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Randomized trial of vitamin D supplementation to prevent seasonal influenza A in schoolchildren

The American journal of clinical nutrition, 2010-05, Vol.91 (5), p.1255-1260

2010

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Obituary: Toshiyuki Fukao (1961-2020), a friend of the Latin American IEM community

Journal of inborn errors of metabolism and screening, 2020-07, Vol.8

Ida, Hiroyuki

2020

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Gaucher disease types 1 and 3: Phenotypic characterization of large populations from the ICGG Gaucher Registry

American journal of hematology, 2015-07, Vol.90 (S1), p.S12-S18

2015

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An observational study to investigate the relationship between plasma glucosylsphingosine (lyso-Gb1) concentration and treatment outcomes of patients with Gaucher disease in Japan

Orphanet journal of rare diseases, 2022-11, Vol.17 (1), p.1-401, Article 401

2022

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Re-Evaluations of Zr-DFO Complex Coordination Chemistry for the Estimation of Radiochemical Yields and Chelator-to-Antibody Ratios of 89Zr Immune-PET Tracers

Molecules (Basel, Switzerland), 2021-08, Vol.26 (16), p.4977

2021

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Allele frequency of pathogenic variants causing acid sphingomyelinase deficiency and Gaucher disease in the general Japanese population

Human genome variation, 2024-06, Vol.11 (1), p.24-5, Article 24

2024

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Treatment Satisfaction and Its Influencing Factors in Parkinson’s Disease: A Web-Based Survey of Patients and Physicians in Clinical Practice in Japan

Parkinson's disease, 2022-02, Vol.2022, p.2732021-13

2022

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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

Orphanet journal of rare diseases, 2021-12, Vol.16 (1), p.502-502, Article 502

2021

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Chaperone effect of sulfated disaccharide from heparin on mutant iduronate-2-sulfatase in mucopolysaccharidosis type II

Molecular genetics and metabolism, 2018-02, Vol.123 (2), p.118-122

2018

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Anti-BlyS antibody reduces the immune reaction against enzyme and enhances the efficacy of enzyme replacement therapy in Fabry disease model mice

Clinical immunology (Orlando, Fla.), 2017-05, Vol.178, p.56-63

2017

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Mutation spectrum of α-Galactosidase gene in Japanese patients with Fabry disease

Journal of human genetics, 2019-07, Vol.64 (7), p.695-699

2019

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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

Molecular genetics and metabolism, 2020-08, Vol.130 (4), p.262-273

2020

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Pectus carinatum as the key to early diagnosis of Morquio A syndrome: a case report

Journal of medical case reports, 2021-04, Vol.15 (1), p.150-150, Article 150

2021

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Increased food allergy and vitamin D: Randomized, double-blind, placebo-controlled trial

Pediatrics international, 2014-02, Vol.56 (1), p.6-12

2014

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The function of Scox in glial cells is essential for locomotive ability in Drosophila

Scientific reports, 2021-10, Vol.11 (1), p.21207-21207, Article 21207

2021

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Pulmonary hypertension due to left heart disease causes intrapulmonary venous arterialization in rats

The Journal of thoracic and cardiovascular surgery, 2017-11, Vol.154 (5), p.1742-1753.e8

2017

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Hematopoietic Stem Cell Gene Therapy Corrects Neuropathic Phenotype in Murine Model of Mucopolysaccharidosis Type II

Human gene therapy, 2015-06, Vol.26 (6), p.357

2015

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Clinical assessment of upper airway and its complications in Hunter syndrome

Pediatrics international, 2021-05, Vol.63 (5), p.543-549

2021

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Clinical findings of gadolinium-enhanced cardiac magnetic resonance in Fabry patients

Journal of cardiology, 2020-01, Vol.75 (1), p.27-33

2020

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Accurate and Precise Viscosity Measurements of Gelatin Solutions Using a Rotational Rheometer

Food Science and Technology Research, 2019, Vol.25(2), pp.217-226

2019

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A Japanese Patient with Gaucher Disease Treated with the Oral Drug Eliglustat as Substrate Reducing Therapy

Case reports in gastroenterology, 2021-09, Vol.15 (3), p.838-845

2021

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Binding affinity of ssDNA is improved by attachment of dsDNA regions

Journal of bioscience and bioengineering, 2014-09, Vol.118 (3), p.239-241

2014

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Oral alendronate in pediatric chronic recurrent multifocal osteomyelitis

Pediatrics international, 2017-04, Vol.59 (4), p.506-508

2017

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Characteristics of Japanese patients with X-linked adrenoleukodystrophy and concerns of their families from the 1st registry system

Brain & development (Tokyo. 1979), 2019-01, Vol.41 (1), p.50-56

2019

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Hematopoietic stem cell gene therapy ameliorates CNS involvement in murine model of GM1-gangliosidosis

Molecular therapy. Methods & clinical development, 2022-06, Vol.25, p.448-460

2022

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Randomized trial of vitamin D supplementation to prevent seasonal influenza A in schoolchildren

Obituary: Toshiyuki Fukao (1961-2020), a friend of the Latin American IEM community

Gaucher disease types 1 and 3: Phenotypic characterization of large populations from the ICGG Gaucher Registry

An observational study to investigate the relationship between plasma glucosylsphingosine (lyso-Gb1) concentration and treatment outcomes of patients with Gaucher disease in Japan

Re-Evaluations of Zr-DFO Complex Coordination Chemistry for the Estimation of Radiochemical Yields and Chelator-to-Antibody Ratios of 89Zr Immune-PET Tracers

Allele frequency of pathogenic variants causing acid sphingomyelinase deficiency and Gaucher disease in the general Japanese population

Treatment Satisfaction and Its Influencing Factors in Parkinson’s Disease: A Web-Based Survey of Patients and Physicians in Clinical Practice in Japan

Long-term safety and effectiveness of velaglucerase alfa in Gaucher disease: 6-year interim analysis of a post-marketing surveillance in Japan

Chaperone effect of sulfated disaccharide from heparin on mutant iduronate-2-sulfatase in mucopolysaccharidosis type II

Anti-BlyS antibody reduces the immune reaction against enzyme and enhances the efficacy of enzyme replacement therapy in Fabry disease model mice

Mutation spectrum of α-Galactosidase gene in Japanese patients with Fabry disease

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

Pectus carinatum as the key to early diagnosis of Morquio A syndrome: a case report

Increased food allergy and vitamin D: Randomized, double-blind, placebo-controlled trial

The function of Scox in glial cells is essential for locomotive ability in Drosophila

Pulmonary hypertension due to left heart disease causes intrapulmonary venous arterialization in rats

Hematopoietic Stem Cell Gene Therapy Corrects Neuropathic Phenotype in Murine Model of Mucopolysaccharidosis Type II

Clinical assessment of upper airway and its complications in Hunter syndrome

Clinical findings of gadolinium-enhanced cardiac magnetic resonance in Fabry patients

Accurate and Precise Viscosity Measurements of Gelatin Solutions Using a Rotational Rheometer

A Japanese Patient with Gaucher Disease Treated with the Oral Drug Eliglustat as Substrate Reducing Therapy

Binding affinity of ssDNA is improved by attachment of dsDNA regions

Oral alendronate in pediatric chronic recurrent multifocal osteomyelitis

Characteristics of Japanese patients with X-linked adrenoleukodystrophy and concerns of their families from the 1st registry system

Hematopoietic stem cell gene therapy ameliorates CNS involvement in murine model of GM1-gangliosidosis

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