H
Hiroyuki Ida
Researcher at Jikei University School of Medicine
Publications - 191
Citations - 3876
Hiroyuki Ida is an academic researcher from Jikei University School of Medicine. The author has contributed to research in topics: Enzyme replacement therapy & Fabry disease. The author has an hindex of 29, co-authored 177 publications receiving 3390 citations.
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Journal ArticleDOI
Randomized trial of vitamin D supplementation to prevent seasonal influenza A in schoolchildren
TL;DR: It is suggested that vitamin D(3) supplementation during the winter may reduce the incidence of influenza A, especially in specific subgroups of schoolchildren.
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Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patients
Neal J. Weinreb,Mario C. Aggio,Hans C. Andersson,Generoso Andria,Joel Charrow,Joe T.R. Clarke,Anders Erikson,P Giraldo,Jack Goldblatt,Carla E. M. Hollak,Hiroyuki Ida,Paige Kaplan,Edwin H. Kolodny,Pramod K. Mistry,Gregory M. Pastores,R. F. Pires,Ainu Prakesh-Cheng,Barry E. Rosenbloom,C. Ronald Scott,Elisa A. P. Sobreira,Anna Tylki-Szymańska,Ashok Vellodi,Stephan vom Dahl,Rebecca S. Wappner,Ari Zimran +24 more
TL;DR: All patients with type 1 Gaucher disease should undergo comprehensive regular assessment, the frequency of which depends on treatment status and whether therapeutic goals have been achieved, and reassessment should be performed whenever enzyme therapy dose is altered, or in case of significant clinical complication.
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Japan Elaprase Treatment (JET) study: idursulfase enzyme replacement therapy in adult patients with attenuated Hunter syndrome (Mucopolysaccharidosis II, MPS II).
Torayuki Okuyama,Akemi Tanaka,Yasuyuki Suzuki,Hiroyuki Ida,Toju Tanaka,Gerald F. Cox,Gerald F. Cox,Yoshikatsu Eto,Tadao Orii +8 more
TL;DR: Idursulfase treatment appears to be safe and effective in adult Japanese patients with attenuated MPS II and advanced disease, comparable to those of prior studies that enrolled predominantly pediatric, Caucasian, and less ill patients.
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N-octyl-beta-valienamine up-regulates activity of F213I mutant beta-glucosidase in cultured cells: a potential chemical chaperone therapy for Gaucher disease.
Hou Lin,Yuko Sugimoto,Yuki Ohsaki,Haruaki Ninomiya,Akira Oka,Miyako Taniguchi,Hiroyuki Ida,Yoshikatsu Eto,Seiichiro Ogawa,Yuji Matsuzaki,Miwa Sawa,Takehiko Inoue,Katsumi Higaki,Eiji Nanba,Kousaku Ohno,Yoshiyuki Suzuki +15 more
TL;DR: It is suggested that NOV works as a chemical chaperone to accelerate transport and maturation of F213I mutant β-Glu and may suggest a therapeutic value of this compound for GD.
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Gaucher disease types 1 and 3: Phenotypic characterization of large populations from the ICGG Gaucher Registry.
TL;DR: The diversity of GBA gene mutations from patients with Gaucher disease represented in the ICGG Gaucher Registry database and in the literature provides the basis for initial genotype/phenotype correlations, the outcomes of which are summarized here.