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Brain & Development|December 6, 2014
ACTH therapy on intractable epilepsy in Hemiconvulsion-Hemiplegia-Epilepsy syndromeShuichi Shimakawa, Shohei Nomura, Motoko Ogino, et al.Brain & Development|December 31, 2014
Carnitine deficiency: Risk factors and incidence in children with epilepsyMitsumasa Fukuda, Mika Kawabe, Makoto Takehara, et al.Brain & Development|August 24, 2014
Diffusion-weighted MRI for early diagnosis of neonatal herpes simplex encephalitisTohru Okanishi, Hiroyuki Yamamoto, Takatoshi Hosokawa, et al.Brain & Development|August 24, 2014
Efficacy of long term weekly ACTH therapy for intractable epilepsyTakehiko Inui, Tomoko Kobayashi, Satoru Kobayashi, et al.Brain & Development|June 9, 2012
Electrophysiological study of face inversion effects in Williams syndromeMiho Nakamura, Shoko Watanabe, Masumi Inagaki, et al.Brain & Development|June 9, 2012
Neuropathology of leukoencephalopathy with brainstem and spinal cord involvement and high lactate caused by a homozygous mutation of DARS2Sumimasa Yamashita, Noriko Miyake, Naomichi Matsumoto, et al.Brain & Development|September 9, 2015
Progressive increase of T1 signal intensity in the dentate nucleus and globus pallidus on unenhanced T1-weighted MR images in the pediatric brain exposed to multiple doses of gadolinium contrastDonna R Roberts, Kenton R HoldenBrain & Development|January 5, 2016
A splicing mutation of proteolipid protein 1 in Pelizaeus-Merzbacher diseaseTaku Omata, Jun-Ichi Nagai, Hiroko Shimbo, et al.Brain & Development|January 8, 2016
Autoimmune autonomic ganglionopathy in a pediatric patient presenting with acute encephalitisIchiro Kuki, Hisashi Kawawaki, Shin Okazaki, et al.Brain & Development|January 13, 2016
Exome sequencing analysis in a pair of monozygotic twins re-evaluates the genetics behind their intellectual disability and reveals a CHD2 mutationAnna Maria Pinto, Laura Bianciardi, Maria Antonietta Mencarelli, et al.Pageof 478