Colleen Bindloss

Determination of Acid α-Glucosidase Protein: Evaluation as a Screening Marker for Pompe Disease and Other Lysosomal Storage Disorders

Kandiah Umapathysivam, Alison M. Whittle, Enzo Ranieri et al. · Clinical Chemistry · 2000 · 61 citations · Full text

Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases

Steven L. Ramsay, Irène Maire, Colleen Bindloss et al. · Molecular Genetics and Metabolism · 2004 · 58 citations

Lysosomal Storage Diseases, Amniotic Fluid, Biochemistry +13

Correlation among Genotype, Phenotype, and Biochemical Markers in Gaucher Disease: Implications for the Prediction of Disease Severity

Phillip D. Whitfield, Paul V. Nelson, P. Sharp et al. · Molecular Genetics and Metabolism · 2002 · 50 citations

Biochemical Markers, Gaucher Disease, Disease Severity +9

Saposins A, B, C, and D in Plasma of Patients with Lysosomal Storage Disorders

Melissa H. Chang, Colleen Bindloss, Gregory A. Grabowski et al. · Clinical Chemistry · 2000 · 35 citations · Full text

Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the <i>N</i>-acetylgalactosamine 4-sulphatase protein

Doug A. Brooks, D A Robertson, Colleen Bindloss et al. · Biochemical Journal · 1995 · 33 citations · Full text

Aldo-keto Reductase, Amino Acids, Pathology +17