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Gabor E Linthorst

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Journal of Inherited Metabolic Disease|March 30, 2011
Biomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodiesJohannes M F G Aerts, Wouter W Kallemeijn, Wouter Wegdam, et al.
JIMD Reports|February 23, 2013
Recommendations on reintroduction of agalsidase Beta for patients with fabry disease in europe, following a period of shortageGabor E Linthorst, Alessandro P Burlina, Franco Cecchi, et al.
Orphanet Journal of Rare Diseases|April 18, 2015
Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus documentMarieke Biegstraaten, Reynir Arngrímsson, Frederic Barbey, et al.
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Showing results (61-70 of 63) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 63 results.
Journal of Inherited Metabolic Disease|March 30, 2011
Biomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodiesJohannes M F G Aerts, Wouter W Kallemeijn, Wouter Wegdam, et al.
JIMD Reports|February 23, 2013
Recommendations on reintroduction of agalsidase Beta for patients with fabry disease in europe, following a period of shortageGabor E Linthorst, Alessandro P Burlina, Franco Cecchi, et al.
Orphanet Journal of Rare Diseases|April 18, 2015
Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus documentMarieke Biegstraaten, Reynir Arngrímsson, Frederic Barbey, et al.
Pageof 7