Screening for Metabolic Disorders: How Are We Doing?
- 1 October 1993
- journal article
- review article
- Published by Elsevier in Pediatric Clinics of North America
- Vol. 40 (5) , 1073-1085
- https://doi.org/10.1016/s0031-3955(16)38624-2
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Current issues in neonatal screening for cystic fibrosis and implications of the CF gene discoveryPediatric Pulmonology, 1991
- IVth international conference on newborn screening for cystic fibrosis: Concluding remarksPediatric Pulmonology, 1991
- Regulation of galactose metabolism: Implications for therapyJournal of Inherited Metabolic Disease, 1990
- Late onset of distinct neurologic syndromes in galactosemic siblingsNeurology, 1989
- Congenital Adrenal HyperplasiaNew England Journal of Medicine, 1987
- Folinic acid therapy in treatment of dihydropteridine reductase deficiencyThe Journal of Pediatrics, 1987
- Paired comparisons between early treated PKU children and their matched sibling controls on intelligence and school achievement test results at eight years of ageJournal of Inherited Metabolic Disease, 1983
- Speech and language deficits in early-treated children with galactosemiaPublished by Elsevier ,1983
- Maternal Phenylketonuria and HyperphenylalaninemiaNew England Journal of Medicine, 1980
- PHENYLPYRUVIC OLIGOPHRENIAArchives of Neurology & Psychiatry, 1937