Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)

  1. Pinós, T.
  2. Andreu, A.L.
  3. Bruno, C.
  4. Hadjigeorgiou, G.M.
  5. Haller, R.G.
  6. Laforêt, P.
  7. Lucía, A.
  8. Martín, M.A.
  9. Martinuzzi, A.
  10. Navarro, C.
  11. Oflazer, P.
  12. Pouget, J.
  13. Quinlivan, R.
  14. Sacconi, S.
  15. Scalco, R.S.
  16. Toscano, A.
  17. Vissing, J.
  18. Vorgerd, M.
  19. Wakelin, A.
  20. Martí, R.
  21. Baruch, N.
  22. Ortega, F.J.
  23. San-Millán, B.
  24. Vieitez, I.
  25. Vavla, M.
  26. Musumeci, O.
  27. Scalco, R.
  28. Hadjgeorgiou, G.
  29. Zintzaras, E.
  30. Zülow, E.
  31. Haller, R.
  32. Durmus, H.
  33. Santalla, A.
  34. Show all authors +
Journal:
Orphanet Journal of Rare Diseases

ISSN: 1750-1172

Year of publication: 2020

Volume: 15

Issue: 1

Type: Article

DOI: 10.1186/S13023-020-01455-Z GOOGLE SCHOLAR lock_openOpen access editor

Sustainable development goals

Data source: Scopus