Management of pediatric patients with inborn errors of metabolism.
Studies in genetic disorders of fatty-acid metabolism.
RECENT PUBLICATIONS
Kakkis ED, Muenzer J, tiller GE, Waber LJ, Belmont J, Passage M, Izykowski B, Phillips J, Doroshow R, Walot I, Hoft R, Neufeld EF., "Enzyme replacement therapy in Mucopolysaccharidosis I." New Eng J Med, 344:182-188, 2001
Praphanphoj V, Boydjiev SA, Waber LJ, Brusilow SW, Geraghty MT., "Three cases of intravenous sodium benzoate and sodium phenylacetate toxicity occurring in the treatment of acute hyperammonemia." J Inherit Metab Dis, 23:129-136, 2000
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