Recombinant human acid α-glucosidase
Major clinical benefits in infantile-onset Pompe disease
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- A novel CD71 Centyrin:Gys1 siRNA conjugate reduces glycogen synthesis and glycogen levels in a mouse model of Pompe disease, Molecular Therapy, 33, 1, (235-248), (2025).https://doi.org/10.1016/j.ymthe.2024.11.033
- Dose-intensive therapy (DIT) for infantile Pompe disease: A pilot study, Molecular Genetics and Metabolism Reports, 42, (101179), (2025).https://doi.org/10.1016/j.ymgmr.2024.101179
- Levels Above Lower Motor Neuron to Neuromuscular Junction, Volpe's Neurology of the Newborn, (1039-1073.e12), (2025).https://doi.org/10.1016/B978-0-443-10513-5.00036-X
- Importance of early treatment and quantitative evaluation of enzyme replacement therapy for Pompe disease: alglucosidase alfa post-marketing surveillance additional analysisポンペ病酵素補充療法有効性評価と治療開始時期:アルグルコシダーゼ アルファ特定使用成績調査追加解析, Rinsho Shinkeigaku, 64, 12, (866-877), (2024).https://doi.org/10.5692/clinicalneurol.cn-001894
- Effectiveness of Respiratory Muscle Training in Pompe Disease: A Systematic Review and Meta-Analysis, Children, 11, 10, (1209), (2024).https://doi.org/10.3390/children11101209
- Efficacy and safety of enzyme replacement therapy with alglucosidase alfa for the treatment of patients with infantile-onset Pompe disease: a systematic review and metanalysis, Frontiers in Pediatrics, 12, (2024).https://doi.org/10.3389/fped.2024.1310317
- An updated management approach of Pompe disease patients with high-sustained anti-rhGAA IgG antibody titers: experience with bortezomib-based immunomodulation, Frontiers in Immunology, 15, (2024).https://doi.org/10.3389/fimmu.2024.1360369
- Optimizing treatment outcomes: immune tolerance induction in Pompe disease patients undergoing enzyme replacement therapy, Frontiers in Immunology, 15, (2024).https://doi.org/10.3389/fimmu.2024.1336599
- Editorial: Inborn errors of carbohydrate metabolism, Frontiers in Genetics, 15, (2024).https://doi.org/10.3389/fgene.2024.1430414
- The Importance of Early Treatment of Inherited Neuromuscular Conditions, Journal of Neuromuscular Diseases, 11, 2, (253-274), (2024).https://doi.org/10.3233/JND-230189
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