Editorial on EJPN focus section on E.U. paediatric MOG consortium consensus statements

por Neuteboom, R.F., Deiva, K., Rostasy, K.
Publicado 2020

ADA2 deficiency: case report of a new phenotype and novel mutation in two sisters

por Uettwiller, F, Sarrabay, G, Rodero, M P, Rice, G I, Lagrue, E, Marot, Y, Deiva, K, Touitou, I, Crow, Y J, Quartier, P
Publicado 2016