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American Journal of Ophthalmology Case Reports|March 7, 2020
Macular hole and serous pigment epithelial detachment in bilateral acquired vitelliform lesionsNana Yata, Tsutomu Yasukawa, Mihoko Kawamura, et al.The Journal of Biological Chemistry|July 24, 2009
Brain-derived neurotrophic factor enhances the basal rate of protein synthesis by increasing active eukaryotic elongation factor 2 levels and promoting translation elongation in cortical neuronsNobuyuki Takei, Mihoko Kawamura, Yuta Ishizuka, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 5, 2004
Brain-derived neurotrophic factor induces mammalian target of rapamycin-dependent local activation of translation machinery and protein synthesis in neuronal dendritesNobuyuki Takei, Naoko Inamura, Mihoko Kawamura, et al.Clinical Ophthalmology (Auckland, N.Z.)|August 30, 2018
Six-month results of intravitreal ranibizumab for macular edema after branch retinal vein occlusion in a single-center prospective study: visual outcomes and microaneurysm formationMihoko Kawamura, Yoshio Hirano, Munenori Yoshida, et al.Seminars in Ophthalmology|February 22, 2021
Twenty-Four Month Results of Intravitreal Ranibizumab for Macular Edema after Branch Retinal Vein Occlusion: Visual Outcomes and Resolution of Macular EdemaMiho Inagaki, Yoshio Hirano, Yusuke Yasuda, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|January 8, 2014
Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compactionSeiko Ohno, Masato Omura, Mihoko Kawamura, et al.Circulation Journal : Official Journal of the Japanese Circulation Society|December 17, 2008
Dynamic change in ST-segment and spontaneous occurrence of ventricular fibrillation in Brugada syndrome with a novel nonsense mutation in the SCN5A gene during long-term follow-upMihoko Kawamura, Tomoya Ozawa, Takenori Yao, et al.Circulation Journal : Official Journal of the Japanese Circulation Society|October 27, 2010
Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndromeYuko Oka, Hideki Itoh, Wei-Guang Ding, et al.Circulation Journal : Official Journal of the Japanese Circulation Society|July 13, 2012
Seasonal and circadian distributions of cardiac events in genotyped patients with congenital long QT syndromeMasateru Takigawa, Mihoko Kawamura, Takashi Noda, et al.Journal of the American College of Cardiology|August 22, 2009
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndromeYukiko Nishio, Takeru Makiyama, Hideki Itoh, et al.Pageof 2