Phenylalanine intakes of 1- to 6-year-old children with phenylketonuria undergoing therapy.

No abstract is available for this paper.

• Publication year

  1983

• Venue

  American Journal of Clinical Nutrition

• Publication date

  1983-11-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1093/AJCN/38.5.694PMID 6637861
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Preliminary CommuniCation

  2001cited by this paper
• Excess weight among children with phenylketonuria.

  1982cited by this paper
• The need of essential amino acids in children. An evaluation based on the intake of phenylalanine, tyrosine, leucine, isoleucine, and valine in children with phenylketonuria, tyrosine amino transferase defect, and maple syrup urine disease.

  1980cited by this paper
• The diagnosis of phenylketonuria: a report from the Collaborative Study of Children Treated for Phenylketonuria.

  1980cited by this paper
• Physical growth in phenylketonuria: II. Growth of treated children in the PKU collaborative study from birth to 4 years of age.

  1979cited by this paper
• Methods of dietary inception in infants with PKU.

  1978cited by this paper
• Nutrient intake of treated infants with phenylketonuria.

  1977cited by this paper
• Collaborative study of children treated for phenylketonuria: study design.

  1977cited by this paper
• A computerized procedure for estimating nutrient intake.

  1976cited by this paper
• Calculation of the amino acid requirements of children at different ages by the factorial method.

  1975cited by this paper
• Protein intake of well-nourished children and adolescents.

  1973cited by this paper
• REQUIREMENTS FOR PROTEIN AND ESSENTIAL AMINO ACIDS IN EARLY INFANCY 1 Studies with a Soy‐Isolate Formula

  1973cited by this paper
• Nutritional management in phenylketonuria.

  1971cited by this paper
• Responses of children with phenylketonuria to dietary treatment.

  1971cited by this paper
• Diets of preschool children in the North Central Region. Calories, proteins, fat, and carbohydrate.

  1971cited by this paper
• Malnutrition with Early Treatment of Phenylketonuria

  1970cited by this paper
• Growth and nutrition in treated phenylketonuric patients.

  1970cited by this paper
• The Effect of Immobilization and Sensory Restriction on Children with Phenylketonuria

  1968cited by this paper
• PHENYLALANINE MAINTENANCE IN PHENYLKETONURIA *

  1967cited by this paper
• Composition of foods: raw, processed, prepared.

  1963cited by this paper
• A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.

  1963cited by this paper
• Amino acid requirements of children: minimal needs of threonine, valine and phenylalanine based on nitrogen balance method.

  1962cited by this paper
• The amino acid requirements of infants.

  1961cited by this paper
• Phenylketonuria. I. Dietary management of infants and young children.

  1961cited by this paper
• The diagnosis of phenylketonuria.

  1961cited by this paper
• A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria.

  1958cited by this paper
• Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.

  1955cited by this paper
• The effects of a phenylalanine-free and phenylalanine-poor diet in phenylpyruvic oligophrenis.

  1954cited by this paper
• Nutritional intake of children. I. Calories, carbohydrate, fat and protein.

  1953cited by this paper
• Influence of phenylalanine intake on phenylketonuria.

  1953cited by this paper

• Dietary interventions for phenylketonuria.

  2020cites this paper
• The complete European guidelines on phenylketonuria: diagnosis and treatment

  2017cites this paper
• Is overweight an issue in phenylketonuria?

  2013cites this paper
• Molecular Genetics and Metabolism

  2013cites this paper
• Nutrition in phenylketonuria.

  2011cites this paper
• Dietary interventions for phenylketonuria.

  2010cites this paper
• Recommendations for protein and energy intakes by patients with phenylketonuria

  2009cites this paper
• Summary of findings from the United States Collaborative Study of children treated for phenylketonuria

  2009cites this paper
• Six-year follow up of phenylalanine intakes and plasma phenylalanine concentrations

  2005influential citation
• Nutrient intakes and physical growth of children with phenylketonuria undergoing nutrition therapy.

  2003cites this paper
• Dental disease indices and caries related oral microflora in children with phenylketonuria.

  2001cites this paper
• Dietary interventions for phenylketonuria.

  2000cites this paper
• Growth and skeletal maturation in children with phenylketonuria

  1994cites this paper
• [Phenylketonuria: illness experience and coping mechanisms].

  1993cites this paper
• Iron status and iron supplementation in children with classical phenylketonuria.

  1993cites this paper
• School performance and intellectual outcome in adolescents with phenylketonuria

  1993cites this paper
• Psychological and social findings in adolescents with phenylketonuria

  1992cites this paper
• Formation, nutritional value, and safety of D-amino acids.

  1991cites this paper
• Vitamin B-6 status, energy and protein intakes, and amino acids in the diets and plasma of school-aged patients with Phenylketonuria : implications for an improved nutritional treatment

  1990cites this paper
• Phenylketonuria and Hyperphenylalaninemia

  1987cites this paper
• Bibliography of developmental medicine and child neurology: selected books and articles received in 1984.

  1985cites this paper
• The nutritive value and safety of D-phenylalanine and D-tyrosine in mice.

  1984cites this paper