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

P. De Jonghe

Flanders Interuniversity Institute for Biotechnology

Born-Bunge Foundation

University of Antwerp

Division of Neurology



Name/email consistency: high



  • Flanders Interuniversity Institute for Biotechnology, Born-Bunge Foundation, University of Antwerp, Division of Neurology, Belgium. 2001
  • Department of Biochemistry, Flanders Interuniversity Institute for Biotechnology (VIB), University of Antwerp (UIA), University Hospital Antwerpen (UZA), Belgium. 1999
  • Department of Biochemistry, University Hospital Antwerp, Belgium. 1999


  1. Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E. De Jonghe, P., Mersivanova, I., Nelis, E., Del Favero, J., Martin, J.J., Van Broeckhoven, C., Evgrafov, O., Timmerman, V. Ann. Neurol. (2001) [Pubmed]
  2. The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype. De Jonghe, P., Timmerman, V., Ceuterick, C., Nelis, E., De Vriendt, E., Löfgren, A., Vercruyssen, A., Verellen, C., Van Maldergem, L., Martin, J.J., Van Broeckhoven, C. Brain (1999) [Pubmed]
  3. A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype. De Jonghe, P., Timmerman, V., Nelis, E., De Vriendt, E., Löfgren, A., Ceuterick, C., Martin, J.J., Van Broeckhoven, C. Arch. Neurol. (1999) [Pubmed]
  4. Molecular diagnostic testing in Charcot-Marie-Tooth disease and related disorders. Approaches and results. De Jonghe, P., Nelis, E., Timmerman, V., Löfgren, A., Martin, J.J., Van Broeckhoven, C. Ann. N. Y. Acad. Sci. (1999) [Pubmed]
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