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Journal of Inherited Metabolic Disease
|
October 9, 2024
A phase III, open-label clinical trial evaluating pegunigalsidase alfa administered every 4 weeks in adults with Fabry disease previously treated with other enzyme replacement therapies
Myrl Holida, Aleš Linhart, Antonio Pisani, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 11, 2018
Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?
Juan Politei, Valeria Alberton, Oscar Amoreo, et al.
Nature Communications
|
January 10, 2026
Lucerastat, an oral therapy for Fabry disease: results from a pivotal randomized phase 3 study and its open-label extension
Peter Nordbeck, Ozlem Goker-Alpan, John A Bernat, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 63) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 63 results.
Journal of Inherited Metabolic Disease
|
October 9, 2024
A phase III, open-label clinical trial evaluating pegunigalsidase alfa administered every 4 weeks in adults with Fabry disease previously treated with other enzyme replacement therapies
Myrl Holida, Aleš Linhart, Antonio Pisani, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 11, 2018
Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?
Juan Politei, Valeria Alberton, Oscar Amoreo, et al.
Nature Communications
|
January 10, 2026
Lucerastat, an oral therapy for Fabry disease: results from a pivotal randomized phase 3 study and its open-label extension
Peter Nordbeck, Ozlem Goker-Alpan, John A Bernat, et al.
Page
of 7