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. Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlations. Issue 7 (1st May 2014) Authors: Bricout, M; Grévent, D; Lebre, A S; Rio, M; Desguerre, I; De Lonlay, P; Valayannopoulos, V; Brunelle, F; Rötig, A; Munnich, A; Boddaert, N Journal: Journal of medical genetics Issue: Volume 51:Issue 7(2014) Page Start: 429 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. E-047 Vessel wall imaging and brain arteriovenous malformations: initial description of enhancement patterns. (22nd July 2019) Authors: Garzelli, L; Boulouis, G; Blauwblomme, T; Levy, R; Boddaert, N; Ben Hassen, W; Trystram, D; Rodriguez, C; Dangouloff-Ross, V; Nataf, F; Oppenheim, C; Brunelle, F; Edjlali-Goujon, M; Naggara, O Journal: Journal of neurointerventional surgery Issue: Volume 11(2019)Supplement 1 Page Start: A72 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. E-065 Ruptured brain arterio-venous malformations in children and adults: angioarchitectural variations at presentation across the lifespan. (22nd July 2019) Authors: Garzelli, L; Shotar, E; Blauwblomme, T; Sourour, N; Alias, Q; Mathon, B; Kossorotoff, M; Degos, V; Gariel, F; Boddaert, N; Brunelle, F; Meyer, P; Naggara, O; Clarençon, F; Boulouis, G Journal: Journal of neurointerventional surgery Issue: Volume 11(2019)Supplement 1 Page Start: A83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Magnetic resonance imaging for abnormally invasive placenta: the added value of intravenous gadolinium injection. (27th June 2016) Authors: Millischer, A‐E; Salomon, LJ; Porcher, R; Brasseur‐Daudruy, M; Gourdier, A‐L; Hornoy, P; Silvera, S; Loisel, D; Tsatsaris, V; Delorme, B; Boddaert, N; Ville, Y; Sentilhes, L Journal: BJOG Issue: Volume 124:Number 1(2017:Jan.) Page Start: 88 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy. Issue 1 (December 2015) Authors: Perrault, I; Halbritter, J; Porath, J; Gerard, X; Braun, D; Gee, H; Fathy, H; Saunier, S; Cormier-Daire, V; Thomas, S; Attié-Bitach, T; Boddaert, N; Taschner, M; Schueler, M; Lorentzen, E; Lifton, R; Otto, E; Bastin, P; Kaplan, J; Hildebrandt, F Journal: Cilia Issue: Volume 4:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. NSRG-05. SAFETY OF ULTRASOUND-INDUCED BLOOD-BRAIN BARRIER OPENING IN PEDIATRIC PATIENTS WITH REFRACTORY SUS-TENTORIAL MALIGNANT BRAIN TUMORS BEFORE CHEMOTHERAPY ADMINISTRATION – THE SONOKID CLINICAL TRIAL. Issue 2 (22nd June 2018) Authors: Beccaria, K; Canney, M; Bouchoux, G; Zohar, S; Boddaert, N; Bourdeaut, F; Doz, F; Dufour, C; Grill, J; Carpentier, A; Puget, S Journal: Neuro-oncology Issue: Volume 20:Issue 2(2018)supplement 2 Page Start: i146 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking impairment. (4th October 2012) Authors: Thauvin‐Robinet, C; Thomas, S; Sinico, M; Aral, B; Burglen, L; Gigot, N; Dollfus, H; Rossignol, S; Raynaud, M; Philippe, C; Badens, C; Touraine, R; Gomes, C; Franco, B; Lopez, E; Elkhartoufi, N; Faivre, L; Munnich, A; Boddaert, N; Maldergem, L Van Journal: Clinical genetics Issue: Volume 84:Number 1(2013:Jul.) Page Start: 86 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations. Issue 10 (26th August 2008) Authors: Bahi-Buisson, N; Poirier, K; Boddaert, N; Saillour, Y; Castelnau, L; Philip, N; Buyse, G; Villard, L; Joriot, S; Marret, S; Bourgeois, M; Van Esch, H; Lagae, L; Amiel, J; Hertz-Pannier, L; Roubertie, A; Rivier, F; Pinard, J M; Beldjord, C; Chelly, J Journal: Journal of medical genetics Issue: Volume 45:Issue 10(2008) Page Start: 647 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗