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Brain & Development|May 7, 2014
Episodic tremors representing cortical myoclonus are characteristic in Angelman syndrome due to UBE3A mutationsMasahide Goto, Yoshiaki Saito, Ryoko Honda, et al.Brain & Development|April 16, 2014
Study of epileptic drop attacks in symptomatic epilepsy of early childhood - differences from those in myoclonic-astatic epilepsyYasushi Itoh, Hirokazu Oguni, Yoshiko Hirano, et al.Brain & Development|April 17, 2014
Hypofibrinogenemia caused by adrenocorticotropic hormone for infantile spasms: a case reportAtsushi Kamei, Nami Araya, Manami Akasaka, et al.Brain & Development|May 3, 2014
Prognostic factors for acute encephalopathy with bright tree appearanceJunji Azuma, Shin Nabatame, Sayaka Nakano, et al.Brain & Development|April 22, 2008
Management of and prophylaxis against status epilepticus in children with severe myoclonic epilepsy in infancy (SMEI; Dravet syndrome)--a nationwide questionnaire survey in JapanTakuya Tanabe, Yutaka Awaya, Toyojiro Matsuishi, et al.Brain & Development|February 22, 2008
Serial brain imaging analysis of stroke-like episodes in MELASHiromichi Ito, Kenji Mori, Masafumi Harada, et al.Brain & Development|October 16, 2016
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrumSalvatore Grosso, Maria Alessandra Carluccio, Elena Cardaioli, et al.Brain & Development|November 9, 2016
Amelioration of intractable epilepsy by adjunct vagus nerve stimulation therapy in a girl with a CDKL5 mutationShimpei Baba, Yuji Sugawara, Kengo Moriyama, et al.Brain & Development|January 1, 1989
Type II fiber myolysis in a patient with hypocarnitinemiaS Kimura, S MiyakeBrain & Development|February 11, 2014
Adrenal insufficiency in a child with MELAS syndromeBushra Afroze, Nida Amjad, Shahnaz H Ibrahim, et al.Pageof 483