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International Journal of Molecular Sciences|January 16, 2020
Novel Enzyme Replacement Therapies for Neuropathic MucopolysaccharidosesYuji Sato, Torayuki OkuyamaMolecular Genetics and Metabolism Reports|July 21, 2017
Enzyme activities of α-glucosidase in Japanese neonates with pseudodeficiency allelesRyuichi Mashima, Torayuki OkuyamaRedox Biology|August 24, 2015
The role of lipoxygenases in pathophysiology; new insights and future perspectivesRyuichi Mashima, Torayuki OkuyamaMolecular Genetics and Metabolism Reports|October 7, 2017
Enzyme replacement therapy attenuates disease progression in two Japanese siblings with mucopolysaccharidosis type VI: 10-Year follow upMahoko Furujo, Motomichi Kosuga, Torayuki OkuyamaNihon Rinsho. Japanese Journal of Clinical Medicine|March 19, 2005
[Genetic medicine in Japan]Torayuki Okuyama, Rika Kosaki, Yasuyuki FukuharaInternational Journal of Molecular Sciences|April 17, 2020
Biomarkers for Lysosomal Storage Disorders with an Emphasis on Mass SpectrometryRyuichi Mashima, Torayuki Okuyama, Mari OhiraFuture Science OA|January 10, 2020
Biosynthesis of long chain base in sphingolipids in animals, plants and fungiRyuichi Mashima, Torayuki Okuyama, Mari OhiraMolecular Genetics and Metabolism Reports|October 13, 2025
Case report of neuronopathic mucopolysaccharidosis type II: Early intracerebroventricular enzyme replacement therapy and hematopoietic cell transplantation with developmental outcomes up to 5 years of ageAzuma Ikari, Asahito Hama, Torayuki OkuyamaInternational Journal of Molecular Sciences|February 26, 2022
Physiology and Pathophysiology of Heparan Sulfate in Animal Models: Its Biosynthesis and DegradationRyuichi Mashima, Torayuki Okuyama, Mari OhiraPageof 12