The first aim of this study is the determination of the endogenous galactose, galactitol and galactonate pool sizes in the galactosemic patient, all of these being factors in the body galactose burden.
The second aim i s the determination of the in vivo galactose oxidation rate in the galactosemic patient.
The third aim i s the determination whether GALT activity can be modulated in vivo by pharmocologic administration of uridine, folate or progesterone.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000240-35S1
Application #
6219804
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
35
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Children's Hospital of Philadelphia
Department
Type
DUNS #
073757627
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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