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Agalsidase alfa and agalsidase beta in the treatment of fabry disease: Does the dose really matter?

Academic Article
Publication Date:
2015
abstract:
Agalsidase alfa was well tolerated throughout the observation period, and no clinical problem occurred after the reintroduction of agalsidase beta in patients who switched back. Despite the exiguous number of patients involved in this observation, and considering that 80% of the patients treated with this drug were males, who are more prone to disease progression, these data offer further information about the safety and efficacy of agalsidase alfa.
Iris type:
01.01 Articolo in rivista
Keywords:
fabry disease
List of contributors:
Riccio, Eleonora
Handle:
https://iris.cnr.it/handle/20.500.14243/405061
Published in:
GENETICS IN MEDICINE
Journal
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http://www.scopus.com/record/display.url?eid=2-s2.0-84920517443&origin=inward
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