Receptor-Mediated Uptake of Acid α-Glucosidase Corrects Lysosomal Glycogen Storage in Cultured Skeletal Muscle-Reference-Cited by-同舟云学术

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Receptor-Mediated Uptake of Acid α-Glucosidase Corrects Lysosomal Glycogen Storage in Cultured Skeletal Muscle

Published:1988-07 Issue:1 Volume:24 Page:90-94
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Van Der Ploeg Ans T,B. Loonen M Christa,Bolhuis Piet A,Busch Herman M F,Reuser Arnold J J,Galjaard Hans

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Cited by 40 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pompe disease, a rare condition in two patients, case reports;JAP Academy Journal;2023-01-27

2. Effect of alglucosidase alfa dosage on survival and walking ability in patients with classic infantile Pompe disease: a multicentre observational cohort study from the European Pompe Consortium;The Lancet Child & Adolescent Health;2022-01

3. Endolysosomal N-glycan processing is critical to attain the most active form of the enzyme acid alpha-glucosidase;Journal of Biological Chemistry;2021-01

4. Effects of higher and more frequent dosing of alglucosidase alfa and immunomodulation on long‐term clinical outcome of classic infantile Pompe patients;Journal of Inherited Metabolic Disease;2020-07-13

5. Challenges in treating Pompe disease: an industry perspective;Annals of Translational Medicine;2019-07

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