Showing results (101-110 of 232) with videos related to

Sort By:
Pageof 24
Pediatric Research|September 7, 2004
Disease-specific markers for the mucopolysaccharidosesMaria Fuller, Tina Rozaklis, Steven L Ramsay, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|August 23, 2011
Incidence and predictors of anti-bradycardia pacing in patients with Anderson-Fabry diseaseConstantinos O'Mahony, Caroline Coats, Monserrat Cardona, et al.
Journal of Inherited Metabolic Disease|November 16, 2012
Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytesDerek G Burke, Ahad A Rahim, Simon N Waddington, et al.
Molecular Genetics and Metabolism Reports|March 4, 2016
Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysisMichael Beck, Derralynn Hughes, Christoph Kampmann, et al.
Molecular Genetics and Metabolism|September 12, 2016
Home infusion of intravenous velaglucerase alfa: Experience from pooled clinical studies in 104 patients with type 1 Gaucher diseaseDeborah Elstein, T Andrew Burrow, Joel Charrow, et al.
British Journal of Haematology|March 22, 2003
Cytogenetics of multiple myeloma: interpretation of fluorescence in situ hybridization resultsChristine J Harrison, Helen Mazzullo, Kan L Cheung, et al.
Clinical Chemistry and Laboratory Medicine|August 24, 2022
Free urinary sialic acid levels may be elevated in patients with pneumococcal sepsisSarah E Donoghue, Oliver Heath, James Pitt, et al.
Biodrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy|February 5, 2005
Laronidase treatment of mucopolysaccharidosis IEd J Wraith, John J Hopwood, Maria Fuller, et al.
Journal of Inherited Metabolic Disease|November 11, 2019
Expanding the clinical utility of glucosylsphingosine for Gaucher diseaseJennifer T Saville, Belinda K McDermott, Sharon J Chin, et al.
Blood Cells, Molecules & Diseases|May 7, 2013
Transgenic mice expressing human glucocerebrosidase variants: utility for the study of Gaucher diseaseAngela Sanders, Harmony Hemmelgarn, Heather L Melrose, et al.
Pageof 24