共 18 条
- [1] Chou JY(2002)Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex Curr Mol Med 2 121–143-676
- [2] Matern D(2006)A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease J Pediatr 148 671-97
- [3] Mansfield BC(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 10 467–471-undefined
- [4] Kishnani PS(2005)The natural course of non-classic Pompe’s disease: a review of 225 published cases J Neurol 252 875–884-undefined
- [5] Hwu WL(2006)Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease J Pediatr 149 89-undefined
- [6] Mandel H(2004)Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk Pediatrics 113 e448–e457-undefined
- [7] Ausems MG(undefined)undefined undefined undefined undefined-undefined
- [8] ten Berg K(undefined)undefined undefined undefined undefined-undefined
- [9] Beemer FA(undefined)undefined undefined undefined undefined-undefined
- [10] Winkel LP(undefined)undefined undefined undefined undefined-undefined