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Anti-drug antibody formation in Japanese Fabry patients following enzyme replacement therapy

Enzyme replacement therapy (ERT) for Fabry disease (deficiency of α-galactosidase A, α-Gal) with recombinant α-Gals (agalsidase alfa and agalsidase beta) is widely available and improves some of the clinical manifestations and biochemical findings. However, recent reports suggest that recurrent admi...

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Detalhes bibliográficos
Publicado no:Mol Genet Metab Rep
Main Authors: Tsukimura, Takahiro, Tayama, Yuya, Shiga, Tomoko, Hirai, Kanako, Togawa, Tadayasu, Sakuraba, Hitoshi
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7548986/
https://ncbi.nlm.nih.gov/pubmed/33072516
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgmr.2020.100650
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