Brain and Development Journal

Is hiragana decoding impaired in children with periventricular leukomalacia?

Fulltext Access 7 Pages 2018

Genotypes and phenotypes in 20 Chinese patients with type 2 Gaucher disease

Fulltext Access 8 Pages 2018

Fosphenytoin vs. continuous midazolam for pediatric febrile status epilepticus

Fulltext Access 7 Pages 2018

Incidence of childhood epilepsy: A population-based study in rural Japan

Fulltext Access 5 Pages 2018

Investigation of neuronal auto-antibodies in children diagnosed with epileptic encephalopathy of unknown cause

Fulltext Access 9 Pages 2018

Urinary prostaglandin metabolites as Duchenne muscular dystrophy progression markers

Fulltext Access 8 Pages 2018

Loss of myelinated axons and astrocytosis in an autopsy case of acute encephalopathy with biphasic seizures and late reduced diffusion

Fulltext Access 5 Pages 2018

Radiotherapy for Langerhans cell histiocytosis with paraplegia: A rare oncologic emergency case report in infancy and literature review

Fulltext Access 4 Pages 2018

Quantitative evaluation of regional cerebral blood flow changes during childhood using 123I-N-isopropyl-iodoamphetamine single-photon emission computed tomography

Fulltext Access 9 Pages 2018

Migraine and associated comorbidities are three times more frequent in children with ADHD and their mothers

Fulltext Access 8 Pages 2018

Nonketotic hyperglycinemia: Clinical range and outcome of a rare neurometabolic disease in a single-center

Fulltext Access 11 Pages 2018

Infantile spasms in a mosaic monocentric and duplicated SMC 15 patient

Fulltext Access 6 Pages 2018

A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features

Fulltext Access 5 Pages 2018

Novel IARS2 mutations in Japanese siblings with CAGSSS, Leigh, and West syndrome

Fulltext Access 5 Pages 2018

Two cases of childhood narcolepsy mimicking epileptic seizures in video-EEG/EMG

Fulltext Access 4 Pages 2018

Anti-MOG antibody encephalitis mimicking neurological deterioration in a case of Rett syndrome with MECP2 mutation

Fulltext Access 4 Pages 2018