Fabry's Disease (Angiokeratoma Corporis Diffusum)
Author:
Publisher
American College of Physicians
Subject
General Medicine,Internal Medicine
Cited by 31 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. Global reach of over 20 years of experience in the patient-centered Fabry Registry: Advancement of Fabry disease expertise and dissemination of real-world evidence to the Fabry community;Molecular Genetics and Metabolism;2023-07
2. Urinary mulberry bodies as a potential biomarker for early diagnosis and efficacy assessment of enzyme replacement therapy in Fabry nephropathy;Nephrology Dialysis Transplantation;2020-12-24
3. Abnormal expression and processing of uromodulin in Fabry disease reflects tubular cell storage alteration and is reversible by enzyme replacement therapy;Journal of Inherited Metabolic Disease;2008-07-27
4. Postmortem diagnosis of Fabry disease with acromegaly and a unique vasculopathy;Virchows Archiv;2007-07-12
5. Fabry disease in a heterozygote presenting as hand ischaemia and painful acroparaesthesia;Australasian Journal of Dermatology;2007-02
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