 (8), p.763-767

2016

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Early infantile manifestations of incontinentia pigmenti mimicking acute encephalopathy

Brain & development (Tokyo. 1979), 2011-01, Vol.33 (1), p.28-34

2011

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Peripheral lymphocyte subset and serum cytokine profiles of patients with West syndrome

Brain & development (Tokyo. 1979), 2010-10, Vol.32 (9), p.695-702

2010

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Serum and CSF biomarkers in acute pediatric neurological disorders

Brain & development (Tokyo. 1979), 2014-06, Vol.36 (6), p.489-495

2014

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Respiratory syncytial virus‐associated encephalopathy complicated by congenital myopathy

Pediatrics international, 2012-10, Vol.54 (5), p.709-711

2012

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Abnormal glucose metabolism in aromatic l -amino acid decarboxylase deficiency

Brain & development (Tokyo. 1979), 2010-06, Vol.32 (6), p.506-510

2010

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Multiple cerebral cysts are another possible feature of Jacobsen syndrome

Rhinovirus-associated acute encephalitis/encephalopathy and cerebellitis

De novo KCNT1 mutations in early‐onset epileptic encephalopathy

Acute encephalopathy with biphasic seizures and late reduced diffusion; posterior frontal hyperperfusion before late seizures revealed by arterial spin labeling: A case report

Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy

Acute encephalopathy in children with tuberous sclerosis complex

Protein-Losing Enteropathy as a Rare Complication of the Ketogenic Diet

Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases

Interstitial deletions in the proximal regions of 6q: 12 original cases and a literature review

Severe pediatric acute encephalopathy syndromes related to SARS-CoV-2

Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor δ2 autoantibody

Asymptomatic congenital cytomegalovirus infection with neurological sequelae: A retrospective study using umbilical cord

A mild case of giant axonal neuropathy without central nervous system manifestation

De novo variants in CAMK2A and CAMK2B cause neurodevelopmental disorders

A case of mumps-related acute encephalopathy with biphasic seizures and late reduced diffusion

Another case of respiratory syncytial virus-related limbic encephalitis

Rotavirus associated acute encephalitis/encephalopathy and concurrent cerebellitis: Report of two cases

A novel PLP1 frameshift mutation causing a milder form of Pelizaeus–Merzbacher disease

Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34

Mucolipidosis IV: A milder form with novel mutations and serial MRI findings

Early infantile manifestations of incontinentia pigmenti mimicking acute encephalopathy

Peripheral lymphocyte subset and serum cytokine profiles of patients with West syndrome

Serum and CSF biomarkers in acute pediatric neurological disorders

Respiratory syncytial virus‐associated encephalopathy complicated by congenital myopathy

Abnormal glucose metabolism in aromatic l -amino acid decarboxylase deficiency

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