Satoru Ikemoto

Heterozygous Mutations in OAS1 Cause Infantile-Onset Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia

Kazutoshi Cho, Masafumi Yamada, Kazunaga Agematsu et al. · The American Journal of Human Genetics · 2018 · 36 citations · Full text

Genetics, Pulmonary Alveolar Proteinosis, Pathology +6

Biallelic loss‐of‐function <i>UBA5</i> mutations in a patient with intractable West syndrome and profound failure to thrive

Atsuro Daida, Shin‐ichiro Hamano, Satoru Ikemoto et al. · Epileptic Disorders · 2018 · 26 citations · Full text

Treatment of infantile spasms by pediatric neurologists in Japan

Shin‐ichiro Hamano, Toshisaburo Nagai, Ryuki Matsuura et al. · Brain and Development · 2018 · 25 citations

Pediatric Hydrocephalus, Pediatric Neurosurgery, Pediatrics +5

Phenotype–genotype correlations in patients with GNB1 gene variants, including the first three reported Japanese patients to exhibit spastic diplegia, dyskinetic quadriplegia, and infantile spasms

Wakaba Endo, Satoru Ikemoto, Noriko Togashi et al. · Brain and Development · 2019 · 23 citations

Phenotype–genotype Correlations, Genetic Disorder, Genetics +12

Efficacy and serum concentrations of perampanel for treatment of drug-resistant epilepsy in children, adolescents, and young adults: comparison of patients younger and older than 12 years

Satoru Ikemoto, Shin‐ichiro Hamano, Yuko Hirata et al. · Seizure · 2019 · 19 citations

Drug Safety, Young Adults, Drug-resistant Epilepsy +7