Literature DB >> 14005688

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

A N WEINBERG.   

Abstract

Entities:  

Keywords:  GALACTOSE/blood

Mesh：

Substances：

Year:  1961        PMID： 14005688

Source DB:  PubMed          Journal:  Metabolism        ISSN： 0026-0495            Impact factor:   8.694


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  8 in total

Review 1.  [ON THE ROLE OF BLOOD CELLS IN THE DIAGNOSIS OF HEREDITARY METABOLIC DISEASES].

Authors:  F LINNEWEH
Journal:  Klin Wochenschr       Date:  1963-10-01

2.  [Enzymatic methods for the diagnosis of galactosemia and galactose deficiency].

Authors:  H Kruas; E Mönch
Journal:  Klin Wochenschr       Date:  1970-04-01

3.  Detection of heterozygotes for galactokinase deficiency in a human population.

Authors:  J S Mayes; R Guthrie
Journal:  Biochem Genet       Date:  1968-11       Impact factor: 1.890

4.  [Galactokinase defect in a newborn infant].

Authors:  F Linneweh; E Schaumlöffel; M Vetrella
Journal:  Klin Wochenschr       Date:  1970-01-01

5.  UDP-glucose: alpha-D-galactose-1-phosphate uridylytransferase activity in cultured human fibroblasts.

Authors:  J D Russell; R DeMars
Journal:  Biochem Genet       Date:  1967-06       Impact factor: 1.890

6.  [Debré-De Toni-Fanconi syndrome with glycogenosis of the liver].

Authors:  B Bauer
Journal:  Klin Wochenschr       Date:  1968-03-15

7.  THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES. A PRESUMED TEST FOR HETEROZYGOUS CARRIERS OF THE GALACTOSEMIC DEFECT.

Authors:  A ROBINSON
Journal:  J Exp Med       Date:  1963-09-01       Impact factor: 14.307

8.  Galactose metabolism in transferase-deficient galactosaemic and normal long-term lymphoid cell lines.

Authors:  N G Beratis; L Wilbur
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982
  8 in total

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