1. A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency. Issue 1 (23rd October 2010) Authors: Lebre, A S; Rio, M; Faivre d'Arcier, L; Vernerey, D; Landrieu, P; Slama, A; Jardel, C; Laforêt, P; Rodriguez, D; Dorison, N; Galanaud, D; Chabrol, B; Paquis-Flucklinger, V; Grévent, D; Edvardson, S; Steffann, J; Funalot, B; Villeneuve, N; Valayannopoulos, V; de Lonlay, P Journal: Journal of medical genetics Issue: Volume 48:Issue 1(2011) Page Start: 16 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome. Issue 1 (16th January 2004) Authors: Bénit, P; Slama, A; Cartault, F; Giurgea, I; Chretien, D; Lebon, S; Marsac, C; Munnich, A; Rötig, A; Rustin, P Journal: Journal of medical genetics Issue: Volume 41:Issue 1(2004) Page Start: 14 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Two year maintenance treatment of duodenal ulcer disease with ranitidine 150 mg: a prospective multicentre randomised study. GEMUD (Groupe d'Etude de la Maladie Ulcéreuse Duodénale). Issue 12 (December 1993) Authors: Ruszniewski, P; Slama, A; Pappo, M; Mignon, M Journal: Gut Issue: Volume 34:Issue 12(1993) Page Start: 1662 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗