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Archives of Disease in Childhood|February 1, 1997
Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centresA Vellodi, E P Young, A Cooper, et al.
Simulation in Healthcare : Journal of the Society for Simulation in Healthcare|September 10, 2020
The Impact of a Comprehensive Simulation-Based Training and Certification Program on Resident Central Venous Catheter Complication RatesJonathan Day, Zachary B Winchester, Cassandra A Cairns, et al.
Clinical Chemistry|February 5, 2000
Saposins A, B, C, and D in plasma of patients with lysosomal storage disordersM H Chang, C A Bindloss, G A Grabowski, et al.
Molecular Genetics and Metabolism|April 7, 1999
A rapid fluorogenic palmitoyl-protein thioesterase assay: pre- and postnatal diagnosis of INCLO P van Diggelen, J L Keulemans, B Winchester, et al.
The British Journal of Dermatology|April 1, 1994
Neutral lipid storage disease. Case report and lipid studiesM R Judge, D J Atherton, R Salvayre, et al.
Journal of Inherited Metabolic Disease|January 24, 2002
Anderson-Fabry disease: clinical manifestations of disease in female heterozygotesC Whybra, C Kampmann, I Willers, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease type A (MPS IIIA)E A Karpova, Voznyi YaV, J L Keulemans, et al.
The Journal of Biological Chemistry|April 25, 1990
Cloning and expression of peptide-N4-(N-acetyl-beta-D-glucosaminyl)asparagine amidase F in Escherichia coliG D Barsomian, T L Johnson, M Borowski, et al.
Clinical Immunology and Immunopathology|May 1, 1985
Complement activation in type 1 human diabetesJ S Sundsmo, R A Papin, L Wood, et al.
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