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Featured Articles

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  Alternative Therapies in Phenylketonuria

  Susan Thompson BSc, AdvAPD,Frances J. Rohr MS, RD

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  Effect of Feeding, Exercise, and Genotype on Plasma 3-Hydroxyacylcarnitines in Children With LCHAD Deficiency

  Melanie B. Gillingham PhD, RD,Dietrich Matern MD,Cary O. Harding MD

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  Emergency Management of Inherited Metabolic Disorders

  Shideh Mofidi MS, RD, CSP,David Kronn MD

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  Medical Food for Treatment of Inborn Errors of Metabolism and State Legislative Mandates

  Kathleen Huntington MS, RD, LD,Neil R. M. Buist MB, ChB, FRCPE, DCH

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  Network Phenylketonuria Conference: An Effective Tool for Facilitating Adherence to Diet Therapy in Individuals With Phenylketonuria

  Cynthia L. Freehauf MS, RN, CGC,Laurie Bernstein MS, RD, FADA,Kiersten Amos LLB,Katherine Isacks MPS, RD,Dexiang Gao PhD,Janet A. Thomas MD

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  Normal Fatty Acid Concentrations in Young Children With Phenylketonuria

  Stacey M. LaVoie MS, RD,Cary O. Harding MD,Melanie B. Gillingham PhD, RD

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  Nutritional Management of Methylmalonic and Propionic Acidemia: Three Peritransplant Patients

  Bridget A. Reineking MS, RD, CD,Antoinette C. Maraglino MS, RD, LDN,Keiko Ueda MPH, RD, LDN

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  Tandem Mass Spectrometry Newborn Screening and Its Impact on Inborn Errors of Metabolism

  Dianne M. Frazier PhD, MPH, RD, LDN

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  The Diagnosis and Management of a Female With Mild Citrullinemia and Undetectable Argininosuccinate Synthetase Activity in Fibroblasts

  Surekha Pendyal MSc, MEd, RD,Joseph Muenzer MD, PhD