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Brain & Development|November 16, 2016
Hyperekplexia: Report on phenotype and genotype of 16 Jordanian patientsAmira Masri, Seo-Kyung Chung, Mark I ReesBrain & Development|October 5, 2016
Neurodevelopmental outcome of term infants with perinatal asphyxia with hypoxic ischemic encephalopathy stage IISudhir Adhikari, Kalipatnam Seshagiri RaoBrain & Development|October 5, 2016
Early cardiac involvement in an infantile Sandhoff disease case with novel mutationsHsiu-Fen Lee, Ching-Shiang Chi, Chi-Ren TsaiBrain & Development|October 30, 2016
A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus-Merzbacher disease: A new MRI findingEfterpi Pavlidou, Vijaya Ramachandran, Veronica Govender, et al.Brain & Development|December 8, 2016
Total corpus callosotomy for epileptic spasms after acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) in a case with tuberous sclerosis complexTohru Okanishi, Ayataka Fujimoto, Hirotaka Motoi, et al.Brain & Development|December 9, 2016
Novel mutation in a patient with late onset GLUT1 deficiency syndromeSandra Juozapaite, Ruta Praninskiene, Birute Burnyte, et al.Brain & Development|January 30, 2008
New neurocutaneous syndrome with defect in cell trafficking and melanosome pathway: the future challengeRaffaella Zannolli, Sabrina Buoni, Margherita de Santi, et al.Brain & Development|February 26, 2008
The corticospinal tract in Sturge-Weber syndrome: a diffusion tensor tractography studyLalitha Sivaswamy, Kumar Rajamani, Csaba Juhasz, et al.Brain & Development|February 12, 2008
Frontal behavioral syndromes in Prader-Willi syndromeKaeko Ogura, Mayumi Shinohara, Kousaku Ohno, et al.Brain & Development|March 11, 2008
Hyperoxic exposure leads to cell death in the developing brainUluç Yiş, Semra Hiz Kurul, Abdullah Kumral, et al.Pageof 483