1. Early-onset epileptic encephalopathies with "suppression-burst" EEG pattern: Genetic characterization of a European cohort of 70 patients. (June 2017) Authors: Riccardi, F.; Cacciagli, P.; Lacoste, C.; Mignon Ravix, C.; Nagara, M.; Villard, L.; Milh, M. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e167 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. In utero seizures revealing dentato‐olivary dysplasia caused by SCN2A mutation. (9th June 2017) Authors: Sauvestre, F.; Moutton, S.; Badens, C.; Broussin, B.; Carles, D.; Houcinat, N.; Lacoste, C.; Marguet, F.; Pecheux, C.; Villard, L.; Pelluard, F.; Laquerrière, A.; André, G. Journal: Neuropathology & applied neurobiology Issue: Volume 43:Number 7(2017) Page Start: 631 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Is there a justification for hysterectomy in patients with borderline ovarian tumors?. (March 2016) Authors: Ouldamer, L.; Lacoste, C.; Cormier, B.; Arbion, F.; Marret, H.; Jallais, L.; Fignon, A.; Body, G. Journal: Surgical oncology Issue: Volume 25:Number 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome. (1st December 2013) Authors: Lacoste, C.; Leheup, B.; Agouti, I.; Mowat, D.; Giuliano, F.; Badens, C. Journal: Clinical genetics Issue: Volume 86:Number 5(2014:Nov.) Page Start: 502 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗