Clinical and Biochemical Observations in Galactosemia
Author:
Open Access
- 1 September 1957
- journal article
- research article
- Published by Elsevier in The American Journal of Clinical Nutrition
- Vol. 5 (5) , 527-532
Abstract
KURT J. ISSELBACHER, M.D.; Clinical and Biochemical Observations in Galactosemia, The American Journal of Clinical Nutrition, Volume 5, Issue 5, 1 September 19Keywords
This publication has 19 references indexed in Scilit:
- Biochemical Mutations in Man and MicroorganismsScience, 1957
- Studies on Metabolism of Carbon-14-Labeled Galactose in a Galactosemic IndividualScience, 1957
- DIPHOSPHOPYRIDINE NUCLEOTIDE, A COFACTOR FOR GALACTO-WALDENASE1Journal of the American Chemical Society, 1956
- Galactosemia, a congenital defect in a nucleotide transferaseBiochimica et Biophysica Acta, 1956
- A Study of the Genetics of GalactosaemiaArchives of Disease in Childhood, 1955
- The Amino-aciduria in GalactosaemiaArchives of Disease in Childhood, 1955
- Human Nutrition and the Sophistication of Foods and Feeding HabitsBMJ, 1955
- Galactose 1-phosphate in galactose cataractBiochimica et Biophysica Acta, 1955
- Uridyl Transferases and the Formation of Uridine Triphosphate : Uridyl Transferases and the Formation of Uridine DiphosphogalactoseNature, 1953
- Amino-aciduria in GalactosaemiaBMJ, 1952