Fabry Disease: Preclinical Studies Demonstrate the Effectiveness of α-Galactosidase A Replacement in Enzyme-Deficient MiceYiannis A. Ioannou, Robert J. Desnick, Ken M. Zeidner et al.|The American Journal of Human Genetics|2001Cited by 201
Human α-galactosidase A: glycosylation site 3 is essential for enzyme solubilityYiannis A. Ioannou, Robert J. Desnick, Ken M. Zeidner et al.|Biochemical Journal|1998Cited by 105
Correction of Enzymatic and Lysosomal Storage Defects in Fabry Mice by Adenovirus-Mediated Gene TransferR. J. Ziegler, Robert J. Desnick, Chang Li et al.|Human Gene Therapy|1999Cited by 97
Quantitative Determination of Globotriaosylceramide by Immunodetection of Glycolipid-Bound Recombinant Verotoxin B SubunitKen M. Zeidner, Yiannis A. Ioannou, Robert J. Desnick|Analytical Biochemistry|1999Cited by 49
Murine α-N-Acetylgalactosaminidase: Isolation and Expression of a Full-Length cDNA and Genomic Organization: Further Evidence of an α-Galactosidase Gene FamilyAnne M. Wang, Robert J. Desnick, Yiannis A. Ioannou et al.|Molecular Genetics and Metabolism|1998Cited by 9