Cognitive functioning, neurologic status and brain imaging in classical galactosemia Francine Ratner KaufmanCammie McBride-ChangMarvin D. Nelson OriginalPaper Pages: S2 - S5
In vivo study of brain metabolism in galactosemia by1H and31P magnetic resonance spectroscopy Harald E. MöllerKurt UllrichHans-Georg Koch OriginalPaper Pages: S8 - S13
Gonadal function in galactosemics and in galactose-intoxicated animals James B. Gibson OriginalPaper Pages: S14 - S20
A molecular approach to galactosemia Louis J. Elsas IISharon LangleyPhilip P. Dembure OriginalPaper Pages: S21 - S27
Regulation of galactose-1-phosphate uridyltransferase gene expression R. A. Heidenreich OriginalPaper Pages: S28 - S32
Partial deficiency of galactose-1-phosphate uridyltransferase R. TitzelmannN. U. Bosshard OriginalPaper Pages: S40 - S44
Galactose-1-phosphate in the pathophysiology of galactosemia R. Gitzelmann OriginalPaper Pages: S45 - S49
The role of polyols in the pathophysiology of hypergalactosemia Gerard T. Berry OriginalPaper Pages: S53 - S64
Defective galactosylation in galactosemia: Is low cell UDPgalactose an explanation? Stanton Segal OriginalPaper Pages: S65 - S71
Measurements of uridine diphosphate glucose and uridine diphosphate galactose — an appraisal Henry N. Kirkman OriginalPaper Pages: S72 - S74
Nucleotide sugars: Determination of cellular levels and discrepancies in results Y. S. Shin BriefCommunication Pages: S75 - S76
Hidden sources of galactose in the environment Phyllis B. AcostaKenneth C. Gross OriginalPaper Pages: S87 - S92
Leguminosae in the diet: The raffinose-stachyose question Ulrich N. WiesmannBarbara Rosé-BeutlerRoger Schlüchter OriginalPaper Pages: S93 - S96
Questions and worries: The voice of the Galactosemia Support Groups Sue Bevington BriefCommunication Pages: S103 - S105
