Literature DB >> 5522111

[Galactokinase defect in a newborn infant].

F Linneweh, E Schaumlöffel, M Vetrella.   

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Year:  1970        PMID： 5522111     DOI： 10.1007/bf01486125

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN： 0023-2173


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  2 in total

1.  Detection of congenital galactosemia and the carrier state using galactose C14 and blood cells.

Authors:  A N WEINBERG
Journal:  Metabolism       Date:  1961-09       Impact factor: 8.694

2.  Hypergalactosemia and galactosuria due to galactokinase deficiency in a newborn.

Authors:  O Thalhammer; R Gitzelmann; M Pantlitschko
Journal:  Pediatrics       Date:  1968-09       Impact factor: 7.124
  2 in total
  2 in total

1.  Hereditary galactokinase deficiency.

Authors:  J G Cook; N A Don; T P Mann
Journal:  Arch Dis Child       Date:  1971-08       Impact factor: 3.791

Review 2.  Clinical features of galactokinase deficiency: a review of the literature.

Authors:  A M Bosch; H D Bakker; A H van Gennip; J V van Kempen; R J A Wanders; F A Wijburg
Journal:  J Inherit Metab Dis       Date:  2002-12       Impact factor: 4.982
  2 in total

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