1. Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotype. (1st December 2022) Authors: Coste, T.; Aloui, C.; Petit, F.; Moutton, S.; Devisme, L.; Wells, C. F.; Leboucq, N.; Verpillat, P.; Yvert, M.; Rivier, F.; Tournier‐Lasserve, E. Journal: Ultrasound in obstetrics & gynecology Issue: Volume 60:Number 6(2022) Page Start: 805 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Infantile systemic hyalinosis. (June 2017) Authors: Meyer, P.; Tournier, C.; Bessis, D.; Rolland, A.; Carme, E.; Roubertie, A.; Ribrault, A.; Hajj-Verkindere, E.; Lebre, A.S.; Rivier, F. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e199 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Pediatric cerebral venous thrombosis: Description and prognosis according to the physiopathological mechanism in a population of 40 cases. (June 2017) Authors: Durand, S.; Meyer, P.; Leboucq, N.; Langlois, C.; Carneiro, M.; Roubertie, A.; Walther-Louvier, U.; Cuntz, D.; Leydet, J.; Plan, O.; Combes, C.; Cambonie, G.; Rivier, F. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e174 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗