TY  - GEN 
AU  - Pinós, T.
AU  - Andreu, A. L.
AU  - Bruno, C.
AU  - Hadjigeorgiou, G. M.
AU  - Haller, R. G.
AU  - Laforêt, P.
AU  - Lucía, A.
AU  - Martín, M. A.
AU  - Martinuzzi, A.
AU  - Navarro Fernández-Balbuena, Carmen
AU  - Oflazer, P.
AU  - Pouget, J.
AU  - Quinlivan, R.
AU  - Sacconi, S.
AU  - Scalco, R. S.
AU  - Toscano, A.
AU  - Vissing, J.
AU  - Vorgerd, M.
AU  - Wakelin, A.
AU  - Martí, R.
PY  - 2020
SN  - 1750-1172
UR  - http://hdl.handle.net/20.500.11940/16759
AB  - BACKGROUND: International patient registries are of particular importance for rare disorders, as they may contribute to overcome the lack of knowledge derived from low number of patients and limited awareness of these diseases, and help to learn more...
KW  - Muscles
KW  - Humans
KW  - Registries
KW  - Quality of Life
KW  - Rare Diseases
TI  - Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)
DO  - 10.1186/s13023-020-01455-z
KW  - IISGS
VL  - 15
ER  -