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

Editor

Personal info

Please enable Javascript support in your browser to use this application.

Instructions on how to enable JavaScript on different browsers can be found here: http://www.google.com/support/bin/answer.py?answer=23852.

Flanders Interuniversity Institute for Biotechnology

Born-Bunge Foundation

University of Antwerp

Division of Neurology

Belgium

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

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]
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]
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]
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]