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Journal of Inherited Metabolic Disease
|
March 30, 2011
Biomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodies
Johannes 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 shortage
Gabor 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 document
Marieke Biegstraaten, Reynir Arngrímsson, Frederic Barbey, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 63) with videos related to
Sort By:
Page
of 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 inhibodies
Johannes 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 shortage
Gabor 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 document
Marieke Biegstraaten, Reynir Arngrímsson, Frederic Barbey, et al.
Page
of 7