Suppression of autophagy permits successful enzyme replacement therapy in a lysosomal storage disorder—murine Pompe diseaseNina Raben, Paul H. Plötz, Kanneboyina Nagaraju et al.|Autophagy|2010Cited by 160
Murine muscle cell models for Pompe disease and their use in studying therapeutic approachesShoichi Takikita, Paul H. Plötz, Kristien J.M. Zaal et al.|Molecular Genetics and Metabolism|2009Cited by 39
The values and limits of an in vitro model of Pompe disease: The best laid schemes o’ mice an’ men ……..<sup>†</sup>Shoichi Takikita, Paul H. Plötz, Nina Raben et al.|Autophagy|2009Cited by 16