Diagnosis features of pediatric Gaucher disease patients in the era of enzymatic therapy, a national-base study from the Spanish Registry of Gaucher Disease

  1. Andrade-Campos, M.
  2. Alfonso, P.
  3. Irun, P.
  4. Armstrong, J.
  5. Calvo, C.
  6. Dalmau, J.
  7. Domingo, M.-R.
  8. Barbera, J.-L.
  9. Cano, H.
  10. Fernandez-Galán, M.-A.
  11. Franco, R.
  12. Gracia, I.
  13. Gracia-Antequera, M.
  14. Ibañez, A.
  15. Lendinez, F.
  16. Madruga, M.
  17. Martin-Hernández, E.
  18. O'Callaghan, M.D.M.
  19. Del Soto, A.P.
  20. Del Prado, Y.R.
  21. Sancho-Val, I.
  22. Sanjurjo, P.
  23. Pocovi, M.
  24. Giraldo, P.
Journal:
Orphanet Journal of Rare Diseases

ISSN: 1750-1172

Year of publication: 2017

Volume: 12

Issue: 1

Type: Article

DOI: 10.1186/S13023-017-0627-Z GOOGLE SCHOLAR lock_openOpen access editor

Sustainable development goals

Data source: Scopus