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Brain & Development|August 28, 2016
Cerebral arteriopathy associated with heterozygous Arg179Cys mutation in the ACTA2 gene: Report in 2 newborn siblingsJose de Grazia, Ignacio Delgado, Angel Sanchez-Montanez, et al.Brain & Development|May 11, 2017
Structural brain network analysis of children with localization-related epilepsyKanako Takeda, Hiroshi Matsuda, Yusaku Miyamoto, et al.Brain & Development|May 22, 2017
Neuroimaging and neuropathological characteristics of cerebellar injury in extremely low birth weight infantsMayumi Matsufuji, Nozomi Sano, Hisashi Tsuru, et al.Brain & Development|July 6, 2017
Spinal muscular atrophy carriers with two SMN1 copiesMawaddah Ar Rochmah, Hiroyuki Awano, Tomonari Awaya, et al.Brain & Development|September 4, 2016
Reversible splenial lesion syndrome in children: Retrospective study and summary of case seriesWen-Xiong Chen, Hong-Sheng Liu, Si-Da Yang, et al.Brain & Development|January 12, 2010
Migraine in junior high-school students: A prospective 3-academic-year cohort studyAnannit Visudtibhan, Lunliya Thampratankul, Chaiyos Khongkhatithum, et al.Brain & Development|January 12, 2010
Seizures and EEG pattern in Kabuki syndromeMonica Lodi, Rosanna Chifari, Cecilia Parazzini, et al.Brain & Development|December 22, 2009
Bilateral occipital cortical dysplasia and white matter T2 hyperintensity with mild non-specific myopathy: two sibling casesTohru Okanishi, Tatsuya Ishikawa, Satoru Kobayashi, et al.Brain & Development|February 5, 2010
Two novel missense mutations in the aspartoacylase gene in a Chinese patient with congenital Canavan diseaseHuiwen Zhang, Xiaoqin Liu, Xuefan GuPageof 482