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

Stefan Kölker

Department of General Pediatrics

Division of Inherited Metabolic Diseases

University Hospital Heidelberg

Heidelberg

Germany. Electronic address:

[email]@med.uni-heidelberg.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Hospital Heidelberg, Heidelberg, Germany. Electronic address:. 2005 - 2012

References

  1. Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I - A decade of experience. Kölker, S., Boy, S.P., Heringer, J., Müller, E., Maier, E.M., Ensenauer, R., Mühlhausen, C., Schlune, A., Greenberg, C.R., Koeller, D.M., Hoffmann, G.F., Haege, G., Burgard, P. Mol. Genet. Metab. (2012) [Pubmed]
  2. Diagnosis and management of glutaric aciduria type I - revised recommendations. Kölker, S., Christensen, E., Leonard, J.V., Greenberg, C.R., Boneh, A., Burlina, A.B., Burlina, A.P., Dixon, M., Duran, M., García Cazorla, A., Goodman, S.I., Koeller, D.M., Kyllerman, M., Mühlhausen, C., Müller, E., Okun, J.G., Wilcken, B., Hoffmann, G.F., Burgard, P. J. Inherit. Metab. Dis. (2011) [Pubmed]
  3. Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism. Kölker, S., Sauer, S.W., Hoffmann, G.F., Müller, I., Morath, M.A., Okun, J.G. J. Inherit. Metab. Dis. (2008) [Pubmed]
  4. Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany. Kölker, S., Garbade, S.F., Boy, N., Maier, E.M., Meissner, T., Mühlhausen, C., Hennermann, J.B., Lücke, T., Häberle, J., Baumkötter, J., Haller, W., Muller, E., Zschocke, J., Burgard, P., Hoffmann, G.F. Pediatr. Res. (2007) [Pubmed]
  5. Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I). Kölker, S., Christensen, E., Leonard, J.V., Greenberg, C.R., Burlina, A.B., Burlina, A.P., Dixon, M., Duran, M., Goodman, S.I., Koeller, D.M., Müller, E., Naughten, E.R., Neumaier-Probst, E., Okun, J.G., Kyllerman, M., Surtees, R.A., Wilcken, B., Hoffmann, G.F., Burgard, P. J. Inherit. Metab. Dis. (2007) [Pubmed]
  6. Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency. Kölker, S., Garbade, S.F., Greenberg, C.R., Leonard, J.V., Saudubray, J.M., Ribes, A., Kalkanoglu, H.S., Lund, A.M., Merinero, B., Wajner, M., Troncoso, M., Williams, M., Walter, J.H., Campistol, J., Martí-Herrero, M., Caswill, M., Burlina, A.B., Lagler, F., Maier, E.M., Schwahn, B., Tokatli, A., Dursun, A., Coskun, T., Chalmers, R.A., Koeller, D.M., Zschocke, J., Christensen, E., Burgard, P., Hoffmann, G.F. Pediatr. Res. (2006) [Pubmed]
  7. Methylmalonic acid--an endogenous toxin?. Kölker, S., Okun, J.G. Cell. Mol. Life Sci. (2005) [Pubmed]
 
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