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Human Mutation|July 19, 2002
The molecular basis of cystathionine beta-synthase deficiency in Australian patients: genotype-phenotype correlations and response to treatmentMette Gaustadnes, Bridget Wilcken, Jana Oliveriusova, et al.European Journal of Pediatrics|November 18, 2003
Ethical issues in newborn screening and the impact of new technologiesBridget WilckenJournal of Inherited Metabolic Disease|January 6, 2010
Fatty acid oxidation disorders: outcome and long-term prognosisBridget WilckenPathology|December 27, 2011
Screening for disease in the newborn: the evidence base for blood-spot screeningBridget WilckenMolecular Genetics and Metabolism|March 31, 2004
Problems in the management of urea cycle disordersBridget WilckenAnnals of the Academy of Medicine, Singapore|November 12, 2009
Disorders of the carnitine cycle and detection by newborn screeningBridget WilckenJournal of Inherited Metabolic Disease|April 19, 2011
Newborn screening: how are we travelling, and where should we be going?Bridget WilckenThe Southeast Asian Journal of Tropical Medicine and Public Health|May 24, 2005
An introduction to nutritional treatment in inborn errors of metabolism--different disorders, different approachesBridget WilckenJournal of Inherited Metabolic Disease|June 10, 2006
Mini-symposium: newborn screening for inborn errors of metabolism--clinical effectivenessBridget WilckenPageof 12