Angiokeratoma regression in a Fabry disease after treatment with agalsidase-β: clinical effectiveness marker?
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2009.03455.x/fullpdf
Reference5 articles.
1. Fabry disease: an atypical presentation;Choudhury;Pediatr Dermatol,2005
2. The relationship of vascular glycolipid storage to clinical manifestations of Fabry disease: a cross-sectional study of a large cohort of afflicted heterozygote women;Gupta;Medicine,2005
3. Fabry disease: more than angiokeratomas;Mohrenschlager;Arch Dermatol,2004
4. Long-term safety and efficacy of enzyme replacement therapy for Fabry disease;Wilcox;Am J Hum Genet,2004
5. Fabry disease: angiokeratoma, biomarker, and the effect of enzyme replacement therapy on kidney function;Ries;Arch Dermatol,2005
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1. Dermatological Manifestations in Fabry Disease;Amyloidosis and Fabry Disease;2023
2. Angiokeratomas and treatment with enzyme replacement therapy in a patient with Fabry disease;Acta Dermatovenerologica Alpina Pannonica et Adriatica;2020
3. The effect of enzyme replacement therapy on clinical outcomes in male patients with Fabry disease: A systematic literature review by a European panel of experts;Molecular Genetics and Metabolism Reports;2019-06
4. Thrombotic phenomena in angiokeratoma can evolve into spontaneous involution of the lesions: a report of two cases;Journal of Cutaneous Pathology;2015-09-22
5. Angiokeratoma in Fabry Disease: Diagnostic but not Treatment Effectiveness Marker;Global Journal of Medical and Clinical Case Reports;2014-10-15
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