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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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

[email]@jefferson.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • 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. 2004 - 2005
  • Department of Pediatrics, University of Pennsylvania School of Medicine, The Children's Hospital of Philadelphia, Philadelphia, USA. 2003 - 2004
  • Children's Research Institute, Children's National Medical Center, Department of Pediatrics, George Washington University School of Medicine and Health Sciences, USA. 2004

References

  1. 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) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
  4. Extended [13C]galactose oxidation studies in patients with galactosemia. Berry, G.T., Reynolds, R.A., Yager, C.T., Segal, S. Mol. Genet. Metab. (2004) [Pubmed]
  5. 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) [Pubmed]
 
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