Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study-Reference-Cited by-同舟云学术

Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study

Published:2012 Issue:1 Volume:7 Page:88
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet Journal of Rare Diseases

Author:

van der Beek Nadine AME,de Vries Juna M,Hagemans Marloes LC,Hop Wim CJ,Kroos Marian A,Wokke John HJ,de Visser Marianne,van Engelen Baziel GM,Kuks Jan BM,van der Kooi Anneke J,Notermans Nicolette C,Faber Karin G,Verschuuren Jan JGM,Reuser Arnold JJ,van der Ploeg Ans T,van Doorn Pieter A

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Reference32 articles.

1. The spectrum and diagnosis of acid maltase deficiency

2. Pompe's disease

3. Chinese hamster ovary cell-derived recombinant human acid α-glucosidase in infantile-onset Pompe disease

4. Recombinant human acid -glucosidase: Major clinical benefits in infantile-onset Pompe disease

5. Recombinant human α-glucosidase from rabbit milk in Pompe patients

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