Showing results (761-770 of 905) with videos related to
Sort By:
Pageof 91
Neurosurgery|June 13, 2013
Postoperative increase in cerebral white matter fractional anisotropy on diffusion tensor magnetic resonance imaging is associated with cognitive improvement after uncomplicated carotid endarterectomy: tract-based spatial statistics analysisYuiko Sato, Kenji Ito, Kuniaki Ogasawara, et al.Autoimmunity|November 27, 2018
Polymorphisms in Th17-related genes and the pathogenesis of autoimmune thyroid diseaseTakayuki Kunisato, Mikio Watanabe, Naoya Inoue, et al.Autoimmunity|March 12, 2015
Reactivation of persistent Epstein-Barr virus (EBV) causes secretion of thyrotropin receptor antibodies (TRAbs) in EBV-infected B lymphocytes with TRAbs on their surfaceKeiko Nagata, Yuji Nakayama, Katsumi Higaki, et al.Acta Medica Okayama|June 24, 2015
Aberrant Expression of Keratin 7 in Hepatocytes as a Predictive Marker of Rapid Progression to Hepatic Failure in Asymptomatic Primary Biliary CirrhosisHiroyuki Seki, Fusao Ikeda, Shintaro Nanba, et al.Hinyokika Kiyo. Acta Urologica Japonica|March 30, 2026
[A Case of Asymptomatic Paraganglioma of the Bladder]Taito Sato, Naoki Hayata, Takuya Hida, et al.ACS Applied Materials & Interfaces|May 16, 2013
Nano-micrometer-architectural acidic silica prepared from iron oxide of Leptothrix ochracea originHideki Hashimoto, Atsushi Itadani, Takayuki Kudoh, et al.Hypertension (Dallas, Tex. : 1979)|December 3, 2019
Comprehensive Analysis of Steroid Biomarkers for Guiding Primary Aldosteronism SubtypingAdina F Turcu, Taweesak Wannachalee, Alexander Tsodikov, et al.European Journal of Clinical Investigation|June 26, 2001
Mitochondrial DNA deletion associated with the reduction of adenine nucleotides in human atrium and atrial fibrillationM Tsuboi, I Hisatome, T Morisaki, et al.Plos One|October 16, 2009
Generation and characterization of conditional heparin-binding EGF-like growth factor knockout miceAtsushi Oyagi, Yasuhisa Oida, Kenichi Kakefuda, et al.Internal Medicine (Tokyo, Japan)|December 22, 2011
Novel mutations in the gene encoding acid α-1,4-glucosidase in a patient with late-onset glycogen storage disease type II (Pompe disease) with impaired intelligenceTomie Muraoka, Koji Murao, Hitomi Imachi, et al.Pageof 91