Lakaye, Bernard ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biochimie et physiologie humaine et pathologique
de Nijs, Laurence ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biochimie et physiologie humaine et pathologique
Leon, Christine
Grisar, Thierry ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biochimie et physiologie humaine et pathologique
Delgado-Escueta A.V. Advances in genetics of juvenile myoclonic epilepsies. Epilepsy Currents 2007, 7:61-67.
de Nijs L., Lakaye B., Coumans B., et al. EFHC1, a protein mutated in juvenile myoclonic epilepsy, associates with the mitotic spindle through its N-terminus. Experimental Cell Research 2006, 312:2872-2879.
Grisar T., de Nijs L., Chanas G., et al. Some genetic and biochemical aspects of myoclonus. Neurophysiologie Clinique 2006, 36:271-279.
Guerrini R., Marini C. Genetic malformations of cortical development. Experimental Brain Research 2006, 173(2):322-333.
Guerrini R., Fillipi T. Neuronal migration disorders, genetics and epileptogenesis. Journal of Child Neurology 2005, 20(4):287-299.
Ikeda K., Brown J.A., Yagi T., et al. Rib 72, a conserved protein associated with the ribbon compartment of flagellar A-microtubules and potentially involved in the linkage between outer doublet microtubules. Journal of Biological Chemistry 2003, 278:7725-7734.
King S.M. Axonemal protofilaments ribbons, DM10 domains, and the link to juvenile myoclonic epilepsy. Cell Motility and the Cytoskeleton 2006, 63:245-253.
Meencke H.J., Janz D. Neuropathological findings in primary generalized epilepsy: A study of eight cases. Epilepsia 1984, 25(1):8-21.
Suzuki T., Delgado-Escueta A.V., Aguan K., et al. Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nature Genetics 2004, 36(8):842-849.