Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy

Autor: Bernert, G., Knipp, F., Buyse, G.M., Goemans, N., van den Hauwe, M., Voit, T., Doppler, V., Gidaro, T., Cuisset, J.-M., Coopman, S., Schara, U., Lutz, S., Kirschner, J., Borell, S., Will, M., D'Angelo, M.G., Brighina, E., Gandossini, S., Gorni, K., Falcier, E., Politano, L., D'Ambrosio, P., Taglia, A., Verschuuren, J.J.G.M., Straathof, C.S.M., Vílchez Padilla, J.J., Muelas Gómez, N., Sejersen, T., Hovmöller, M., Jeannet, P.-Y., Bloetzer, C., Iannaccone, S., Castro, D., Tennekoon, G., Finkel, R., Bönnemann, C., McDonald, C., Henricson, E., Joyce, N., Apkon, S., Richardson, R.C., McDonald, Craig M., Meier, Thomas, Voit, Thomas, Schara, Ulrike, Straathof, Chiara S.M., D'Angelo, M. Grazia, Bernert, Günther, Cuisset, Jean-Marie, Finkel, Richard S., Goemans, Nathalie, Rummey, Christian, Leinonen, Mika, Spagnolo, Paolo, Buyse, Gunnar M. ^*

Publikováno v: In Neuromuscular Disorders August 2016 26(8):473-480

Treatment effect of idebenone on inspiratory function in patients with Duchenne muscular dystrophy

Autor: Buyse, G.M., Voit, Thomas, Schara, Ulrike, Straathof, C.S.M., D’Angelo, M.G., Bernert, G., Cuisset, J.-M., Finkel, Richard S., Goemans, N., Rummey, Christian, Leinonen, Mika, Mayer, Oscar H., Spagnolo, Paolo, Meier, Thomas, McDonald, Craig M., Knipp, F., Van den Hauwe, M., Doppler, V., Gidaro, T., Coopman, S., Lutz, S., Kirschner, J., Borell, S., Will, M., Brighina, E., Gandossini, S., Gorni, K., Falcier, E., Politano, L., D’Ambrosio, P., Taglia, A., Verschuuren, J.J.G.M., Vílchez Padilla, J.J., Muelas Gómez, N., Sejersen, T., Hovmöller, M., Jeannet, P.-Y., Bloetzer, C., Iannaccone, S., Castro, D., Tennekoon, G., Bönnemann, C., Henricson, E., Joyce, N., Apkon, S., Richardson, R.C.

Publikováno v: Pediatric Pulmonology
Neuromuscular Disorders, 26, S156-S157
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname

Assessment of dynamic inspiratory function may provide valuable information about the degree and progression of pulmonary involvement in patients with Duchenne muscular dystrophy (DMD). The aims of this study were to characterize inspiratory function

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93a0077205a66f9bc9de03ec355058ac
https://hdl.handle.net/1887/112636

An international prospective, longitudinal study of the natural history and functional status of patients with myotubular myopathy

Autor: Annoussamy, M., Landy, H., Ramsdell, D., Nelken, M., Muntoni, F., Bonnemann, C., Bharucha, D., Dowling, J. J., Amburgey, K., Lilien, C., Ollivier, G., Laporte, J., Biancalana, V., Schara, Ulrike, Cuisset, J. M., DAmico, A., Deconinck, N., Jeannet, P. Y., Klein, A., Fluss, J., Mayer, M., Seferian, A. M., Le Moing, A. G., Gidaro, T., Hogrel, J. Y., Mingozzi, F., Buj-Bello, A., Voit, Thomas, Servais, L.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=unidue___bib::3f19df5c3d026ac706a93bac80dab0ee

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