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Pediatrics|December 5, 2003
The Maternal Phenylketonuria Project: a summary of progress and challenges for the futureJoe T R ClarkeDrugs|December 8, 2007
Treatment of lysosomal storage disorders : progress with enzyme replacement therapyMarianne Rohrbach, Joe T R ClarkeJournal of Inherited Metabolic Disease|June 28, 2006
Ornithine transcarbamoylase deficiency presenting with acute liver failureAhlam Mustafa, Joe T R ClarkeIrish Medical Journal|March 1, 1997
General practitioners knowledge of and attitudes to the use of seat belts in pregnancyC WallaceRadiography (London, England : 1995)|July 8, 2023
An exploration of simulation-based education from other health professionals, to create an informed and effective simulation delivery in a new diagnostic radiography programmeC WallaceExpert Opinion on Biological Therapy|April 17, 2009
The use of agalsidase alfa enzyme replacement therapy in the treatment of Fabry diseaseChantal F Morel, Joe T R ClarkeCytogenetics and Cell Genetics|January 1, 1977
Chromosome analysis in the Kruger National Park: the chromosomes of the bushbuck (Tragelaphus scriptus)C WallaceNursing Standard (Royal College of Nursing (Great Britain) : 1987)|May 14, 2010
Integrated assessment of older adults who misuse alcoholC WallaceMolecular Neurobiology|August 4, 2005
Enzyme replacement therapy of Fabry diseaseJoe T R Clarke, R Mark IwanochkoPageof 157