Showing results (61-70 of 140) with videos related to

Sort By:
Pageof 14
Epilepsia|March 28, 2008
Alpha-[11C]methyl-L-tryptophan uptake in patients with periventricular nodular heterotopia and epilepsyJun Natsume, Neda Bernasconi, Yahya Aghakhani, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 31, 2017
Detecting sub-second changes in brain activation patterns during interictal epileptic spike using simultaneous EEG-fMRIEpifanio Bagarinao, Satoshi Maesawa, Yuji Ito, et al.
Brain & Development|March 24, 2020
Clinical findings in patients with febrile seizure after 5 years of age: A retrospective studyMotoko Ogino, Mitsuru Kashiwagi, Takuya Tanabe, et al.
Brain & Development|December 16, 2019
Novel biallelic FA2H mutations in a Japanese boy with fatty acid hydroxylase-associated neurodegenerationMasahiro Kawaguchi, Takayuki Sassa, Hiroyuki Kidokoro, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|October 4, 2016
Primary psoas abscess caused by group A streptococcus in a child: Case report with microbiologic findingsYasuko Kamiya, Tadao Hasegawa, Yasuhiko Takegami, et al.
Magnetic Resonance Imaging|March 15, 2021
Age estimates from brain magnetic resonance images of children younger than two years of age using deep learningMasahiro Kawaguchi, Hiroyuki Kidokoro, Rintaro Ito, et al.
Human Mutation|April 5, 2013
Mutations in the C-terminal domain of ColQ in endplate acetylcholinesterase deficiency compromise ColQ-MuSK interactionTomohiko Nakata, Mikako Ito, Yoshiteru Azuma, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|July 21, 2017
Magnetic resonance spectroscopy in preterm infants: association with neurodevelopmental outcomesReina Hyodo, Yoshiaki Sato, Miharu Ito, et al.
Brain & Development|December 4, 2020
The eldest case of MICPCH with CASK mutation exhibiting gross motor regressionYosuke Nishio, Hiroyuki Kidokoro, Toshiki Takeo, et al.
American Journal of Medical Genetics. Part A|January 25, 2014
A novel WTX mutation in a female patient with osteopathia striata with cranial sclerosis and hepatoblastomaAtsushi Fujita, Nobuhiko Ochi, Hidehiko Fujimaki, et al.
Pageof 14