Black children deficient in galactose 1-phosphate uridyltransferase: Correlation of activity and immunoreactive protein in erythrocytes and leukocytes-Reference-Cited by-同舟云学术

Black children deficient in galactose 1-phosphate uridyltransferase: Correlation of activity and immunoreactive protein in erythrocytes and leukocytes

Published:1997-06 Issue:6 Volume:130 Page:972-980
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Landt Michael,Ritter Detlef,Lai Kent,Benke Paul J.,Elsas Louis J.,Steiner Robert D.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference38 articles.

1. Disorders of galactose metabolism;Segal,1995

2. Long-term prognosis in galactosemia: results of a survey of 350 cases;Waggoner;J Inherit Metab Dis,1990

3. Developmental aspects of galactosemia from infancy to childhood;Fishler;Clin Pediatr,1980

4. Newborn screening;US Public Health Service;Am Fam Physician,1994

5. Galactosemia: screening and diagnosis;Beutler;Clin Biochem,1991

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1. Alterations of galactose metabolism caused by deficit of galactose-1-phosphate uridylyltransferase activity: An overview of galactosemia type I;Molecular Nutrition: Carbohydrates;2019

2. GALK inhibitors for classic galactosemia;Future Medicinal Chemistry;2014-06

3. Impaired NADPH oxidase activity in peripheral blood lymphocytes of galactosemia patients;Experimental Biology and Medicine;2013-07

4. Cryptic residual GALT activity is a potential modifier of scholastic outcome in school age children with classic galactosemia;Journal of Inherited Metabolic Disease;2013-01-15

5. Galactosemia: When is it a newborn screening emergency?;Molecular Genetics and Metabolism;2012-05