Patient reported outcomes for phosphomannomutase 2 congenital disorder of glycosylation (PMM2-CDG): listening to what matters for the patients and health professionals.

Autor: Pascoal, C.1,2,3,4 (AUTHOR), Ferreira, I.2 (AUTHOR), Teixeira, C.2,5 (AUTHOR), Almeida, E.2,3 (AUTHOR), Slade, A.6 (AUTHOR), Brasil, S.1,2,3,4 (AUTHOR), Francisco, R.1,2,3,4 (AUTHOR), Ligezka, A. N.7 (AUTHOR), Morava, E.7 (AUTHOR), Plotkin, H.8 (AUTHOR), Jaeken, J.2,9 (AUTHOR), Videira, P. A.1,2,3,4 (AUTHOR), Barros, L.2,10 (AUTHOR), dos Reis Ferreira, V.1,2,3,4 (AUTHOR) sindromecdg@gmail.com
Zdroj: Orphanet Journal of Rare Diseases. 10/29/2022, Vol. 17 Issue 1, p1-22. 22p.
Databáze: Academic Search Ultimate
Nepřihlášeným uživatelům se plný text nezobrazuje