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Molecular Genetics and Metabolism|January 7, 2024
Evaluating change in diet with pegvaliase treatment in adults with phenylketonuria: Analysis of phase 3 clinical trial dataFran Rohr, Barbara Burton, Anne Dee, et al.The British Journal of Nutrition|October 19, 2022
Left ventricular diastolic abnormalities in vegetarians compared with non-vegetariansPadmini Varadarajan, Ramdas G Pai, Gary E Fraser, et al.Journal of Inherited Metabolic Disease|September 5, 2020
Effects of triheptanoin (UX007) in patients with long-chain fatty acid oxidation disorders: Results from an open-label, long-term extension studyJerry Vockley, Barbara Burton, Gerard Berry, et al.European Journal of Pediatrics|November 1, 2011
The role of enzyme replacement therapy in severe Hunter syndrome-an expert panel consensusJoseph Muenzer, Olaf Bodamer, Barbara Burton, et al.Molecular Genetics and Metabolism|February 6, 2014
Liver transplantation for pediatric metabolic diseaseGeorge Mazariegos, Benjamin Shneider, Barbara Burton, et al.Molecular Genetics and Metabolism|January 23, 2009
A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiencyGeorgianne L Arnold, Johan Van Hove, Debra Freedenberg, et al.Journal of Inherited Metabolic Disease|May 10, 2014
Efficacy and safety of enzyme replacement therapy with BMN 110 (elosulfase alfa) for Morquio A syndrome (mucopolysaccharidosis IVA): a phase 3 randomised placebo-controlled studyChristian J Hendriksz, Barbara Burton, Thomas R Fleming, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 17, 2007
Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiencyDevin Oglesbee, Miao He, Nilanjana Majumder, et al.Journal of Inherited Metabolic Disease|February 12, 2019
Results from a 78-week, single-arm, open-label phase 2 study to evaluate UX007 in pediatric and adult patients with severe long-chain fatty acid oxidation disorders (LC-FAOD)Jerry Vockley, Barbara Burton, Gerard T Berry, et al.Molecular Genetics and Metabolism|December 25, 2007
A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiencyGeorgianne L Arnold, Dwight D Koeberl, Dietrich Matern, et al.Pageof 4