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Brain & Development|July 2, 2015
The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorderSanem Yilmaz, Sarenur Gokben, Gul Serdaroglu, et al.Brain & Development|May 23, 2015
Phenytoin toxicity in two-month-old Thai infant with CYP2C9 gene polymorphism--A case reportMontida Veeravigrom, Vorapol Jaroonvanichkul, Wiracha Netbaramee, et al.Brain & Development|June 2, 2015
Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduriaYupeng Liu, Xiyuan Li, Qiao Wang, et al.Brain & Development|June 22, 2015
Late-onset epileptic spasms in a patient with 22q13.3 deletion syndromeNobutsune Ishikawa, Yoshiyuki Kobayashi, Yuji Fujii, et al.Brain & Development|January 1, 1982
Mortality and clinical features in cases of death among epileptic childrenT Kurokawa, K C Fung, T Hanai, et al.Brain & Development|January 1, 1982
Facial hemangioma with cerebrovascular anomalies and cerebellar hypoplasiaY Mizuno, T Kurokawa, Y Numaguchi, et al.Brain & Development|January 1, 1989
Polygraphic features of a victim of sudden infant death syndrome and of infants with apparent life-threatening eventJ Kohyama, Y IwakawaBrain & Development|January 1, 1989
Epidermal nevus syndrome with hemimegalencephaly: a clinical report of a case with acanthosis nigricans-like nevi on the face and neck, hemimegalencephaly, and hemihypertrophy of the bodyR Sakuta, H Aikawa, S Takashima, et al.Brain & Development|July 21, 2016
Elevated taurine and glutamate in cerebral juvenile xanthogranuloma on MR spectroscopyKen Matsubara, Harushi Mori, Nozomi Hirai, et al.Brain & Development|April 28, 2020
Variant in the neuronal vesicular SNARE VAMP2 (synaptobrevin-2): First report in JapanYasuo Sunaga, Kazuhiro Muramatsu, Kenjirou Kosaki, et al.Pageof 483