Enzyme replacement therapy for late-onset Pompe disease

Author:

Sharma Reena1,Hughes Derralynn2,Ramaswami Uma3,Cole Duncan4,Roberts Mark1,Hendriksz Christian J1,Stepien Karolina M1,Krishan Ashma5,Jahnke Nikki6

Affiliation:

1. Salford Royal NHS Foundation Trust; Adult Inherited Metabolic Disorders, The Mark Holland Metabolic Unit; Ladywell NW2 - 2nd Floor Salford UK M6 8HD

2. Royal Free Hospital; Department of Haematology; London UK

3. Royal Free Hospital; Lysosomal Unit; London UK

4. Cardiff University School of Medicine; Institute of Molecular & Experimental Medicine; UHW Main Building Heath Park Cardiff UK CF14 4XN

5. University of Liverpool, Alder Hey Children's NHS Foundation Trust; Department of Women's and Children's Health; Eaton Road Liverpool Merseyside UK L12 2AP

6. University of Liverpool; Department of Women's and Children's Health; Alder Hey Children's NHS Foundation Trust Eaton Road Liverpool UK L12 2AP

Publisher

Wiley

Subject

Pharmacology (medical)

Reference24 articles.

1. A 49-year-old woman with progressive shortness of breath;Amato;Neurology,2011

2. Frequency of glycogen storage disease type II in the Netherlands: implications for diagnosis and genetic counselling;Ausems;European Journal of Human Genetics,1999

3. Pearls & Oy-sters: clues to the diagnosis of adult-onset acid maltase deficiency;Beltran Papsdorf;Neurology,2014

4. A coefficient of agreement for nominal scales;Cohen;Educational and Psychological Measurement,1960

5. Deeks J Higgins J Altman D editor(s) Chapter 9: Analysing data and undertaking meta-analysis. In: Higgins JP, Green S, editor(s). Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 (updated March 2011). The Cochrane Collaboration, 2011 Available from handbook.cochrane.org

Cited by 1 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. Enzyme replacement therapy for late-onset Pompe disease;Cochrane Database of Systematic Reviews;2023-12-12

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