Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease.
Open Access
- 1 December 1967
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 42 (226), 682-688
- https://doi.org/10.1136/adc.42.226.682
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Hartnup DiseaseNew England Journal of Medicine, 1965
- AminoaciduriaNew England Journal of Medicine, 1965
- Disorders of Amino-Acid TransportBMJ, 1964
- BIOCHEMICAL ASPECTS OF HARTNUP DISEASE .3. GENERAL DISCUSSION + CONCLUSIONS1964
- The intestinal absorption defect in cystinuriaGut, 1961
- An inborn defect in the metabolism of tyrosine in infants on a normal dietBiochemical Journal, 1960
- Detection of heterozygotes for phenylketonuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1960
- THE METABOLIC DISORDER IN HARTNUP DISEASEQJM: An International Journal of Medicine, 1960
- Renal clearances of amino acids in normal adults and in patients with aminoaciduriaBiochemical Journal, 1960
- HEREDITARY PELLAGRA-LIKE SKIN RASH WITH TEMPORARY CEREBELLAR ATAXIA, CONSTANT RENAL AMINO-ACIDURIA, AND OTHER BIZARRE BIOCHEMICAL FEATURESThe Lancet, 1956