Cardiac Manifestations in Fabry Disease
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-17759-0_26
Reference48 articles.
1. Garman SC, Garboczi DN. The molecular defect leading to fabry disease: structure of human α-galactosidase. J Mol Biol. 2004;337:319–35. https://doi.org/10.1016/j.jmb.2004.01.035.
2. Ortiz A, Abiose A, Bichet DG, Cabrera G, Charrow J, Germain DP, et al. Time to treatment benefit for adult patients with Fabry disease receiving agalsidase β: data from the Fabry registry. J Med Genet. 2016;53:495–502. https://doi.org/10.1136/jmedgenet-2015-103486.
3. Pieroni M, Moon JC, Arbustini E, Barriales-Villa R, Camporeale A, Vujkovac AC, et al. Cardiac involvement in Fabry disease: JACC review topic of the week. J Am Coll Cardiol. 2021;77:922–36. https://doi.org/10.1016/j.jacc.2020.12.024.
4. Frustaci A, Chimenti C, Ricci R, Natale L, Russo MA, Pieroni M, et al. Improvement in cardiac function in the cardiac variant of Fabry’s disease with galactose-infusion therapy. N Engl J Med. 2001;345:25–32. https://doi.org/10.1056/NEJM200107053450104.
5. Banikazemi M. Agalsidase-Beta therapy for advanced Fabry disease. Ann Intern Med. 2007;146:77. https://doi.org/10.7326/0003-4819-146-2-200701160-00148.
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