BRAIN & DEVELOPMENT

Neuronal ceroid lipofuscinosis type-11 in an adolescent

Ketogenic diet as a successful early treatment modality for SCN2A mutation

Phenotypic manifestations between male and female children with CDKL5 mutations

Age-related differences in frontal lobe function in children with ADHD

Clinical manifestations, treatment outcomes, and prognostic factors of pediatric anti-NMDAR encephalitis in tertiary care hospitals: A multicenter retrospective/prospective cohort study

Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case report

Prediction of poor neurological development in patients with symptomatic congenital cytomegalovirus diseases after oral valganciclovir treatment

Abnormal cortical activation during silent reading in adolescents with autism spectrum disorder

Early enzyme replacement therapy enables a successful hematopoietic stem cell transplantation in mucopolysaccharidosis type IH: Divergent clinical outcomes in two Japanese siblings

Epilepsy in patients with EAST syndrome caused by mutation in the KCNJ10

Nutritional status among women whose pregnancy outcome was afflicted with neural tube defects in Tigray region of Ethiopia

Novel method using Hjorth mobility analysis for diagnosing attention-deficit hyperactivity disorder in girls

Serum carnitine levels of children with epilepsy: Related factors including valproate

Brain gliomas, hydrocephalus and idiopathic aqueduct stenosis in children with neurofibromatosis type 1

A case of subacute combined degeneration of the spinal cord due to folic acid and copper deficiency

Coexistence of a CAV3 mutation and a DMD deletion in a family with complex muscular diseases

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

Facial nerve palsy associated with atomoxetine-induced hypertension

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

Association of inattention with slow-spindle density in sleep EEG of children with attention deficit-hyperactivity disorder

Anterior cingulate cortex involvement in non-paraneoplastic limbic encephalitis

A 16q22.2-q23.1 deletion identified in a male infant with West syndrome

Three Japanese patients with 3p13 microdeletions involving FOXP1

Incidence of infantile spinal muscular atrophy on Shikoku Island of Japan

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

Age related signal changes of the pituitary stalk on thin-slice magnetic resonance imaging in infants

Neuropsychological outcomes of childhood acute necrotizing encephalopathy

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

Disrupted cortico-ponto-cerebellar pathway in patients with hemimegalencephaly

Phenotypic features of 1q41q42 microdeletion including WDR26 and FBXO28 are clinically recognizable: The first case from Japan

Motor and cognitive development of children with Down syndrome: The effect of acquisition of walking skills on their cognitive and language abilities

Perampanel attenuates myoclonus in a patient with neuronal ceroid lipofuscinoses type 2 disease

Findings of amplitude-integrated electroencephalogram recordings and serum vitamin B6 metabolites in perinatal lethal hypophosphatasia during enzyme replacement therapy

Sensory processing in children with autism spectrum disorder and the mental health of primary caregivers

Fulminant cerebral venous thrombosis associated with the m.3243A>G MELAS mutation: A new guise for an old disease

Predicting the outcomes of targeted temperature management for children with seizures and/or impaired consciousness accompanied by fever without known etiology

Event-related potentials and behavior performance scores in children with sleep-disordered breathing

Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome

Oxidant and antioxidant levels and DNA damage in tuberous sclerosis

A severe case of Menkes disease with repeated bone fracture during the neonatal period, followed by multiple arterial occlusion

Usefulness of diagnostic tools in a GLUT1 deficiency syndrome patient with 2 inherited mutations

Detailed clinical course of fatal acute encephalopathy in children

Central nervous system vasculitis from Epstein-Barr virus-associated T/natural killer-cell lymphoproliferative disorder in children: A case report

Single-fiber electromyography-based diagnosis of CACNA1A mutation in children: A potential role of the electrodiagnosis in the era of whole exome sequencing

Successful corpus callosotomy for post-encephalopathic refractory epilepsy in a patient with MECP2 duplication syndrome

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

Automatic calculation of Mercuri grades from CT and MR muscle images