Claudio Pignata
Department of Pediatrics
"Federico II" University
Naples
Italy
Name/email consistency: high
- Interleukin 12 receptor deficiency in a child with recurrent bronchopneumonia and very high IgE levels. Palamaro, L., Giardino, G., Santamaria, F., Romano, R., Fusco, A., Montella, S., Salerno, M., Ursini, M.V., Pignata, C. Ital. J. Pediatr (2012)
- FOXN1 mutation abrogates prenatal T-cell development in humans. Vigliano, I., Gorrese, M., Fusco, A., Vitiello, L., Amorosi, S., Panico, L., Ursini, M.V., Calcagno, G., Racioppi, L., Del Vecchio, L., Pignata, C. J. Med. Genet. (2011)
- Human clinical phenotype associated with FOXN1 mutations. Pignata, C., Fusco, A., Amorosi, S. Adv. Exp. Med. Biol. (2009)
- A lesson for unraveling complex aspects of novel immunodeficiencies from the human equivalent of the nude/SCID phenotype. Pignata, C. J. Hematother. Stem Cell Res. (2002)
- Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation. Pignata, C., Gaetaniello, L., Masci, A.M., Frank, J., Christiano, A., Matrecano, E., Racioppi, L. Blood (2001)
- Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children. Pignata, C., Alessio, M., Ramenghi, U., Bonissoni, S., Difranco, D., Brusco, A., Matrecano, E., Franzese, A., Dianzani, I., Dianzani, U. Clin. Exp. Immunol. (2000)
