| Clinical and neurodevelopmental features in children with cerebral palsy and probable congenital Zika |
12 |
| The course of awake breathing disturbances across the lifespan in Rett syndrome |
11 |
| Everolimus for epilepsy and autism spectrum disorder in tuberous sclerosis complex: EXIST-3 substudy in Japan |
11 |
| Migraine and associated comorbidities are three times more frequent in children with ADHD and their mothers |
9 |
| Differential effects on sodium current impairments by distinct &ITSCN1A&IT mutations in GABAergic neurons derived from Dravet syndrome patients |
9 |
| Recreational nitrous oxide abuse related subacute combined degeneration of the spinal cord in adolescents - A case series and literature review |
9 |
| Serial MRI findings of acute flaccid myelitis during an outbreak of enterovirus D68 infection in Japan |
8 |
| Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations |
8 |
| Robot-assisted training using Hybrid Assistive Limb (R) for cerebral palsy |
8 |
| Neonatal seizures and white matter injury: Role of rotavirus infection and probiotics |
7 |
| Efficacy of CBD-enriched medical cannabis for treatment of refractory epilepsy in children and adolescents - An observational, longitudinal study |
7 |
| Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders |
7 |
| Anti-N-methyl-D-aspartate receptor encephalitis in children: Incidence and experience in Hong Kong |
7 |
| A novel mutation in sphingosine-1-phosphate lyase causing congenital brain malformation |
7 |
| An infant case of diffuse cerebrospinal lesions and cardiomyopathy caused by a BOLA3 mutation |
7 |
| ATP1A3-related epileptic encephalopathy responding to ketogenic diet |
7 |
| The ketogenic diet for super-refractory status epilepticus patients in intensive care units |
7 |
| MicroRNA-31 regulating apoptosis by mediating the phosphatidylinositol-3 kinase/protein kinase B signaling pathway in treatment of spinal cord injury |
6 |
| Treatment options in pediatric super-refractory status epilepticus |
6 |
| Incidence and characteristics of norovirus-associated benign convulsions with mild gastroenteritis, in comparison with rotavirus ones |
6 |
| SCN2A mutation in an infant presenting with migrating focal seizures and infantile spasm responsive to a ketogenic diet |
6 |
| Correlation between human nervous system development and acquisition of fetal skills: An overview |
5 |
| Long-term home non-invasive positive pressure ventilation in children: Results from a single center in Japan |
5 |
| Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations |
5 |
| Behavioral profiles in Rett syndrome: Data from the natural history study |
5 |
| Genetic analysis of undiagnosed ataxia-telangiectasia-like disorders |
5 |
| Clinical time course of pediatric acute disseminated encephalomyelitis |
5 |
| Neuronal ceroid lipofuscinosis type-11 in an adolescent |
5 |
| Ketogenic diet as a successful early treatment modality for SCN2A mutation |
5 |
| Diagnostic challenge for the rare lysosomal storage disease: Late infantile GM1 gangliosidosis |
5 |
| De novo HDAC8 mutation causes Rett-related disorder with distinctive facial features and multiple congenital anomalies |
5 |
| Novel &ITBICD2 &ITmutation in a Japanese family with autosomal dominant lower extremity-predominant spinal muscular atrophy-2 |
4 |
| GRIN2A mutations in epilepsy-aphasia spectrum disorders |
4 |
| Prediction of poor neurological development in patients with symptomatic congenital cytomegalovirus diseases after oral valganciclovir treatment |
4 |
| A quinidine non responsive novel KCNT1 mutation in an Indian infant with epilepsy of infancy with migrating focal seizures |
4 |
| Serum carnitine levels of children with epilepsy: Related factors including valproate |
4 |
| Rhinovirus-associated acute encephalitis/encephalopathy and cerebellitis |
4 |
| A novel ZC4H2 gene mutation, K209N, in Japanese siblings with arthrogryposis multiplex congenita and intellectual disability: characterization of the K209N mutation and clinical findings |
4 |
| Successful treatment of normokalemic periodic paralysis with hydrochlorothiazide |
4 |
| CACNAIA-related early-onset encephalopathy with myoclonic epilepsy: A case report |
4 |
| Treatment of infantile spasms by pediatric neurologists in Japan |
4 |
| Infantile-onset spinocerebellar ataxia type 5 associated with a novel SPTBN2 mutation: A case report |
4 |
| Neurodevelopmental disorders in children with macrocephaly: A prevalence study and PTEN gene |
4 |
| A novel germline PIGA mutation causes early-onset epileptic encephalopathies in Chinese monozygotic twins |
4 |
| Rituximab was effective for acute disseminated encephalomyelitis followed by recurrent optic neuritis with anti-myelin oligodendrocyte glycoprotein antibodies |
4 |
| Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutation |
4 |
| Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2 |
3 |
| Spike persistence and normalization in benign epilepsy with centrotemporal spikes - Implications for management |
3 |
| MECP2 mutation in a boy with severe apnea and sick sinus syndrome |
3 |
| Age-related differences in frontal lobe function in children with ADHD |
3 |
