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

Jörg Klepper

University of Essen

Department of Pediatric Neurology

Hufelandstrasse 55

D-45122 Essen

Germany

[email]@uni-essen.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • University of Essen, Department of Pediatric Neurology, Hufelandstrasse 55, D-45122 Essen, Germany. 2001 - 2005
  • Department of Pediatrics and Pediatric Neurology, University of Essen, Germany. 2001 - 2005

References

  1. Bench meets bedside: a 10-year-old girl and amino acid residue glycine 75 of the facilitative glucose transporter GLUT1. Klepper, J., Salas-Burgos, A., Gertsen, E., Fischbarg, J. Biochemistry (2005) [Pubmed]
  2. Seizure control and acceptance of the ketogenic diet in GLUT1 deficiency syndrome: a 2- to 5-year follow-up of 15 children enrolled prospectively. Klepper, J., Scheffer, H., Leiendecker, B., Gertsen, E., Binder, S., Leferink, M., Hertzberg, C., Näke, A., Voit, T., Willemsen, M.A. Neuropediatrics (2005) [Pubmed]
  3. Effects of the ketogenic diet in the glucose transporter 1 deficiency syndrome. Klepper, J., Diefenbach, S., Kohlschütter, A., Voit, T. Prostaglandins Leukot. Essent. Fatty Acids (2004) [Pubmed]
  4. Impaired glucose transport into the brain: the expanding spectrum of glucose transporter type 1 deficiency syndrome. Klepper, J. Curr. Opin. Neurol. (2004) [Pubmed]
  5. Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro. Klepper, J., Flörcken, A., Fischbarg, J., Voit, T. Eur. J. Pediatr. (2003) [Pubmed]
  6. Progressive dystonia in a 12-year-old boy. Klepper, J., Schaper, J., Raca, G., Coryell, J., Das, S., Hayflick, S.J., Voit, T. Eur. J. Paediatr. Neurol. (2003) [Pubmed]
  7. Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain-- a review. Klepper, J., Voit, T. Eur. J. Pediatr. (2002) [Pubmed]
  8. Introduction of a ketogenic diet in young infants. Klepper, J., Leiendecker, B., Bredahl, R., Athanassopoulos, S., Heinen, F., Gertsen, E., Flörcken, A., Metz, A., Voit, T. J. Inherit. Metab. Dis. (2002) [Pubmed]
  9. Autosomal dominant transmission of GLUT1 deficiency. Klepper, J., Willemsen, M., Verrips, A., Guertsen, E., Herrmann, R., Kutzick, C., Flörcken, A., Voit, T. Hum. Mol. Genet. (2001) [Pubmed]
  10. Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene. Klepper, J., Monden, I., Guertsen, E., Voit, T., Willemsen, M., Keller, K. FEBS Lett. (2001) [Pubmed]
 
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