Availability, accessibility and delivery to patients of the 28 orphan medicines approved by the European Medicine Agency for hereditary metabolic diseases in the MetabERN network
- Heard, J.-M.
- Vrinten, C.
- Schlander, M.
- Bellettato, C.M.
- Van Lingen, C.
- Scarpa, M.
- Matthijs, G.
- Nassogne, M.-C.
- Debray, F.-G.
- Roland, D.
- Chamova, T.
- Kozich, V.
- Pavel, J.
- Zenker, M.
- Lampe, C.
- Das, A.M.
- Hennermann, J.
- Kölker, S.
- Weinhold, N.
- Mohnike, K.
- Gruenert, S.
- Lund, A.M.
- Morales-Conejo, M.
- Del Toro-Riera, M.
- Aldámiz-Echevarría, L.
- Garcia-Silva, M.-T.
- Schiff, M.
- Gouya, L.
- De Lonlay, P.
- Belmatoug, N.
- Germain, D.P.
- Cano, A.
- Dobbelaere, D.
- Jones, S.
- Dawson, C.
- Deegan, P.
- Santra, S.
- Vijay, S.
- Petkovic Ramadza, D.
- Barić, I.
- Žigman, T.
- Pflieger, G.
- Szakszon, K.
- Kaposta, R.
- Gasperini, S.
- Burlina, A.
- Parenti, G.
- Strisciuglio, P.
- Ceccarini, G.
- Federico, A.
- Simonati, A.
- Tumiene, B.
- Huidekoper, H.
- Van Spronsen, F.
- Bosch, A.
- Rubio-Gozalbo, M.-E.
- Visser, G.
- Tangeraas, T.
- Aarsand, A.
- Kieć-Wilk, B.
- Mendes Gaspar, A.-M.S.
- Quelhas, D.
- Leao-Teles, E.
- Azevedo, O.
- Rodriges Silva, E.-M.F.
- De Abreu Freire, L.-M.D.M.
- Martins, E.
- Lajic, S.
- Darin, N.
- Groselj, U.
- Tansek, M.-Z.
- Show all authors +
Journal:
Orphanet Journal of Rare Diseases
ISSN: 1750-1172
Year of publication: 2020
Volume: 15
Issue: 1
Type: Article