Dysfunction of endocytic and autophagic pathways in a lysosomal storage diseaseTokiko Fukuda, Nina Raben, Kristien J.M. Zaal et al.|Annals of Neurology|2006Cited by 300
Autophagy and Mistargeting of Therapeutic Enzyme in Skeletal Muscle in Pompe DiseaseTokiko Fukuda, Nina Raben, Ashley Roberts et al.|Molecular Therapy|2006Cited by 186
Replacing acid α-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibersNina Raben, Paul H. Plötz, Tokiko Fukuda et al.|Molecular Therapy|2004Cited by 138
Autophagy and Lysosomes in Pompe DiseaseTokiko Fukuda, Nina Raben, Ashley Roberts et al.|Autophagy|2006Cited by 118
Acid alpha-glucosidase deficiency (Pompe disease)Tokiko Fukuda, Nina Raben, Ashley Roberts et al.|Current Neurology and Neuroscience Reports|2007Cited by 52