Gerard T. Berry
Department of Pediatrics
Division of Human Genetics and Molecular Biology and the Metabolic Research Laboratory
University of Pennsylvania School of Medicine
The Children's Hospital of Philadelphia
USA
Name/email consistency: high
- Elements of diabetic nephropathy in a patient with GLUT 2 deficiency. Berry, G.T., Baynes, J.W., Wells-Knecht, K.J., Szwergold, B.S., Santer, R. Mol. Genet. Metab. (2005)
- The rate of de novo galactose synthesis in patients with galactose-1-phosphate uridyltransferase deficiency. Berry, G.T., Moate, P.J., Reynolds, R.A., Yager, C.T., Ning, C., Boston, R.C., Segal, S. Mol. Genet. Metab. (2004)
- Phosphoinositide deficiency due to inositol depletion is not a mechanism of lithium action in brain. Berry, G.T., Buccafusca, R., Greer, J.J., Eccleston, E. Mol. Genet. Metab. (2004)
- Extended [13C]galactose oxidation studies in patients with galactosemia. Berry, G.T., Reynolds, R.A., Yager, C.T., Segal, S. Mol. Genet. Metab. (2004)
- Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apnea. Berry, G.T., Wu, S., Buccafusca, R., Ren, J., Gonzales, L.W., Ballard, P.L., Golden, J.A., Stevens, M.J., Greer, J.J. J. Biol. Chem. (2003)