International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up

  1. Altassan, R.
  2. Péanne, R.
  3. Jaeken, J.
  4. Barone, R.
  5. Bidet, M.
  6. Borgel, D.
  7. Brasil, S.
  8. Cassiman, D.
  9. Cechova, A.
  10. Coman, D.
  11. Corral, J.
  12. Correia, J.
  13. de la Morena-Barrio, M.E.
  14. de Lonlay, P.
  15. Dos Reis, V.
  16. Ferreira, C.R.
  17. Fiumara, A.
  18. Francisco, R.
  19. Freeze, H.
  20. Funke, S.
  21. Gardeitchik, T.
  22. Gert, M.
  23. Girad, M.
  24. Giros, M.
  25. Grünewald, S.
  26. Hernández-Caselles, T.
  27. Honzik, T.
  28. Hutter, M.
  29. Krasnewich, D.
  30. Lam, C.
  31. Lee, J.
  32. Lefeber, D.
  33. Marques-da-Silva, D.
  34. Martinez, A.F.
  35. Moravej, H.
  36. Õunap, K.
  37. Pascoal, C.
  38. Pascreau, T.
  39. Patterson, M.
  40. Quelhas, D.
  41. Raymond, K.
  42. Sarkhail, P.
  43. Schiff, M.
  44. Seroczyńska, M.
  45. Serrano, M.
  46. Seta, N.
  47. Sykut-Cegielska, J.
  48. Thiel, C.
  49. Tort, F.
  50. Vals, M.-A.
  51. Videira, P.
  52. Witters, P.
  53. Zeevaert, R.
  54. Morava, E.
  55. Show all authors +
Journal:
Journal of Inherited Metabolic Disease

ISSN: 1573-2665 0141-8955

Year of publication: 2019

Volume: 42

Issue: 1

Pages: 5-28

Type: Review

DOI: 10.1002/JIMD.12024 GOOGLE SCHOLAR lock_openOpen access editor