Long-term efficacy and safety of pegunigalsidase alfa administered every 4 weeks in adults with Fabry disease: results from up to 5 years of the BRIGHT F51 phase III, open-label extension study. [PDF]
Holida M +19 more
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A rapid method to reduce drug interferences for antibody measurements in pegunigalsidase alfa-treated patients with Fabry disease. [PDF]
Lenders M +4 more
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Impaired motor unit profile in Fabry disease: A quantitative electrophysiological study. [PDF]
Gunduz A +4 more
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Prevalence and sociodemographic, clinical, and genetic characteristics of Fabry disease in north-central Chile, 2013-2023. [PDF]
Royo Martínez S +4 more
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Bridging Biochemical and Clinical Disease Burden in Fabry Disease: A Comparative Analysis of Lyso-Gb3, MSSI, DS3, and FASTEX. [PDF]
Ozturk S, Akyol EMB.
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Cardiological aspects of Fabry disease: from diagnosis to therapeutic efficacy assessment. [PDF]
Graziani F +9 more
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Integrated Glyco-Analytical Strategy for Comprehensive Characterization of a Complex Therapeutic Glycoprotein: Fabrazyme. [PDF]
Afonin M +3 more
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Impact of Proteinuria on Renal Outcomes in the BALANCE Trial. [PDF]
Wallace EL +7 more
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Therapeutic landscape of Fabry disease: advances and challenges from classical strategies to emerging therapies. [PDF]
Zhang M, Wang C.
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