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Physical Chemistry Chemical Physics : PCCP|June 22, 2022
Operando resonant soft X-ray emission spectroscopy of the LiMn2O4 cathode using an aqueous electrolyte solutionDaisuke Asakura, Yusuke Nanba, Hideharu Niwa, et al.Neuroradiology|August 5, 2017
Apparent brain temperature imaging with multi-voxel proton magnetic resonance spectroscopy compared with cerebral blood flow and metabolism imaging on positron emission tomography in patients with unilateral chronic major cerebral artery steno-occlusive diseaseTakamasa Nanba, Hideaki Nishimoto, Yoshichika Yoshioka, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|July 20, 2017
Pharmacoresistant epileptic eyelid twitching in a child with a mutation in SYNGAP1Tetsuya Okazaki, Yoshiaki Saito, Rika Hiraiwa, et al.DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|May 15, 2004
Coordinate downregulation of a novel imprinted transcript ITUP1 with PEG3 in glioma cell linesShinji Maegawa, Noriko Itaba, Susumu Otsuka, et al.Bioscience, Biotechnology, and Biochemistry|December 4, 1998
Immobilization of N-carbamyl-D-amino acid amidohydrolaseH Nanba, Y Ikenaka, Y Yamada, et al.Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|December 17, 2009
Procalcitonin and severity of community-acquired pneumoniaNiro Okimoto, Yoshikiyo Hayashi, Mitsunori Ishiga, et al.Angewandte Chemie (International Ed. in English)|February 14, 2018
Solid-Solution Alloy Nanoparticles of the Immiscible Iridium-Copper System with a Wide Composition Range for Enhanced Electrocatalytic ApplicationsFenglong Wang, Kohei Kusada, Dongshuang Wu, et al.Human Genome Variation|February 2, 2017
A novel SLC34A2 mutation in a patient with pulmonary alveolar microlithiasisHiroki Izumi, Jun Kurai, Masahiro Kodani, et al.Yonago Acta Medica|August 6, 2016
Clinical Diagnosis of Mendelian Disorders Using a Comprehensive Gene-Targeted Panel Test for Next-Generation SequencingTetsuya Okazaki, Megumi Murata, Masachika Kai, et al.Human Genome Variation|May 1, 2020
Duchenne muscular dystrophy-like phenotype in an LGMD2I patient with novel FKRP gene variantsTetsuya Okazaki, Kaori Matsuura, Noriko Kasagi, et al.Pageof 91