A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency.

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; Desguerre, I; Brunelle, F; Bonnefont, J P; Rötig, A; Munnich, A; Boddaert, N

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; Desguerre, I; Brunelle, F; Bonnefont, J P; Rötig, A; Munnich, A; Boddaert, N.

Affiliation

Lebre AS; Université Paris Descartes, AP-HP Hôpital Necker-Enfants Malades et Inserm U781 et U797, Départements de Génétique, de Radiologie pédiatrique et des Maladies du développement, Paris, France. anne-sophie.lebre@nck.aphp.fr

J Med Genet ; 48(1): 16-23, 2011 Jan.

Article in En | MEDLINE | ID: mdl-20972245

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain / Magnetic Resonance Imaging / Mitochondrial Diseases / Electron Transport Complex I Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: J Med Genet Year: 2011 Document type: Article Affiliation country: Country of publication:

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