Recommendations for the nutrition management of phenylalanine hydroxylase deficiency

Insurance coverage of medical foods for treatment of inherited metabolic disorders

(2013) Susan A. Berry et al.   GENETICS IN MEDICINE

Large Neutral Amino Acid Supplementation Increases Melatonin Synthesis in Phenylketonuria: A New Biomarker

(2012) Shoji Yano et al.   JOURNAL OF PEDIATRICS

The use of parenteral nutrition for the management of PKU patient undergoing chemotherapy for lymphoma: A case report

(2012) R. Salvarinova-Zivkovic et al.   MOLECULAR GENETICS AND METABOLISM

Recommendations for the use of sapropterin in phenylketonuria

(2012) Amy Cunningham et al.   MOLECULAR GENETICS AND METABOLISM

Long-term treatment with tetrahydrobiopterin in phenylketonuria: Treatment strategies and prediction of long-term responders

(2012) Julia B. Hennermann et al.   MOLECULAR GENETICS AND METABOLISM

Positive effect of a simplified diet on blood phenylalanine control in different phenylketonuria variants, characterized by newborn BH4 loading test and PAH analysis

(2012) M. Zimmermann et al.   MOLECULAR GENETICS AND METABOLISM

Dietary treatment in phenylketonuria does not lead to increased risk of obesity or metabolic syndrome

(2012) Júlio C. Rocha et al.   MOLECULAR GENETICS AND METABOLISM

High prevalence of overweight and obesity in females with phenylketonuria

(2012) Lindsay C. Burrage et al.   MOLECULAR GENETICS AND METABOLISM

Food Products Made with Glycomacropeptide, a Low-Phenylalanine Whey Protein, Provide a New Alternative to Amino Acid–Based Medical Foods for Nutrition Management of Phenylketonuria

(2012) Sandra C. van Calcar et al.   Journal of the Academy of Nutrition and Dietetics

Bridging evidence and consensus methodology for inherited metabolic disorders: creating nutrition guidelines

(2011) Rani H. Singh et al.   JOURNAL OF EVALUATION IN CLINICAL PRACTICE

Impact of Metabolic Control on Bone Quality in Phenylketonuria and Mild Hyperphenylalaninemia

(2011) Francesco Porta et al.   JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION

Using change in plasma phenylalanine concentrations and ability to liberalize diet to classify responsiveness to tetrahydrobiopterin therapy in patients with phenylketonuria

(2011) Rani H. Singh et al.   MOLECULAR GENETICS AND METABOLISM

Vitamin B12 deficiency and phenylketonuria

(2011) John H. Walter   MOLECULAR GENETICS AND METABOLISM

Non-PKU mild hyperphenylalaninemia (MHP) — The dilemma

(2011) W.B. Hanley   MOLECULAR GENETICS AND METABOLISM

Diagnosis, classification, and genetics of phenylketonuria and tetrahydrobiopterin (BH4) deficiencies

(2011) Nenad Blau et al.   MOLECULAR GENETICS AND METABOLISM

The Use of Prealbumin Concentration as a Biomarker of Nutritional Status in Treated Phenylketonuric Patients

(2010) Júlio César Rocha et al.   ANNALS OF NUTRITION AND METABOLISM

Breakfast with glycomacropeptide compared with amino acids suppresses plasma ghrelin levels in individuals with phenylketonuria

(2010) Erin L. MacLeod et al.   MOLECULAR GENETICS AND METABOLISM

Improved nutritional management of phenylketonuria by using a diet containing glycomacropeptide compared with amino acids

(2009) Sandra C van Calcar et al.   AMERICAN JOURNAL OF CLINICAL NUTRITION

Phenylalanine tolerance can already reliably be assessed at the age of 2 years in patients with PKU

(2009) F. J. van Spronsen et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Adults with late diagnosed PKU and severe challenging behaviour: a randomised placebo-controlled trial of a phenylalanine-restricted diet

(2009) P J Lee et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Reassessment of phenylalanine tolerance in adults with phenylketonuria is needed as body mass changes

(2009) Erin L. MacLeod et al.   MOLECULAR GENETICS AND METABOLISM

Psychiatric symptoms and disorders in phenylketonuria☆

(2009) V.L. Brumm et al.   MOLECULAR GENETICS AND METABOLISM