Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathySusan Sparks, Marjan Huizing, William A. Gahl et al.|Glycobiology|2005Cited by 46
Allele‐specific silencing of the dominant disease allele in sialuria by RNA interferenceRiko Klootwijk, Marjan Huizing, Paul J.M. Savelkoul et al.|The FASEB Journal|2008Cited by 17
Normal sialylation of serum N-linked and O-GalNAc-linked glycans in hereditary inclusion-body myopathyPaul J.M. Savelkoul, Marjan Huizing, Irini Manoli et al.|Molecular Genetics and Metabolism|2006Cited by 16
Single nucleotide polymorphisms in the dystroglycan gene do not correlate with disease severity in hereditary inclusion body myopathyEmily Gottlieb, Marjan Huizing, Donna M. Krasnewich et al.|Molecular Genetics and Metabolism|2005Cited by 6