Publications by authors named "Annette S Feigenbaum"

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Aicardi-Goutières syndrome may present with positive newborn screen for X-linked adrenoleukodystrophy.
Christina G Tise, Jose Andres Morales, Ariel S Lee, Frances Velez-Bartolomei, Brendan J Floyd, Annette S Feigenbaum

Am J Med Genet A· June 2021

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Design and implementation of the first randomized controlled trial of coenzyme CoQ₁₀ in children with primary mitochondrial diseases.
Peter W Stacpoole, Ton J deGrauw, Annette S Feigenbaum, Charles Hoppel, Douglas S Kerr

Mitochondrion· November 2012

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MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation.
Barbara S Connolly, Annette S J Feigenbaum, Brian H Robinson, Anne I Dipchand, David K Simon

Biochem Biophys Res Commun· November 2010

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IDH2 mutations in patients with D-2-hydroxyglutaric aciduria.
Martijn Kranendijk, Eduard A Struys, Emile van Schaftingen, K Michael Gibson, Warsha A Kanhai, Annette S Feigenbaum

Science· October 2010

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Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutations.
Klaus G E Werner, Chantal F Morel, Adam Kirton, Susanne M Benseler, John M Shoffner, Annette S J Feigenbaum

Pediatr Neurol· July 2009

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Efficacy of sapropterin dihydrochloride (tetrahydrobiopterin, 6R-BH4) for reduction of phenylalanine concentration in patients with phenylketonuria: a phase III randomised placebo-controlled study.
Harvey L Levy, Andrzej Milanowski, Anupam Chakrapani, Maureen Cleary, Philip Lee, Annette S Feigenbaum

Lancet· August 2007

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