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Wolkoff Nathalie

Main Referenced Co-authors
de Nijs, Laurence  (2)
Grisar, Thierry  (2)
Lakaye, Bernard  (2)
Coumans, Bernard  (1)
Delgado-Escueta, Antonio (1)
Main Referenced Keywords
axogenesis (1); axonogenèse (1); dendritogenesis (1); dendritogenèse (1); Epilepsie (1);
Main Referenced Unit & Research Centers
GIGA-Neuroscience (1)
Main Referenced Disciplines
Neurology (2)
Neurosciences & behavior (1)

Publications (total 3)

The most downloaded
131 downloads
de Nijs, L., Wolkoff, N., Coumans, B., Delgado-Escueta, A., Grisar, T., & Lakaye, B. (2012). Mutations of EFHC1, linked to juvenile myoclonic epilepsy, disrupt radial and tangential migrations during brain development. Human Molecular Genetics, 21 (23), 5106-17. doi:10.1093/hmg/dds356 https://hdl.handle.net/2268/135479

The most cited

28 citations (OpenCitations)

de Nijs, L., Wolkoff, N., Coumans, B., Delgado-Escueta, A., Grisar, T., & Lakaye, B. (2012). Mutations of EFHC1, linked to juvenile myoclonic epilepsy, disrupt radial and tangential migrations during brain development. Human Molecular Genetics, 21 (23), 5106-17. doi:10.1093/hmg/dds356 https://hdl.handle.net/2268/135479

Wolkoff, N. (2014). Influence des formes mutées d'EFHC1 (ou myoclonine 1), une protéine impliquée dans l'épilepsie myoclonique juvénile, sur la corticogenèse cérébrale [Doctoral thesis, Université de Liège]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/315314

de Nijs, L., Wolkoff, N., Grisar, T., & Lakaye, B. (2013). Juvenile myoclonic epilepsy as a possible neurodevelopmental disease: role of EFHC1 or Myoclonin 1. Epilepsy and Behavior, 28, 58-S60.
Peer Reviewed verified by ORBi

de Nijs, L., Wolkoff, N., Coumans, B., Delgado-Escueta, A., Grisar, T., & Lakaye, B. (2012). Mutations of EFHC1, linked to juvenile myoclonic epilepsy, disrupt radial and tangential migrations during brain development. Human Molecular Genetics, 21 (23), 5106-17. doi:10.1093/hmg/dds356
Peer Reviewed verified by ORBi

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