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

Peter Schadewaldt

Deutsches Diabetes Zentrum

Abteilung Klinische Biochemie und Pathobiochemie

Auf'm Hennekamp 65

D-40225 Düsseldorf



Name/email consistency: high



  • Deutsches Diabetes Zentrum, Abteilung Klinische Biochemie und Pathobiochemie, Auf'm Hennekamp 65, D-40225 Düsseldorf, Germany. 2010
  • German Diabetic Centre, Department of Clinical Biochemistry and Pathobiochemistry, UKD, University of Düsseldorf, Düsseldorf, Germany. 2009
  • Klinik für Allgemeine Pädiatrie, Universitätsklinikum Düsseldorf, Düsseldorf, Germany. 2003 - 2004
  • Diabetes Forschungsinstitut, Klinische Biochemie Auf'm Hennekamp 65, Düsseldorf, Germany. 1997 - 2001


  1. Longitudinal assessment of intellectual achievement in patients with classical galactosemia. Schadewaldt, P., Hoffmann, B., Hammen, H.W., Kamp, G., Schweitzer-Krantz, S., Wendel, U. Pediatrics (2010) [Pubmed]
  2. Biochemical monitoring of pregnancy and breast feeding in five patients with classical galactosaemia--and review of the literature. Schadewaldt, P., Hammen, H.W., Kamalanathan, L., Wendel, U., Schwarz, M., Bosch, A.M., Guion, N., Janssen, M., Boers, G.H. Eur. J. Pediatr. (2009) [Pubmed]
  3. Age dependence of endogenous galactose formation in Q188R homozygous galactosemic patients. Schadewaldt, P., Kamalanathan, L., Hammen, H.W., Wendel, U. Mol. Genet. Metab. (2004) [Pubmed]
  4. Galactonate determination in urine by stable isotope dilution gas chromatography-mass spectrometry. Schadewaldt, P., Hammen, H.W., Stolpmann, S., Kamalanathan, L., Wendel, U. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. (2004) [Pubmed]
  5. Renal excretion of galactose and galactitol in patients with classical galactosaemia, obligate heterozygous parents and healthy subjects. Schadewaldt, P., Killius, S., Kamalanathan, L., Hammen, H.W., Strassburger, K., Wendel, U. J. Inherit. Metab. Dis. (2003) [Pubmed]
  6. Stable-isotope dilution analysis of galactose metabolites in human erythrocytes. Schadewaldt, P., Kamalanathan, L., Hammen, H.W., Wendel, U. Rapid Commun. Mass Spectrom. (2003) [Pubmed]
  7. Whole-body L-leucine oxidation in patients with variant form of maple syrup urine disease. Schadewaldt, P., Bodner-Leidecker, A., Hammen, H.W., Wendel, U. Pediatr. Res. (2001) [Pubmed]
  8. Analysis of concentration and (13)C enrichment of D-galactose in human plasma. Schadewaldt, P., Hammen, H.W., Loganathan, K., Bodner-Leidecker, A., Wendel, U. Clin. Chem. (2000) [Pubmed]
  9. Renal clearance of branched-chain L-amino and 2-oxo acids in maple syrup urine disease. Schadewaldt, P., Hammen, H.W., Ott, A.C., Wendel, U. J. Inherit. Metab. Dis. (1999) [Pubmed]
  10. Significance of L-alloisoleucine in plasma for diagnosis of maple syrup urine disease. Schadewaldt, P., Bodner-Leidecker, A., Hammen, H.W., Wendel, U. Clin. Chem. (1999) [Pubmed]
  11. Application of isotope-selective nondispersive infrared spectrometry (IRIS) for evaluation of [13C]octanoic acid gastric-emptying breath tests: comparison with isotope ratio-mass spectrometry (IRMS). Schadewaldt, P., Schommartz, B., Wienrich, G., Brösicke, H., Piolot, R., Ziegler, D. Clin. Chem. (1997) [Pubmed]
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