Showing results (2731-2740 of 4,780) with videos related to
Sort By:
Pageof 478
Brain & Development|July 25, 2018
Cyclic alternating pattern in infants with congenital hypothyroidismRafael Santana-Miranda, Chiharu Murata, Oliveiro Bruni, et al.Brain & Development|August 7, 2018
Atypical PEX16 peroxisome biogenesis disorder with mild biochemical disruptions and long survivalNuha Al Zaabi, Anoud Kendi, Fatma Al-Jasmi, et al.Brain & Development|May 15, 2017
Electrical status epilepticus during sleep in Mowat-Wilson syndromePaolo Bonanni, Susanna Negrin, Anna Volzone, et al.Brain & Development|January 1, 1988
Defects in muscle fiber growth in fatal infantile cytochrome c oxidase deficiencyI Nonaka, Y Koga, E Okino, et al.Brain & Development|May 27, 2018
Association of developing childhood epilepsy subsequent to febrile seizure: A population-based cohort studyLin-Mei Chiang, Go-Shine Huang, Chi-Chin Sun, et al.Brain & Development|September 4, 2016
RANBP2 mutation in an Indian child with recurrent acute necrotizing encephalopathyVishal Sondhi, Biswaroop Chakrabarty, Atin Kumar, et al.Brain & Development|September 4, 2016
Efficacy of bezafibrate on fibroblasts of glutaric acidemia type II patients evaluated using an in vitro probe acylcarnitine assayKenji Yamada, Hironori Kobayashi, Ryosuke Bo, et al.Brain & Development|September 6, 2016
Hippocampal signal abnormality on the first day of illness in acute encephalopathy with biphasic seizures and late reduced diffusion caused by HHV-6 infectionTakuya Matsuda, Shuichi Shimakawa, Hiromitsu Toshikawa, et al.Brain & Development|September 1, 2016
Quinidine therapy for West syndrome with KCNTI mutation: A case reportMasataka Fukuoka, Ichiro Kuki, Hisashi Kawawaki, et al.Brain & Development|August 22, 2016
Two mild cases of Dravet syndrome with truncating mutation of SCN1AToru Takaori, Akira Kumakura, Atsushi Ishii, et al.Pageof 478