Profil

Léon Christine

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Main Referenced Co-authors
de Nijs, Laurence  (4)
Grisar, Thierry  (4)
Lakaye, Bernard  (4)
Delgado-Escueta, A. V. (3)
Chanas, G. (2)
Main Referenced Keywords
centrosome (1); EFHC1 (1); Epilepsie myoclonique juvenile (1); epilepsy (1); genetic defects (1);
Main Referenced Disciplines
Neurosciences & behavior (4)
Neurology (1)
Oncology (1)
Anatomy (cytology, histology, embryology...) & physiology (1)

Publications (total 5)

The most downloaded
387 downloads
Leon, C., de Nijs, L., Chanas, G., Delgado-Escueta, A. V., Grisar, T., & Lakaye, B. (2010). Distribution of EFHC1 or myoclonin 1 in mouse neural structures. Epilepsy Research, 88, 196-207. doi:10.1016/j.eplepsyres.2009.11.009 https://hdl.handle.net/2268/75757

The most cited

66 citations (Scopus®)

de Nijs, L., Leon, C., Nguyen, L., LoTurco, J. J., Delgado-Escueta, A. V., Grisar, T., & Lakaye, B. (2009). EFHC1 interacts with microtubules to regulate cell division and cortical development. Nature Neuroscience, 12 (10), 1266-74. doi:10.1038/nn.2390 https://hdl.handle.net/2268/27634

Léon, C. (2010). Exploration des propriétés d’une protéine dont le gène est muté dans certaines familles atteintes d’épilepsie myoclonique juvénile (EMJ) : EFHC1 ou myoclonine 1 [Doctoral thesis, Université de Liège]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/315092

Leon, C., de Nijs, L., Chanas, G., Delgado-Escueta, A. V., Grisar, T., & Lakaye, B. (2010). Distribution of EFHC1 or myoclonin 1 in mouse neural structures. Epilepsy Research, 88, 196-207. doi:10.1016/j.eplepsyres.2009.11.009
Peer Reviewed verified by ORBi

de Nijs, L., Leon, C., Nguyen, L., LoTurco, J. J., Delgado-Escueta, A. V., Grisar, T., & Lakaye, B. (2009). EFHC1 interacts with microtubules to regulate cell division and cortical development. Nature Neuroscience, 12 (10), 1266-74. doi:10.1038/nn.2390
Peer Reviewed verified by ORBi

de Nijs, L., Lakaye, B., Coumans, B., Leon, C., Ikeda, T., Delgado-Escueta, A. V., Grisar, T., & Chanas, G. (10 September 2006). EFHC1, a protein mutated in juvenile myoclonic epilepsy, associates with the mitotic spindle through its N-terminus. Experimental Cell Research, 312 (15), 2872-2879. doi:10.1016/j.yexcr.2006.05.011
Peer Reviewed verified by ORBi

Grisar, T., de Nijs, L., Chanas, G., Leon, C., Coumans, B., Foidart, A., & Lakaye, B. (2006). Some genetic and biochemical aspects of myoclonus. Neurophysiologie Clinique, 36 (5-6, Sep-Dec), 271-279. doi:10.1016/j.neucli.2006.11.002
Peer Reviewed verified by ORBi

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