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Journal of Neurology, Neurosurgery, and Psychiatry|April 19, 2018
Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trialYutaka Ohsawa, Hiroki Hagiwara, Shin-Ichiro Nishimatsu, et al.Biological & Pharmaceutical Bulletin|July 3, 2020
Investigating DNA Methylation of SHATI/NAT8L Promoter Sites in Blood of Unmedicated Patients with Major Depressive DisorderHajime Miyanishi, Kyosuke Uno, Mina Iwata, et al.American Journal of Medical Genetics. Part A|April 25, 2012
The incidence of hypoplasia of the corpus callosum in patients with dup (X)(q28) involving MECP2 is associated with the location of distal breakpointsShozo Honda, Shin Hayashi, Takaya Nakane, et al.Cerebral Cortex (New York, N.Y. : 1991)|July 14, 2010
Neocortical layer formation of human developing brains and lissencephalies: consideration of layer-specific marker expressionTakashi Saito, Sae Hanai, Sachio Takashima, et al.The Journal of Pediatrics|December 17, 2018
A Pilot Study of Soluble Form of LOX-1 as a Novel Biomarker for Neonatal Hypoxic-Ischemic EncephalopathyTomohisa Akamatsu, Takehiro Sugiyama, Yoshinori Aoki, et al.Nature Communications|May 16, 2018
CO<sub>2</sub>-sensitive tRNA modification associated with human mitochondrial diseaseHuan Lin, Kenjyo Miyauchi, Tai Harada, et al.BMC Neuroscience|August 10, 2011
The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndromeKunio Miyake, Takae Hirasawa, Masaki Soutome, et al.Molecular Genetics and Metabolism|December 31, 2013
GJC2 promoter mutations causing Pelizaeus-Merzbacher-like diseaseLeo Gotoh, Ken Inoue, Guy Helman, et al.Cold Spring Harbor Molecular Case Studies|August 25, 2019
A novel <i>PAK3</i> pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literatureAritoshi Iida, Kyoko Takano, Eri Takeshita, et al.Journal of Human Genetics|August 8, 2014
A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutationHirotomo Saitsu, Jun Tohyama, Tom Walsh, et al.Pageof 20