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Rinsho Shinkeigaku = Clinical Neurology|May 31, 2019
[Current status and future prospect of enzyme replacement therapy for Fabry disease]Toya OhashiJournal of Human Genetics|December 1, 2018
Gene therapy for lysosomal storage diseases and peroxisomal diseasesToya OhashiNihon Rinsho. Japanese Journal of Clinical Medicine|March 19, 2005
[Gene analysis of Gaucher disease]Toya OhashiPediatric Endocrinology Reviews : PER|January 22, 2013
Enzyme replacement therapy for lysosomal storage diseasesToya OhashiCurrent Molecular Medicine|March 20, 2002
Novel treatment for neuronopathic lysosomal storage diseases--cell therapy/gene therapyYoshikatsu Eto, Toya OhashiClinical Immunology (Orlando, Fla.)|February 6, 2017
Anti-BlyS antibody reduces the immune reaction against enzyme and enhances the efficacy of enzyme replacement therapy in Fabry disease model miceYohei Sato, Hiroyuki Ida, Toya OhashiMolecular Genetics and Metabolism|May 6, 2008
Reduced alpha-Gal A enzyme activity in Fabry fibroblast cells and Fabry mice tissues induced by serum from antibody positive patients with Fabry diseaseToya Ohashi, Sayoko Iizuka, Hiroyuki Ida, et al.Molecular Genetics and Metabolism|May 31, 2024
Usefulness of antibody-drug conjugate as preconditioning for hematopoietic stem cell-targeted gene therapy in wild-type and Fabry disease mouse modelsJin Ogata, Yohta Shimada, Toya Ohashi, et al.Molecular Genetics and Metabolism|August 3, 2013
Enzyme replacement therapy in two Japanese siblings with Fabry disease, and its effectiveness on angiokeratoma and neuropathic painMahoko Furujo, Toshihide Kubo, Masahisa Kobayashi, et al.Cureus|September 26, 2024
Cochlear Implantation for Isoleucyl-tRNA Synthetase Mutation-Associated Mitochondrial Disease: A Case ReportMasaomi Motegi, Yuika Sakurai, Yasushi Mio, et al.Pageof 14