Glycogen storage disease manifested as gout and myopathy: three case reports and literature review
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Rheumatology
Link
http://link.springer.com/content/pdf/10.1007/s10067-007-0798-4.pdf
Reference6 articles.
1. Chou JY, Matern D, Mansfield BC et al (2002) Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex. Curr Mol Med 2(2):121–143
2. Kishnani PS, Hwu WL, Mandel H et al (2006) A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J Pediatr 148(5):671–676
3. Ausems MG, ten Berg K, Beemer FA (2000) Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families. Neuromuscul Disord 10(7):467–471
4. Winkel LP, Hagemans ML, van Doorn PA (2005) The natural course of non-classic Pompe’s disease: a review of 225 published cases. J Neurol 252(8):875–884
5. Kishnani PS, Nicolino M, Voit T et al (2006) Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease. J Pediatr 149(1):89–97
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