Kenichi Hongo, Toru Harada, Eiko Fukuro, Masahisa Kobayashi, Toya Ohashi, Yoshikatsu Eto. Massive accumulation of globotriaosylceramide in various tissues from a Fabry patient with a high antibody titer against alpha-galactosidase A after 6 years of enzyme replacement therapy. Molecular genetics and metabolism reports. 2020. 24. 100623-100623
Satoshi Morimoto, Ayumi Nojiri, Eiko Fukuro, Ikuko Anan, Makoto Kawai, Ken Sakurai, Masahisa Kobayashi, Hiroshi Kobayashi, Hiroyuki Ida, Toya Ohashi, et al. Characteristics of the Electrocardiogram in Japanese Fabry Patients Under Long-Term Enzyme Replacement Therapy. Frontiers in cardiovascular medicine. 2020. 7. 614129-614129
Masahisa Kobayashi, Toya Ohashi, Eiko Kaneshiro, Takashi Higuchi, Hiroyuki Ida. Mutation spectrum of α-Galactosidase gene in Japanese patients with Fabry disease. Journal of Human Genetics. 2019. 64. 7. 695-699
Kenichi Hongo, Keiichi Ito, Taro Date, Ikuko Anan, Yasunori Inoue, Satoshi Morimoto, Kazuo Ogawa, Makoto Kawai, Hiroshi Kobayashi, Masahisa Kobayashi, et al. The beneficial effects of long-term enzyme replacement therapy on cardiac involvement in Japanese Fabry patients. MOLECULAR GENETICS AND METABOLISM. 2018. 124. 2. 143-151
Ken Takagi, Masahisa Kobayashi, Masako Fujiwara, Toya Ohashi, Kiyoshi Ogawa, Yoshikatsu Eto, Hiroyuki Ida. Cardiac Characteristics of Fabry Disease in Japanese Children and Adolescents (Original). Jikeikai medical journal. 2014. 61. 4. 65-75
M. Kobayashi, T. Ohashi, T. Fukuda, Y. Eto, H. Ida. The clinical, genetic and pathological studies of 5 Japanese patients with perinatal lethal Gaucher disease. JOURNAL OF INHERITED METABOLIC DISEASE. 2008. 31. 95-95