Studies on the origin of faecal amino acids in cystic fibrosis
Open Access
- 1 July 1970
- Vol. 11 (7) , 600-609
- https://doi.org/10.1136/gut.11.7.600
Abstract
Evidence is presented which demonstrates that excess faecal amino acids in cystic fibrosis are derived from unabsorbed dietary protein. Changes in the absorption of fat and nitrogen have little effect on the amino-acid patterns.Keywords
This publication has 25 references indexed in Scilit:
- Use of medium-chain triglyceride diets in children with malabsorption.Archives of Disease in Childhood, 1969
- Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease.Archives of Disease in Childhood, 1967
- TYROSINE METABOLISM AND FqCAL AMINOACIDS IN CYSTIC FIBROSIS OF THE PANCREASThe Lancet, 1967
- L-tryptophan metabolism in phenylketonuriaThe Journal of Pediatrics, 1966
- Excretion of 1-aminocyclopentanecarboxylic acid in man and the ratBiochimica et Biophysica Acta, 1962
- The intestinal absorption defect in cystinuriaGut, 1961
- Über den Bau der apolaren Bereiche der Kollagenfaser; Abbau mit Kollagenase. Aminosäuresequenzen des Kollagens, IIIHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1961
- The Effect of Pancreatin Therapy on Fat Absorption and Nitrogen Retention in Children with Fibrocystic Disease of the PancreasArchives of Disease in Childhood, 1955
- FÆCAL EXCRETION OF AMINO-ACIDS IN INFANTSThe Lancet, 1951
- DETERMINATION OF THE PLASMA GLYCINE AFTER GELATIN FEEDING AS A DIAGNOSTIC PROCEDURE FOR PANCREATIC FIBROSISJournal of Clinical Investigation, 1949