A survey on the patient journey in Fabry disease in Japan
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference19 articles.
1. Time delays in the diagnosis and treatment of Fabry disease;Reisin;Int. J. Clin. Pract.,2017
2. Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry outcome survey;Mehta;Eur. J. Clin. Invest.,2004
3. Newborn screening for Fabry disease in the western region of Japan;Sawada;Mol. Genet. Metab. Rep.,2020
4. Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset GLA mutation c.936+919G>a (IVS4+919G>a);Hwu;Hum. Mutat.,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. Right heart and left atrial strain to differentiate cardiac amyloidosis and Fabry disease;Scientific Reports;2024-01-30
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