Creating genetics-based infusion centers: a case study of two models
Dawn J. Laney(Emory University), Paul M. Fernhoff, William J. Rhead(Children's Hospital of Wisconsin), Amy White
Cited by 2
Related Papers
Survival after Treatment with Phenylacetate and Benzoate for Urea-Cycle Disorders
|New England Journal of Medicine|2007|357
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation
|Proceedings of the National Academy of Sciences|1998|254
‘Classical’ organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: Long‐term outcome and effects of expanded newborn screening using tandem mass spectrometry
|Journal of Inherited Metabolic Disease|2006|247
Phenylketonuria in adulthood: A collaborative study
|Journal of Inherited Metabolic Disease|2002|215
Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease
|Genetics in Medicine|2012|212