Newborn screening for galactosemia and other galactose metabolic defects
- 1 June 1978
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 92 (6), 871-877
- https://doi.org/10.1016/s0022-3476(78)80351-5
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
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- Prenatal diagnosis of galactosemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- Galactose?1?phosphate uridyl transferase in fibroblasts: Isozymes in normal and variant statesAnnals of Human Genetics, 1975
- Rennes-like variant of galactosemia: Clinical and biochemical studiesThe Journal of Pediatrics, 1975
- Unstable galactose-1-phosphate uridyl transferase: A new variant of galactosemiaThe Journal of Pediatrics, 1971
- An improved electrophoretic procedure for galactose-l-phosphate uridyl transferase: Demonstration of multiple activity bands with the duarte variantBiochemical and Biophysical Research Communications, 1969
- Electrophoretic abnormality of galactose-1-phosphate uridyl transferase in galactosemiaBiochemical and Biophysical Research Communications, 1969
- An improved procedure for the assay of hemolysate galactose-1-phosphate uridyl transferase activity by the use of 14C-labeled galactose-1-phosphateClinica Chimica Acta; International Journal of Clinical Chemistry, 1967
- Galactosemia: Symptomatic and asymptomatic homozygotes in one Negro sibshipThe Journal of Pediatrics, 1966
- Improved method for measuring galactose-1-phosphate uridyl transferase activity of erythrocytesClinica Chimica Acta; International Journal of Clinical Chemistry, 1966