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The American Journal of Clinical Nutrition|February 1, 1980
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 diseaseE Kindt, S Halvorsen
The American Journal of Clinical Nutrition|February 1, 1994
Reduced nutritional status in an elderly population (> 70 y) is probable before disease and possibly contributes to the development of diseaseM Mowé, T Bøhmer, E Kindt
The Orthopedic Clinics of North America|November 24, 2012
Fracture-dislocations of the carpus: perilunate injuryPrasad J Sawardeker, Katie E Kindt, Mark E Baratz
The American Journal of Clinical Nutrition|May 1, 1983
Protein requirements in infants and children: a longitudinal study of children treated for phenylketonuriaE Kindt, K Motzfeldt, S Halvorsen, et al.
The British Journal of Nutrition|May 1, 1984
Is phenylalanine requirement in infants and children related to protein intake?E Kindt, K Motzfeldt, S Halvorsen, et al.
The British Journal of Nutrition|September 1, 1985
Net protein utilization determined by rat bioassay of a protein hydrolysate and a diet for children with phenylketonuriaE Kindt, H Holm, S Halvorsen, et al.
Analytical Biochemistry|August 10, 2000
Quantitative method for biomarkers of collagen degradation using liquid chromatography tandem mass spectrometryE Kindt, D T Rossi, K Gueneva-Boucheva, et al.
Acta Paediatrica Scandinavica|January 1, 1988
Fasting plasma amino acid concentrations in PKU children on two different levels of protein intakeE Kindt, H A Lunde, L R Gjessing, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|November 30, 1989
[Children with phenylketonuria (Fölling's disease). Intellectual functions and psychological adaptation]J Aarseth, I H Vandvik, S Heyerdahl, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 22, 2001
The effect of troglitazone biliary excretion on metabolite distribution and cholestasis in transporter-deficient ratsV E Kostrubsky, M Vore, E Kindt, et al.
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