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Erythema nodosum as the initial symptom of Crohn's disease: A case report

Pediatrics international, 2023-01, Vol.65 (1), p.e15626-n/a

2023

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De novo GABRA1 mutations in Ohtahara and West syndromes

Epilepsia (Copenhagen), 2016-04, Vol.57 (4), p.566-573

2016

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Glabellar ecchymosis and headache: Variations of pain‐associated ecchymosis

Psychiatry and clinical neurosciences, 2015-06, Vol.69 (6), p.385-385

2015

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Novel missense mutation in CLN8 in late infantile neuronal ceroid lipofuscinosis: The first report of a CLN8 mutation in Japan

Brain & development (Tokyo. 1979), 2016-03, Vol.38 (3), p.341-345

2016

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Neuroepidemiology of Porencephaly, Schizencephaly, and Hydranencephaly in Miyagi Prefecture, Japan

Pediatric neurology, 2016, Vol.54, p.39-42.e1

2016

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Human Herpes Virus Type 6 Can Cause Skin Lesions at the BCG Inoculation Site Similar to Kawasaki Disease

The Tohoku Journal of Experimental Medicine, 2012, Vol.228(4), pp.351-353

2012

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Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy

Brain & development (Tokyo. 1979), 2019-10, Vol.41 (9), p.790-795

2019

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A female case of West syndrome with remission of spasms following multiple cerebral hemorrhages

Brain & development (Tokyo. 1979), 2011-09, Vol.33 (8), p.678-682

2011

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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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Clinical profiles for seizure remission and developmental gains after total corpus callosotomy

Brain & development (Tokyo. 1979), 2016-01, Vol.38 (1), p.47-53

2016

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Panax Ginseng: A Newly Identified Cause of Gynecomastia

The Tohoku Journal of Experimental Medicine, 2012, Vol.228(2), pp.143-145

2012

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Utility of Thallium-201 Scintigraphy in Tolosa-Hunt Syndrome

The Tohoku Journal of Experimental Medicine, 2013, Vol.229(1), pp.83-86

2013

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Clinical features and long-term outcome of a group of Japanese children with inflammatory central nervous system disorders and seropositivity to myelin-oligodendrocyte glycoprotein antibodies

Brain & development (Tokyo. 1979), 2015-10, Vol.37 (9), p.849-852

2015

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Characteristic findings of skeletal muscle MRI in caveolinopathies

Neuromuscular disorders : NMD, 2018-10, Vol.28 (10), p.857-862

2018

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Acute encephalitis with refractory, repetitive partial seizures: Pathological findings and a new therapeutic approach using tacrolimus

Brain & development (Tokyo. 1979), 2016-09, Vol.38 (8), p.772-776

2016

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Acute encephalopathy with a truncation mutation in the SCN1A gene: A case report

Epilepsia (Copenhagen), 2010-09, Vol.51 (9), p.1886-1888

2010

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Abdominal and lower back pain in pediatric idiopathic stabbing headache

Pediatrics (Evanston), 2014-01, Vol.133 (1), p.e245

2014

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Effect of a blackout in pediatric patients with home medical devices during the 2011 eastern Japan earthquake

Brain & development (Tokyo. 1979), 2014-02, Vol.36 (2), p.143-147

2014

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Dramatic response after functional hemispherectomy in a patient with epileptic encephalopathy carrying a de novo COL4A1 mutation

Brain & development (Tokyo. 1979), 2017-04, Vol.39 (4), p.337-340

2017

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A patient with a 6q22.1 deletion and a phenotype of non-progressive early-onset generalized epilepsy with tremor

Epilepsy & behavior reports, 2021-01, Vol.15, p.100405-100405, Article 100405

2021

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Pediatric-Onset Extracephalic Stabbing Pain

Journal of child neurology, 2014-08, Vol.29 (8), p.NP47-NP48

2014

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A case of 3p deletion syndrome associated with cerebellar hemangioblastoma

Brain & development (Tokyo. 1979), 2016-02, Vol.38 (2), p.257-260

2016

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Myoclonic axial jerks for diagnosing atypical evolution of ataxia telangiectasia

Brain & development (Tokyo. 1979), 2015-03, Vol.37 (3), p.362-365

2015

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Early replacement therapy in a first Japanese case with autosomal recessive guanosine triphosphate cyclohydrolase I deficiency with a novel point mutation

Brain & development (Tokyo. 1979), 2014-03, Vol.36 (3), p.268-271

2014

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Erythema nodosum as the initial symptom of Crohn's disease: A case report

De novo GABRA1 mutations in Ohtahara and West syndromes

Glabellar ecchymosis and headache: Variations of pain‐associated ecchymosis

Efficacy of long‐term adrenocorticotropic hormone therapy for West syndrome: A retrospective multicenter case series

Novel missense mutation in CLN8 in late infantile neuronal ceroid lipofuscinosis: The first report of a CLN8 mutation in Japan

Neuroepidemiology of Porencephaly, Schizencephaly, and Hydranencephaly in Miyagi Prefecture, Japan

Human Herpes Virus Type 6 Can Cause Skin Lesions at the BCG Inoculation Site Similar to Kawasaki Disease

Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy

A female case of West syndrome with remission of spasms following multiple cerebral hemorrhages

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

Clinical profiles for seizure remission and developmental gains after total corpus callosotomy

Panax Ginseng: A Newly Identified Cause of Gynecomastia

Utility of Thallium-201 Scintigraphy in Tolosa-Hunt Syndrome

Clinical features and long-term outcome of a group of Japanese children with inflammatory central nervous system disorders and seropositivity to myelin-oligodendrocyte glycoprotein antibodies

Characteristic findings of skeletal muscle MRI in caveolinopathies

Acute encephalitis with refractory, repetitive partial seizures: Pathological findings and a new therapeutic approach using tacrolimus

Acute encephalopathy with a truncation mutation in the SCN1A gene: A case report

Abdominal and lower back pain in pediatric idiopathic stabbing headache

Effect of a blackout in pediatric patients with home medical devices during the 2011 eastern Japan earthquake

Dramatic response after functional hemispherectomy in a patient with epileptic encephalopathy carrying a de novo COL4A1 mutation

A patient with a 6q22.1 deletion and a phenotype of non-progressive early-onset generalized epilepsy with tremor

Pediatric-Onset Extracephalic Stabbing Pain

A case of 3p deletion syndrome associated with cerebellar hemangioblastoma

Myoclonic axial jerks for diagnosing atypical evolution of ataxia telangiectasia

Early replacement therapy in a first Japanese case with autosomal recessive guanosine triphosphate cyclohydrolase I deficiency with a novel point mutation

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