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Brain & Development|February 1, 2020
A case of congenital herpes simplex virus infection diagnosed at 8 months of ageShiho Yamamoto, Tsunehisa Nagamori, Shigetsuna Komatsu, et al.Brain & Development|July 17, 2021
Neurodegeneration with brain iron accumulation: Characterization of clinical, radiological, and genetic features of pediatric patients from Southern IndiaNaveen Kumar Bhardwaj, Vykuntaraju K Gowda, Jitendra Saini, et al.Brain & Development|December 21, 2020
Refractory cerebral infarction in a child with an ACTA2 mutationKeita Kanamori, Yuri Sakaguchi, Kyoji Tsuda, et al.Brain & Development|July 5, 2022
The Japanese version of the children's sleep habits questionnaire (CSHQ-J): A validation study and influencing factorsRyuta Ishii, Hitoshi Obara, Shinichiro Nagamitsu, et al.Brain & Development|December 25, 2022
Perampanel therapy for intractable GRIN2D-related developmental and epileptic encephalopathy: A case report and literature reviewJiaqing Li, Yalan Zhou, Tangfeng Su, et al.Brain & Development|December 18, 2022
Two differential cavities in syringomyelia of pediatric Chiari I malformation presenting with unilateral foot dropNaoya Higuchi, Takuji Nakamura, Fumitaka Yoshioka, et al.Brain & Development|June 6, 2022
Late relapse of anti-N-methyl-d-aspartate receptor encephalitis with amusia and transiently reduced uptake in 123I-iomazenil single-photon emission computed tomographyNaoki Yamada, Ichiro Kuki, Taeka Hattori, et al.Brain & Development|June 21, 2022
The most severe form of LMNA-associated congenital muscular dystrophyYuka Murofushi, Itaru Hayakawa, Yuichi Abe, et al.Brain & Development|November 29, 2022
A novel variant in NEUROD2 in a patient with Rett-like phenotype points to Glu130 codon as a mutational hotspotDavide Politano, Simone Gana, Elena Pezzotti, et al.Pageof 482