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Brain & Development|February 24, 2019
Two unrelated girls with intellectual disability associated with a truncating mutation in the PPM1D penultimate exonYukiko Kuroda, Hiroaki Murakami, Takayuki Yokoi, et al.
Brain & Development|November 19, 2018
MRI findings in pediatric neuromyelitis optica spectrum disorder with MOG antibody: Four cases and review of the literatureAzusa Ikeda, Yoshihiro Watanabe, Hikari Kaba, et al.
Brain & Development|November 19, 2018
Abnormal cortical activation during silent reading in adolescents with autism spectrum disorderRei Ogawa, Kuriko Kagitani-Shimono, Junko Matsuzaki, et al.
Brain & Development|March 7, 2019
Is the motor skills checklist appropriate for assessing children in Japan?Yosuke Kita, Fumiko Ashizawa, Masumi Inagaki
Brain & Development|March 9, 2019
Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutationChihiro Matsumoto, Madoka Mori-Yoshimura, Satoru Noguchi, et al.
Brain & Development|January 24, 2021
Focal status and acute encephalopathy in a 13-year-old boy with de novo DNM1L mutation: Video-polygraphic pattern and clues for differential diagnosisMaria Margherita Mancardi, Claudia Nesti, Francesca Febbo, et al.
Brain & Development|February 16, 2021
Reliability and validity of the Japanese version of the Behavior Problem Inventory-Short FormMasahiko Inoue, Naoko Inada, Yoichi Gomi, et al.
Brain & Development|February 17, 2017
Cognitive and behavioral effects of new antiepileptic drugs in pediatric epilepsyRomina Moavero, Marta Elena Santarone, Cinzia Galasso, et al.
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