Brain and Development (ISSN 0387-7604) is the Official Journal of the Japanese Society of Child Neurology, and is aimed to promote clinical child neurology and developmental neuroscience.The journal is devoted to publishing Review Articles, Full Length Original Papers, Case Reports and Letters to the Editor in the field of Child Neurology and related sciences. Proceedings of meetings, and professional announcements will be published at the Editor's discretion. Letters concerning articles published in Brain and Development and other relevant issues are also welcome.
《脑与发育》（ISSN 0387-7604）是日本儿童神经病学学会的官方期刊，旨在促进临床儿童神经病学和发育神经科学的发展。该期刊致力于发表儿童神经病学和相关科学领域的综述文章、全文原始论文、病例报告和致编辑的信件。会议记录和专业公告将由编辑酌情发表。也欢迎有关在《大脑与发育》和其他相关问题上发表的文章的来信。
Clinical and neurodevelopmental features in children with cerebral palsy and probable congenital Zika
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.03.005
Treatment options in pediatric super-refractory status epilepticus
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.11.011
MicroRNA-31 regulating apoptosis by mediating the phosphatidylinositol-3 kinase/protein kinase B signaling pathway in treatment of spinal cord injury
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.04.010
Neuronal ceroid lipofuscinosis type-11 in an adolescent
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.03.004
Ketogenic diet as a successful early treatment modality for SCN2A mutation
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.10.015
Phenotypic manifestations between male and female children with CDKL5 mutations
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.05.003
Age-related differences in frontal lobe function in children with ADHD
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.03.006
Clinical manifestations, treatment outcomes, and prognostic factors of pediatric anti-NMDAR encephalitis in tertiary care hospitals: A multicenter retrospective/prospective cohort study
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.12.009
Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.04.002
Prediction of poor neurological development in patients with symptomatic congenital cytomegalovirus diseases after oral valganciclovir treatment
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.04.016
Abnormal cortical activation during silent reading in adolescents with autism spectrum disorder
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.10.013
Early enzyme replacement therapy enables a successful hematopoietic stem cell transplantation in mucopolysaccharidosis type IH: Divergent clinical outcomes in two Japanese siblings
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.01.008
Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.03.009
Nutritional status among women whose pregnancy outcome was afflicted with neural tube defects in Tigray region of Ethiopia
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.12.005
Novel method using Hjorth mobility analysis for diagnosing attention-deficit hyperactivity disorder in girls
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.11.006
Serum carnitine levels of children with epilepsy: Related factors including valproate
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.02.010
Brain gliomas, hydrocephalus and idiopathic aqueduct stenosis in children with neurofibromatosis type 1
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.04.003
A case of subacute combined degeneration of the spinal cord due to folic acid and copper deficiency
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.07.006
Coexistence of a CAV3 mutation and a DMD deletion in a family with complex muscular diseases
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.01.005
Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.06.004
Facial nerve palsy associated with atomoxetine-induced hypertension
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.09.009
Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.07.008
Association of inattention with slow-spindle density in sleep EEG of children with attention deficit-hyperactivity disorder
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.05.004
Anterior cingulate cortex involvement in non-paraneoplastic limbic encephalitis
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.04.006
A 16q22.2-q23.1 deletion identified in a male infant with West syndrome
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.07.005
Three Japanese patients with 3p13 microdeletions involving FOXP1
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.10.016
Incidence of infantile spinal muscular atrophy on Shikoku Island of Japan
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.07.016
Gender differences in occurrence of behavioral and emotional problems at the lower grades of elementary school: Association with developmental and behavioral characteristics at 5\u202fyears
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.06.001
Age related signal changes of the pituitary stalk on thin-slice magnetic resonance imaging in infants
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.11.009
Neuropsychological outcomes of childhood acute necrotizing encephalopathy
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.07.007
High incidence of status epilepticus and ongoing seizures on arrival to the hospital due to high prevalence of febrile seizures in Izumo, Japan: A questionnaire-based study
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.07.009
Disrupted cortico-ponto-cerebellar pathway in patients with hemimegalencephaly
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.01.002
Phenotypic features of 1q41q42 microdeletion including WDR26 and FBXO28 are clinically recognizable: The first case from Japan
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.12.006
Motor and cognitive development of children with Down syndrome: The effect of acquisition of walking skills on their cognitive and language abilities
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.11.008
Perampanel attenuates myoclonus in a patient with neuronal ceroid lipofuscinoses type 2 disease
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.05.001
Findings of amplitude-integrated electroencephalogram recordings and serum vitamin B6 metabolites in perinatal lethal hypophosphatasia during enzyme replacement therapy
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.03.015
Sensory processing in children with autism spectrum disorder and the mental health of primary caregivers
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.11.005
Fulminant cerebral venous thrombosis associated with the m.3243A>G MELAS mutation: A new guise for an old disease
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.07.002
Predicting the outcomes of targeted temperature management for children with seizures and/or impaired consciousness accompanied by fever without known etiology
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.03.007
Event-related potentials and behavior performance scores in children with sleep-disordered breathing
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.04.008
Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.03.003
Oxidant and antioxidant levels and DNA damage in tuberous sclerosis
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.10.014
A severe case of Menkes disease with repeated bone fracture during the neonatal period, followed by multiple arterial occlusion
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.06.005
Usefulness of diagnostic tools in a GLUT1 deficiency syndrome patient with 2 inherited mutations
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.05.008
Detailed clinical course of fatal acute encephalopathy in children
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.04.012
Central nervous system vasculitis from Epstein-Barr virus-associated T/natural killer-cell lymphoproliferative disorder in children: A case report
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.05.009
Single-fiber electromyography-based diagnosis of CACNA1A mutation in children: A potential role of the electrodiagnosis in the era of whole exome sequencing
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.06.006
Successful corpus callosotomy for post-encephalopathic refractory epilepsy in a patient with MECP2 duplication syndrome
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2018.09.008
Activation of leukocyte immunoglobulin-like receptor B2 signaling pathway in cortical lesions of pediatric patients with focal cortical dysplasia type IIb and tuberous sclerosis complex
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.08.002
Automatic calculation of Mercuri grades from CT and MR muscle images
来源期刊：Brain and DevelopmentDOI：10.1016/j.braindev.2019.06.008
