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

Timothy M. Cox

Department of Medicine

University of Cambridge

Addenbrooke's Hospital

UK

[email]@medschl.cam.ac.uk

Name/email consistency: low

 
 
 
 
 
 
 

Affiliation

  • Department of Medicine, University of Cambridge, Addenbrooke's Hospital, UK. 2001 - 2006

References

  1. Damage at the cellular and organ levels in LSDs: possibility for prevention/reversibility with ERT. Cox, T.M., Beck, M. Acta. Paediatr. Suppl (2006) [Pubmed]
  2. Biomarkers in lysosomal storage diseases: a review. Cox, T.M. Acta. Paediatr. Suppl (2005) [Pubmed]
  3. Substrate reduction therapy for lysosomal storage diseases. Cox, T.M. Acta. Paediatr. Suppl (2005) [Pubmed]
  4. The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statement. Cox, T.M., Aerts, J.M., Andria, G., Beck, M., Belmatoug, N., Bembi, B., Chertkoff, R., Vom Dahl, S., Elstein, D., Erikson, A., Giralt, M., Heitner, R., Hollak, C., Hrebicek, M., Lewis, S., Mehta, A., Pastores, G.M., Rolfs, A., Miranda, M.C., Zimran, A. J. Inherit. Metab. Dis. (2003) [Pubmed]
  5. The genetic consequences of our sweet tooth. Cox, T.M. Nat. Rev. Genet. (2002) [Pubmed]
  6. Hemochromatosis--neonatal and young subjects. Cox, T.M., Halsall, D.J. Blood Cells Mol. Dis. (2002) [Pubmed]
  7. Gaucher disease: understanding the molecular pathogenesis of sphingolipidoses. Cox, T.M. J. Inherit. Metab. Dis. (2001) [Pubmed]
 
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