Gain of RNA function in pathological cases: Focus on myotonic dystrophy von Klein, A.F., Gasnier, E., Furling, D.

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Homogeneity of peraluminous SiO2–B2O3–Al2O3–Na2O–CaO–Nd2O3 glasses: Effect of neodymium content von Gasnier, E., Bardez-Giboire, I., Montouillout, V., Pellerin, N., Allix, M., Massoni, N., Ory, S., Cabie, M., Poissonnet, S., Massiot, D.

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Assessment of lower limbs in FSHD: The ActiMyo as a new outcome for home-monitoring von Gidaro, T, Gasnier, E, Denis, S, Lilien, C, Grelet, M, Rigaud, A, Moraux, A, Dorveaux, E, Vissiere, D, Servais, L

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Movement monitoring at home and during study visits identifies sources of variability in 6MWT performance in Duchenne muscular dystrophy von Servais, L, Grelet, M, Seferian, A, Gasnier, E, Gargaun, E, Straub, V, Mercuri, E, Voit, T, Laforet, G, Dorveau, E, Vissiere, D, Muntoni, F

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New criteria for assessing the achievement of upper limbs in FSHD patients von Gasnier, E, Gidaro, T, Grelet, M, Denis, S, Rigaud, A, Lilien, C, Seferian, A, Moraux, A, Dorveaux, E, Vissière, D, Servais, L

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Longitudinal results of magneto-inertial motion analysis in Duchenne muscular dystrophy ambulant patients von Seferian, A, Gargaun, E, Grelet, M, Gasnier, E, Lilien, C, Gillabert, S, Duchene, D, Voit, T, Domingos, J. Piscos, Guglieri, M, Straub, V, Leone, D, Mercuri, E, Laforet, G, Muntoni, F, Dorveaux, E, Vissiere, D, Servais, L

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Feasibility of magneto-inertial motion analysis in non-ambulant patients with spinal muscular atrophy von Seferian, A, Quicke, G, Gidaro, T, Gargaun, E, Gasnier, E, Pereon, Y, Daron, A, Cances, C, Vuillerot, C, Goemans, N, Laugel, V, Cuisset, J, Schara, U, Marquet, A, Chabanon, A, Annoussamy, M, Vissiere, D, Servais, L

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VP.27 Potential of the Keeogo+, a lightweight wearable powered assistive exoskeleton in patients with neuromuscular disorders: preliminary findings von Feigean, R., Afroun, C., Gasnier, E., Benveniste, O., Bassez, G., Hogrel, J., Bachasson, D.

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VP.26 Potential of the MyoSuit, a lightweight wearable lower-limb cable-actuated exoskeleton in patients with neuromuscular disorders: preliminary findings von Feigean, R., Afroun, C., Gasnier, E., Benveniste, O., Hogrel, J., Bassez, G., Bachasson, D.

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15P Prospective, longitudinal study of the natural history of paediatric patients in France with LAMA2 related dystrophies von Seferian, A., Gasnier, E., Peretti, M., Duchene, D., Lagrue, E., Vuillerot, C., Walther-Louvier, U., García-de-la-Banda, M. Gómez, Grange, A., Carlier, R., Reyngoudt, H., Marty, B., Colella, M., Quijano-Roy, S.

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P.191Maximal stride velocity detects positive and negative changes over 6- month-time period in ambulant patients with Duchenne muscular dystrophy von Servais, L., Gidaro, T., Seferian, A., Gasnier, E., Daron, A., Ulinici, A., Grelet, M., Vissiere, D.

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D.P.4.08 P16 triggers premature senescence of congenital DM1 myoblasts von Butler-Browne, G.S, Bigot, A, Gasnier, E, Mouly, V, Furling, D

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DUCHENNE MUSCULAR DYSTROPHY - PHYSIOTHERAPY: P.301Home based movement monitoring allows pivotal trials in DMD with ten times less patients than classical outcomes measures von Servais, L., Gasnier, E., Grelet, M., Gidaro, T., Seferian, A., Vissieres, D.

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DUCHENNE MUSCULAR DYSTROPHY - PHYSIOTHERAPY von Lilien, C., Grelet, M., Gasnier, E., Gidaro, T., Seferian, A., Rigaud, A., Vissière, D., Servais, L.

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DUCHENNE MUSCULAR DYSTROPHY - PHYSIOTHERAPY von Servais, L., Gasnier, E., Grelet, M., Gidaro, T., Seferian, A., Vissieres, D.

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DUCHENNE MUSCULAR DYSTROPHY - PHYSIOTHERAPY: P.312Factors influencing spontaneous maximal stride speed in individual Duchenne muscular dystrophy boys von Lilien, C., Grelet, M., Gasnier, E., Gidaro, T., Seferian, A., Rigaud, A., Vissière, D., Servais, L.

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OUTCOME MEASURES von Servais, L., Gidaro, T., Seferian, A., Gasnier, E., Daron, A., Ulinici, A., Annoussamy, M., Grelet, M., Vissiere, D.

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OUTCOME MEASURES: P.189Measuring fatigability during real-life assessment in spinal muscular atrophy von Servais, L., Gidaro, T., Seferian, A., Gasnier, E., Daron, A., Ulinici, A., Annoussamy, M., Grelet, M., Vissiere, D.

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Activities of daily living detection using home activity monitoring device in Duchenne muscular dystrophy patients von Moraux, A., Beaufils, B., Grelet, M., Seferian, A., Gasnier, E., Gidaro, T., Dorveaux, E., Vissiere, D., Servais, L.

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P.458 - Activities of daily living detection using home activity monitoring device in Duchenne muscular dystrophy patients von Moraux, A., Beaufils, B., Grelet, M., Seferian, A., Gasnier, E., Gidaro, T., Dorveaux, E., Vissiere, D., Servais, L.

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