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Brain & Development|November 17, 2020
Neuroimaging manifestations and genetic heterogeneity of Walker-Warburg syndrome in Saudi patientsSara Alharbi, Amal Alhashem, Fowzan Alkuraya, et al.Brain & Development|January 1, 1987
Maternal alcohol ingestion and neural tube defects: observation of four brothers in a familyM Castro-Gago, I Novo, J PeñaBrain & Development|January 11, 2023
Skeletal anomaly and opisthotonus in early-onset epileptic encephalopathy with KCNQ2 abnormalityOsamu Kawano, Takashi Saito, Noriko Sumitomo, et al.Brain & Development|January 7, 2021
Thyroid crisis mimicking clinically mild encephalitis/encephalopathy with a reversible splenial lesion: A pediatric case reportKohei Matsubara, Ichiro Kuki, Naohiro Yamamoto, et al.Brain & Development|January 9, 2021
Variance in the pathophysiological impact of the hemizygosity of gamma-aminobutyric acid type A receptor subunit genes between Prader-Willi syndrome and Angelman syndromeKiyoshi Egawa, Shinji Saitoh, Naoko Asahina, et al.Brain & Development|June 1, 2021
Recurrent acute necrotizing encephalopathy in a boy with RANBP2 mutation and thermolabile CPT2 variant: The first case of ANE1 in JapanEri Ohashi, Itaru Hayakawa, Yuka Murofushi, et al.Brain & Development|June 2, 2021
Nonconvulsive status epilepticus following rotavirus gastroenteritis in two pediatric patientsKo Hirata, Yuji Sugawara, Ai Hoshino, et al.Brain & Development|January 12, 2021
Biallelic XPR1 mutation associated with primary familial brain calcification presenting as paroxysmal kinesigenic dyskinesia with infantile convulsionsLi-Ou Tang, Bing-Hui Hou, Xiao-Na Zhang, et al.Brain & Development|June 7, 2021
Two cases of DYNC1H1 mutations with intractable epilepsyAyumi Matsumoto, Karin Kojima, Fuyuki Miya, et al.Brain & Development|January 1, 1988
Developmental changes of pattern reversal visual evoked potentialsK Aso, K Watanabe, T Negoro, et al.Pageof 483