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Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)

Autor: Scalco, R. S., Lucia, A., Santalla, A., Martinuzzi, A., Vavla, M., Reni, G., Toscano, A., Musumeci, O., Voermans, N. C., Kouwenberg, C. V., Laforet, P., San-Millan, B., Vieitez, I., Siciliano, G., Kuhnle, E., Trost, R., Sacconi, S., Stemmerik, M. G., Durmus, H., Kierdaszuk, B., Wakelin, A., Andreu, A. L., Pinos, T., Marti, R., Quinlivan, R., Vissing, J., Baruch, N., Ortega, F. J., Martin, M. A., Navarro, C., Millan, B. S., Castelli, M., Zucchi, F., Bruno, C., Scalco, R., Hadjgeorgiou, G., Zintzaras, E., Vorgerd, M., Zulow, E., Haller, R., Oflazer, P., Pouget, J.

Publikováno v: Orphanet Journal of Rare Diseases, 15
Orphanet Journal of Rare Diseases, 15, 1
Orphanet Journal of Rare Diseases
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
ABACUS. Repositorio de Producción Científica
Universidad Europea (UEM)
Scalco, R S, Lucia, A, Santalla, A, Martinuzzi, A, Vavla, M, Reni, G, Toscano, A, Musumeci, O, Voermans, N C, Kouwenberg, C V, Laforêt, P, San-Millán, B, Vieitez, I, Siciliano, G, Kühnle, E, Trost, R, Sacconi, S, Stemmerik, M G, Durmus, H, Kierdaszuk, B, Wakelin, A, Andreu, A L, Pinós, T, Marti, R, Quinlivan, R, Vissing, J & EUROMAC Consortium 2020, ' Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC) ', Orphanet Journal of Rare Diseases, vol. 15, no. 1, pp. 330 . https://doi.org/10.1186/s13023-020-01562-x

Background The European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC) was launched to register rare muscle glycogenoses in Europe, to facilitate recruitment for research trials and to learn about the phenotypes an

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