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Brain & Development|March 4, 2022
Lacosamide monotherapy for the treatment of childhood epilepsy with centrotemporal spikesTohru Okanishi, Yuji Fujii, Satoru Sakuma, et al.Brain & Development|August 14, 2018
Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcificationChang-He Shi, Shuo Zhang, Zhi-Hua Yang, et al.Brain & Development|July 26, 2018
Novel IARS2 mutations in Japanese siblings with CAGSSS, Leigh, and West syndromeYusuke Takezawa, Hiromi Fujie, Atsuo Kikuchi, et al.Brain & Development|June 5, 2018
Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutationsPauline Marzin, Cyril Mignot, Nathalie Dorison, et al.Brain & Development|May 27, 2018
Neurodevelopmental outcomes in children with prenatally diagnosed corpus callosal abnormalitiesHye-Ryun Yeh, Hyo-Kyoung Park, Hyun-Jin Kim, et al.Brain & Development|May 5, 2018
Spontaneous movements of preterm infants is associated with outcome of gross motor developmentSaori Miyagishima, Tadayoshi Asaka, Kaori Kamatsuka, et al.Brain & Development|December 22, 1999
Sleep abnormalities in mentally retarded autistic subjects: Down's syndrome with mental retardation and normal subjectsM Diomedi, P Curatolo, A Scalise, et al.Brain & Development|December 22, 1999
Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boyK Suwa, T Yamagata, M Y Momoi, et al.Brain & Development|March 21, 2000
Head stability during whole body movements in spastic diplegiaB Dan, E Bouillot, A Bengoetxea, et al.Brain & Development|March 21, 2000
Plasmapheresis in a child affected by acute disseminated encephalomyelitisP Balestri, S Grosso, A Acquaviva, et al.Pageof 483