An observational study to investigate the relationship between plasma glucosylsphingosine (lyso-Gb1) concentration and treatment outcomes of patients with Gaucher disease in Japan
Ida, Hiroyuki, Watanabe, Yuko, Sagara, Rieko, Inoue, Yoichi, Fernandez, Jovelle
Published in Orphanet journal of rare diseases (03.11.2022)
Published in Orphanet journal of rare diseases (03.11.2022)
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Journal Article
Re-Evaluations of Zr-DFO Complex Coordination Chemistry for the Estimation of Radiochemical Yields and Chelator-to-Antibody Ratios of 89Zr Immune-PET Tracers
Imura, Ryota, Ida, Hiroyuki, Sasaki, Ichiro, Ishioka, Noriko S., Watanabe, Shigeki
Published in Molecules (Basel, Switzerland) (17.08.2021)
Published in Molecules (Basel, Switzerland) (17.08.2021)
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Long-term safety and effectiveness of velaglucerase alfa in Gaucher disease: 6-year interim analysis of a post-marketing surveillance in Japan
Sagara, Rieko, Ishigaki, Masahide, Otsuka, Manami, Murayama, Kei, Ida, Hiroyuki, Fernandez, Jovelle
Published in Orphanet journal of rare diseases (04.12.2021)
Published in Orphanet journal of rare diseases (04.12.2021)
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Journal Article
Chaperone effect of sulfated disaccharide from heparin on mutant iduronate-2-sulfatase in mucopolysaccharidosis type II
Hoshina, Hiroo, Shimada, Yohta, Higuchi, Takashi, Kobayashi, Hiroshi, Ida, Hiroyuki, Ohashi, Toya
Published in Molecular genetics and metabolism (01.02.2018)
Published in Molecular genetics and metabolism (01.02.2018)
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Journal Article
Efficient engraftment of genetically modified cells is necessary to ameliorate central nervous system involvement of murine model of mucopolysaccharidosis type II by hematopoietic stem cell targeted gene therapy
Miwa, Saori, Watabe, Ayako M., Shimada, Yohta, Higuchi, Takashi, Kobayashi, Hiroshi, Fukuda, Takahiro, Kato, Fusao, Ida, Hiroyuki, Ohashi, Toya
Published in Molecular genetics and metabolism (01.08.2020)
Published in Molecular genetics and metabolism (01.08.2020)
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Journal Article
Mutation spectrum of α-Galactosidase gene in Japanese patients with Fabry disease
Kobayashi, Masahisa, Ohashi, Toya, Kaneshiro, Eiko, Higuchi, Takashi, Ida, Hiroyuki
Published in Journal of human genetics (01.07.2019)
Published in Journal of human genetics (01.07.2019)
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Journal Article
Pectus carinatum as the key to early diagnosis of Morquio A syndrome: a case report
Yamauchi, Kento, Hirano, Daishi, Wada, Miho, Ida, Hiroyuki
Published in Journal of medical case reports (05.04.2021)
Published in Journal of medical case reports (05.04.2021)
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Journal Article
The function of Scox in glial cells is essential for locomotive ability in Drosophila
Kowada, Ryosuke, Kodani, Atsushi, Ida, Hiroyuki, Yamaguchi, Masamitsu, Lee, Im-Soon, Okada, Yasushi, Yoshida, Hideki
Published in Scientific reports (27.10.2021)
Published in Scientific reports (27.10.2021)
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Journal Article
Hematopoietic Stem Cell Gene Therapy Corrects Neuropathic Phenotype in Murine Model of Mucopolysaccharidosis Type II
Wakabayashi, Taichi, Shimada, Yohta, Akiyama, Kazumasa, Higuchi, Takashi, Fukuda, Takahiro, Kobayashi, Hiroshi, Eto, Yoshikatsu, Ida, Hiroyuki, Ohashi, Toya
Published in Human gene therapy (01.06.2015)
Published in Human gene therapy (01.06.2015)
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Journal Article
Pulmonary hypertension due to left heart disease causes intrapulmonary venous arterialization in rats
Fujimoto, Yoshitaka, Urashima, Takashi, Kawachi, Fumie, Akaike, Toru, Kusakari, Yoichiro, Ida, Hiroyuki, Minamisawa, Susumu
Published in The Journal of thoracic and cardiovascular surgery (01.11.2017)
Published in The Journal of thoracic and cardiovascular surgery (01.11.2017)
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Journal Article
Clinical assessment of upper airway and its complications in Hunter syndrome
Iijima, Masatoshi, Hirano, Daishi, Yokoi, Kentaro, Kobayashi, Hiroshi, Fujiwara, Masako, Ida, Hiroyuki, Oishi, Kimihiko
Published in Pediatrics international (01.05.2021)
Published in Pediatrics international (01.05.2021)
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