Shared decision making between patients with Fabry disease and physicians in Japan: An online survey-Reference-Cited by-同舟云学术

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Shared decision making between patients with Fabry disease and physicians in Japan: An online survey

Published:2022-09 Issue: Volume:32 Page:100899
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Inagaki Natsuko,Tsuchiya Mio,Otani Kazuki,Nakayama Takeo

Funder

Amicus Therapeutics

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference26 articles.

1. Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency;Brady;N. Engl. J. Med.,1967

2. Fabry Disease. [Updated 2021 Jul 10];Bokhari,2021

3. Fabry disease;Germain;Orphanet. J. Rare Dis.,2010

4. Fabry's disease: alpha-galactosidase deficiency;Kint;Science.,1970

5. Psychological aspects of patients with Fabry disease;Crosbie;J. Inherit. Metab. Dis.,2009

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Patient-reported experience with Fabry disease and its management in the real-world setting: results from a double-blind, cross-sectional survey of 280 respondents;Orphanet Journal of Rare Diseases;2024-04-11

2. Editorial: Shared decision-making in neurology;Frontiers in Neurology;2023-06-06

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