TY  - JOUR 
AU  - Karazi, W.
AU  - Scalco, R.S.
AU  - Stemmerik, M.G.
AU  - Løkken, N.
AU  - Lucia, A.
AU  - Santalla, A.
AU  - Martinuzzi, A.
AU  - Vavla, M.
AU  - Reni, G.
AU  - Toscano, A.
AU  - Musumeci, O.
AU  - Kouwenberg, C.V.
AU  - Laforêt, P.
AU  - San Millan Tejado, Beatriz
AU  - Vieitez González, Irene
AU  - Siciliano, G.
AU  - Kühnle, E.
AU  - Trost, R.
AU  - Sacconi, S.
AU  - Durmus, H.
AU  - Kierdaszuk, B.
AU  - Wakelin, A.
AU  - Andreu, A.L.
AU  - Pinós, T.
AU  - Marti, R.
AU  - Quinlivan, R.
AU  - Vissing, J.
AU  - Voermans, N.C.
PY  - 2023
SN  - 1750-1172
UR  - http://hdl.handle.net/20.500.11940/21305
AB  - Background: The European registry for individuals with GSD5 and other muscle glycogenosis (EUROMAC) was launched to register rare muscle glycogenosis in Europe, to facilitate recruitment for research trials and to learn about the phenotypes and...
LA  - eng
KW  - Humans
KW  - Glycogen Storage Disease Type V
KW  - Quality of Life
KW  - Social Participation
KW  - Functional Status
KW  - Glycogen Storage Disease
KW  - Fatigue
TI  - Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation
DO  - 10.1186/s13023-023-02825-z
T2  - Orphanet Journal of Rare Diseases
KW  - AS Vigo
KW  - CHUVI
VL  - 18
ER  -