Biomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodies

A biomarker is an analyte indicating the presence of a biological process linked to the clinical manifestations and outcome of a particular disease. In the case of lysosomal storage disorders (LSDs), primary and secondary accumulating metabolites or proteins specifically secreted by storage cells ar...

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Veröffentlicht in:	Journal of inherited metabolic disease 2011-06, Vol.34 (3), p.605-619
Hauptverfasser:	Aerts, Johannes M. F. G., Kallemeijn, Wouter W., Wegdam, Wouter, Joao Ferraz, Maria, van Breemen, Marielle J., Dekker, Nick, Kramer, Gertjan, Poorthuis, Ben J., Groener, Johanna E. M., Cox-Brinkman, Josanne, Rombach, Saskia M., Hollak, Carla E. M., Linthorst, Gabor E., Witte, Martin D., Gold, Henrik, van der Marel, Gijs A., Overkleeft, Herman S., Boot, Rolf G.
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Antibodies Biochemistry Biological and medical sciences Biomarkers - analysis Biomarkers - metabolism Enzyme Replacement Therapy Fabry Disease - diagnosis Fabry Disease - metabolism Fabry Disease - pathology Fabry Disease - therapy Gaucher Disease - diagnosis Gaucher Disease - metabolism Gaucher Disease - pathology Gaucher Disease - therapy Human Genetics Humans Internal Medicine Lipids - analysis Lysosomal Storage Diseases - diagnosis Lysosomal Storage Diseases - metabolism Lysosomal Storage Diseases - pathology Lysosomal Storage Diseases - therapy Medical genetics Medical sciences Medicine Medicine & Public Health Metabolic Diseases Models, Molecular Pediatrics Proteins - analysis Proteins - metabolism SSIEM Symposium 2010
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