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Glycobiology
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January 14, 2005
Lysosomal metabolism of glycoproteins
Bryan Winchester
Journal of Inherited Metabolic Disease
|
April 9, 2014
Lysosomal diseases: diagnostic update
Bryan Winchester
European Journal of Human Genetics : EJHG
|
September 22, 2011
Clinical utility gene card for: Fabry disease
Andreas Gal, Michael Beck, Bryan Winchester
FEBS Letters
|
April 12, 2002
Synthesis of novel internal standards for the quantitative determination of plasma ceramide trihexoside in Fabry disease by tandem mass spectrometry
Kevin Mills, Andrew Johnson, Bryan Winchester
Journal of Inherited Metabolic Disease
|
January 14, 2011
Toward a consensus in the laboratory diagnostics of Fabry disease - recommendations of a European expert group
Andreas Gal, Derralynn A Hughes, Bryan Winchester
Rapid Communications in Mass Spectrometry : RCM
|
May 24, 2005
The synthesis of internal standards for the quantitative determination of sphingolipids by tandem mass spectrometry
Kevin Mills, Simon Eaton, Victoria Ledger, et al.
Molecular Genetics and Metabolism
|
June 5, 2012
Biomarkers for the mucopolysaccharidoses: discovery and clinical utility
Lorne A Clarke, Bryan Winchester, Roberto Giugliani, et al.
European Journal of Pediatrics
|
July 10, 2004
Monitoring the clinical and biochemical response to enzyme replacement therapy in three children with Fabry disease
Kevin Mills, Ashok Vellodi, Peter Morris, et al.
American Journal of Human Genetics
|
March 4, 2008
Human RFT1 deficiency leads to a disorder of N-linked glycosylation
Micha A Haeuptle, François M Pujol, Christine Neupert, et al.
Chembiochem : a European Journal of Chemical Biology
|
April 1, 2005
Potent and selective inhibition of class II alpha-D-mannosidase activity by a bicyclic sulfonium salt
Aloysius Siriwardena, Heather Strachan, Samer El-Daher, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Glycobiology
|
January 14, 2005
Lysosomal metabolism of glycoproteins
Bryan Winchester
Journal of Inherited Metabolic Disease
|
April 9, 2014
Lysosomal diseases: diagnostic update
Bryan Winchester
European Journal of Human Genetics : EJHG
|
September 22, 2011
Clinical utility gene card for: Fabry disease
Andreas Gal, Michael Beck, Bryan Winchester
FEBS Letters
|
April 12, 2002
Synthesis of novel internal standards for the quantitative determination of plasma ceramide trihexoside in Fabry disease by tandem mass spectrometry
Kevin Mills, Andrew Johnson, Bryan Winchester
Journal of Inherited Metabolic Disease
|
January 14, 2011
Toward a consensus in the laboratory diagnostics of Fabry disease - recommendations of a European expert group
Andreas Gal, Derralynn A Hughes, Bryan Winchester
Rapid Communications in Mass Spectrometry : RCM
|
May 24, 2005
The synthesis of internal standards for the quantitative determination of sphingolipids by tandem mass spectrometry
Kevin Mills, Simon Eaton, Victoria Ledger, et al.
Molecular Genetics and Metabolism
|
June 5, 2012
Biomarkers for the mucopolysaccharidoses: discovery and clinical utility
Lorne A Clarke, Bryan Winchester, Roberto Giugliani, et al.
European Journal of Pediatrics
|
July 10, 2004
Monitoring the clinical and biochemical response to enzyme replacement therapy in three children with Fabry disease
Kevin Mills, Ashok Vellodi, Peter Morris, et al.
American Journal of Human Genetics
|
March 4, 2008
Human RFT1 deficiency leads to a disorder of N-linked glycosylation
Micha A Haeuptle, François M Pujol, Christine Neupert, et al.
Chembiochem : a European Journal of Chemical Biology
|
April 1, 2005
Potent and selective inhibition of class II alpha-D-mannosidase activity by a bicyclic sulfonium salt
Aloysius Siriwardena, Heather Strachan, Samer El-Daher, et al.
Page
of 3