Three novel mutations reflect the variety of defects causing phenotypically diverse X-linked hyper-IgM syndrome

Por LÓPEZ-GRANADOS, E, CAMBRONERO, R, FERREIRA, A, FONTÁN, G, GARCÍA-RODRÍGUEZ, M C
Publicado em 2003

Naturally occurring Bruton's tyrosine kinase mutations have no dominant negative effect in an X-linked agammaglobulinaemia cellular model

Por Pérez de Diego, R, López-Granados, E, Rivera, J, Ferreira, A, Fontán, G, Bravo, J, García Rodríguez, MC, Bolland, S
Publicado em 2008

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders

Por Packwood, K, Drewe, E, Staples, E, Webster, D, Witte, T, Litzman, J, Egner, W, Sargur, R, Sewell, W, Lopez-Granados, E, Seneviratne, S L, Powell, R J, Ferry, B L, Chapel, H M
Publicado em 2010

A mutation in X-linked inhibitor of apoptosis (G466X) leads to memory inflation of Epstein–Barr virus-specific T cells

Por Lopez-Granados, E, Stacey, M, Kienzler, A-K, Sierro, S, Willberg, C B, Fox, C P, Rigaud, S, Long, H M, Hislop, A D, Rickinson, A B, Patel, S, Latour, S, Klenerman, P, Chapel, H
Publicado no Clin Exp Immunol (2014)