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No to Hattatsu = Brain and Development|August 27, 2014
[Successful treatment with intravenous steroid pulse therapy of a boy with recurrent idiopathic sixth nerve palsy]Keitaro Yamada, Tomokazu Kimizu, Sadami Kimura, et al.Journal of Child Neurology|October 5, 2011
Prolonged elevation of serum neuron-specific enolase in children after clinical diagnosis of brain deathYasuhiro Suzuki, Yukiko Mogami, Yausihisa Toribe, et al.Molecular Genetics and Metabolism|June 13, 2006
A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiencyToshiyuki Fukao, Satomi Sakurai, Marie-Odile Rolland, et al.Journal of Human Genetics|July 2, 2021
Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature reviewKazuki Watanabe, Mitsuko Nakashima, Satoko Kumada, et al.Molecular Genetics & Genomic Medicine|May 21, 2019
Identification of novel compound heterozygous mutations in ACO2 in a patient with progressive cerebral and cerebellar atrophyMasahide Fukada, Keitaro Yamada, Shima Eda, et al.No to Hattatsu = Brain and Development|March 16, 2011
[Changes of brain edema after initiation of mild hypothermia therapy in children]Keitaro Yamada, Toshiyuki Mano, Yu Inada, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|September 22, 2010
Clinical aspects of very-low-birthweight infants showing reopening of ductus arteriosusAtsushi Uchiyama, Hiroyuki Nagasawa, Yutaka Yamamoto, et al.Molecular Genetics and Metabolism|December 16, 2006
Single-base substitution at the last nucleotide of exon 6 (c.671G>A), resulting in the skipping of exon 6, and exons 6 and 7 in human succinyl-CoA:3-ketoacid CoA transferase (SCOT) geneKeitaro Yamada, Toshiyuki Fukao, Gaixiu Zhang, et al.Seizure|June 19, 2014
Predictive value of EEG findings at control of epileptic spasms for seizure relapse in patients with West syndromeKeitaro Yamada, Yasuhisa Toribe, Tomokazu Kimizu, et al.Brain & Development|June 4, 2016
Arts syndrome with a novel missense mutation in the PRPS1 gene: A case reportKoichi Maruyama, Shunsuke Ogaya, Naoko Kurahashi, et al.Pageof 4