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L.P. van den Heuvel

Nijmegen Centre for Mitochondrial Disorders

Department of Pediatrics

University Medical Centre Nijmegen

Geert Grooteplein 10

Netherlands

[email]@*.umcn.nl

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Affiliations

Nijmegen Centre for Mitochondrial Disorders, Department of Pediatrics, University Medical Centre Nijmegen, Geert Grooteplein 10, Netherlands. 2004
University Medical Center Nijmegen, Laboratory for Pediatrics and Neurology, Department of Pediatrics, Geert Grooteplein 20, Netherlands. 2003
Department of Pediatrics, University Medical Centre Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, Netherlands. 2002

References

Biochemical examination of fibroblasts in the diagnosis and research of oxidative phosphorylation (OXPHOS) defects. van den Heuvel, L.P., Smeitink, J.A., Rodenburg, R.J. Mitochondrion (2004) [Pubmed]
Proteomics and neuromuscular diseases: theoretical concept and first results. van den Heuvel, L.P., Farhoud, M.H., Wevers, R.A., van Engelen, B.G., Smeitink, J.A. Ann. Clin. Biochem. (2003) [Pubmed]
Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2). van den Heuvel, L.P., Assink, K., Willemsen, M., Monnens, L. Hum. Genet. (2002) [Pubmed]