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Published in 2022 at "Orphanet Journal of Rare Diseases"
DOI: 10.1186/s13023-022-02175-2
Abstract: Background Enzyme replacement therapy (ERT) with recombinant human alpha-glucosidase (rhGAA, alglucosidase alfa) has improved survival, motor outcomes, daily life activity and quality of life in Pompe patients. However, ERT in Pompe disease often induces formation…
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Keywords:
alpha glucosidase;
antibody titers;
antibody;
human alpha ... See more keywords