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Auteur Hébert L |
Documents disponibles écrits par cet auteur (4)
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Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Hébert L ; Puymirat J ; Saulnier J ; Vial C ; Remec JF | AFM-TELETHON | 2011Introduction. Myotonic dystrophy type 1 (DM1) is a multisystem disorder that demonstrates variable symptoms and rates of progression. Muscle weakness is considered one of the main problems with a clinical picture that is characterized by distal [...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Hébert L ; Puymirat J ; Saulnier J | AFM-TELETHON | 2011Introduction. In Myotonic Dystrophy type 1 (DM1), few consensuses have emerged with regard to muscle strength impairments, and level of function. Distal weakness first appears and is usually identified after 9 to 10 years' duration of the illnes[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Côte C ; Bassem H ; Hébert L ; Janier M ; Puymirat J | 2008The aim of the study was to evaluate if a typical pattern of muscular involvement could be identified, and if correlation exists between severity of MRI anomalies and clinical findings. MRI findings were edema and fatty degeneration, ranging fro[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Hiba B ; Richard N ; Hébert L ; Vial C ; Saulnier J ; Nejjari M ; Remec JF ; Côte C ; Bouhour F ; Puymirat J ; Janier M | 2008An objective assessment of disease progression and muscle damage is required to prove therapies for muscle degeneration. In this context, we propose an objective MRI-based method for the assessment of the Tibias Anterior (TA) muscle degeneration[...]