1. Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene. Issue 6 (1st June 1999) Authors: Chapon, F; Latour, P; Diraison, P; Schaeffer, S; Vandenberghe, A Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 66:Issue 6(1999) Page Start: 779 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q. Issue 1 (1st July 1997) Authors: Notelet, L; Chapon, F; Khoury, S; Vahedi, K; Chodkiewicz, J P; Courtheoux, P; Iba-Zizen, M T; Cabanis, E A; Lechevalier, B; Tournier-Lasserve, E; Houtteville, J P Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 63:Issue 1(1997) Page Start: 40 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A. Issue 5 (November 1996) Authors: Chapon, F; Diraison, P; Lechevalier, B; Chazot, G; Viader, F; Bonnebouche, C; Vandenberghe, A; Timmerman, V; Van Broeckhoven, C; Vandenberghe, A Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 61:Issue 5(1996) Page Start: 535 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗