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International Journal of Cardiology|June 24, 2008
Onset and progression of the Anderson-Fabry disease related cardiomyopathyChristoph Kampmann, Ales Linhart, Frank Baehner, et al.Journal of Inherited Metabolic Disease|September 15, 2006
Critical assessment of chitotriosidase analysis in the rational laboratory diagnosis of children with Gaucher disease and Niemann-Pick disease type A/B and CMarkus Ries, Ellen Schaefer, Till Lührs, et al.Progress in Retinal and Eye Research|August 2, 2003
Vitamin A metabolism in the retinal pigment epithelium: genes, mutations, and diseasesDebra A Thompson, Andreas GalDevelopments in Ophthalmology|July 25, 2003
Genetic defects in vitamin A metabolism of the retinal pigment epitheliumDebra A Thompson, Andreas GalRapid Communications in Mass Spectrometry : RCM|May 24, 2005
The synthesis of internal standards for the quantitative determination of sphingolipids by tandem mass spectrometryKevin Mills, Simon Eaton, Victoria Ledger, et al.Molecular Vision|November 17, 2005
Protocadherin-21 (PCDH21), a candidate gene for human retinal dystrophiesHanno Bolz, Inga Ebermann, Andreas GalThe Journal of Biological Chemistry|December 22, 2004
AlphaPIX associates with calpain 4, the small subunit of calpain, and has a dual role in integrin-mediated cell spreadingGeorg Rosenberger, Andreas Gal, Kerstin KutscheMolecular Genetics and Metabolism|June 5, 2012
Biomarkers for the mucopolysaccharidoses: discovery and clinical utilityLorne A Clarke, Bryan Winchester, Roberto Giugliani, et al.Current Pharmaceutical Biotechnology|January 18, 2011
Mucopolysaccharidosis Type II (Hunter Syndrome): clinical picture and treatmentMichael BeckPageof 31