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Brain & Development|September 26, 2021
The first pediatric case of mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) associated with Neisseria meningitidisGizem Guner Ozenen, Zumrut Sahbudak Bal, Irem Ersayoglu, et al.
Brain & Development|September 26, 2021
Association of O blood type with the prognosis of acute necrotizing encephalopathy in childhood: A single-center cohort studyYeqing Wang, Suyun Qian, Kenchun Li, et al.
Brain & Development|February 5, 2022
The effectiveness of intravenous benzodiazepine for status epilepticus in Dravet syndromeKenjiro Kikuchi, Shin-Ichiro Hamano, Ryuki Matsuura, et al.
Brain & Development|January 29, 2022
Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegiaAkif Ayaz, Tugce Aksu Uzunhan, Kursad Aydin
Brain & Development|April 23, 2022
Early maladaptive schemas differing according to sex may contribute to migraine among the youthGülen Güler Aksu, Ozan Kayar, Ali Evren Tufan, et al.
Brain & Development|April 26, 2022
Cerebral white matter abnormalities associated with chromosome 18q duplicationJiayin Huang, Christine Saint-Martin, Guergana Tchakarska, et al.
Brain & Development|April 24, 2022
De novo POLR2A p.(Ile457Thr) variant associated with early-onset encephalopathy and cerebellar atrophy: expanding the phenotypic spectrumThea Giacomini, Marcello Scala, Giulia Nobile, et al.
Brain & Development|April 13, 2022
Paroxysmal limb dystonias associated with GABBR2 pathogenic variant: A case-based literature reviewGianluca D'Onofrio, Antonella Riva, Gabriella Di Rosa, et al.
Brain & Development|September 10, 2018
Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutationMona Entezam, Masoumeh Razipour, Saeed Talebi, et al.
Brain & Development|September 1, 2018
Rufinamide efficacy and safety in children aged 1-4 years with Lennox-Gastaut syndromeShin Hye Kim, Hoon-Chul Kang, Joon Soo Lee, et al.
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