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Brain & Development|March 1, 2016
Outcome of ketogenic diets in GLUT1 deficiency syndrome in Japan: A nationwide surveyTatsuya Fujii, Yasushi Ito, Satoru Takahashi, et al.Brain & Development|March 1, 2016
Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutationKatharina Sell, Katja Storch, Gabriele Hahn, et al.Brain & Development|March 2, 2016
Plasma exchange in pediatric anti-NMDAR encephalitis: A systematic reviewAgnese Suppiej, Margherita Nosadini, Luigi Zuliani, et al.Brain & Development|January 1, 1989
The changing panorama of infantile hydrocephalus and cerebral palsy over forty years--a Swedish surveyB Hagberg, G HagbergBrain & Development|February 25, 2016
Potential risk factors for dexmedetomidine withdrawal seizures in infants after surgery for congenital heart diseaseYoshihiro Takahashi, Kentaro Ueno, Yumiko Ninomiya, et al.Brain & Development|September 30, 2015
Three cases of right frontal megalencephaly: Clinical characteristics and long-term outcomeYoichi Ono, Yoshiaki Saito, Yoshihiro Maegaki, et al.Brain & Development|August 12, 2015
Chemical chaperone treatment for galactosialidosis: Effect of NOEV on β-galactosidase activities in fibroblastsMohammad Arif Hossain, Katsumi Higaki, Michiko Shinpo, et al.Brain & Development|August 26, 2015
Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophyJuan Ding, Dandan Zhao, Renqian Du, et al.Brain & Development|December 3, 2014
Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34Masakazu Mimaki, Takashi Shiihara, Mio Watanabe, et al.Brain & Development|January 1, 1989
Intraepidermal morphologic manifestations in lysosomal diseasesU Kaesgen, H H GoebelPageof 482