Accumulation of galactose-1-phosphate in the galactosemic fetus despite maternal milk avoidance
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference12 articles.
1. Hypergonadotropic hypogonadism in female patients with galactosemia;Kaufman;N Engl J Med,1981
2. Speech and language deficits in early treated children with galactosemia;Waisbren;J Pediatr,1983
3. Curious neurologic sequelae in galactosemia;Lo;Pediatrics,1984
4. Galactosemia: Thirty years on. The experience of a generation;Komrower;J Inher Metab Dis,1982
5. Prenatal diagnosis of galactosemia;Ng;Clin Chim Acta,1977
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1. The hypergonadotropic hypogonadism conundrum of classic galactosemia;Human Reproduction Update;2022-12-13
2. Disorders of galactose metabolism;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020
3. Galactose 1‐phosphate accumulates to high levels in galactose‐treated cells due to low GALT activity and absence of product inhibition of GALK;Journal of Inherited Metabolic Disease;2019-12-17
4. Disorders of Galactose Metabolism;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2015
5. Disorders of Galactose Metabolism;Inborn Metabolic Diseases;2012
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