Cargando…
Identification of type I interferonopathies using blood interferon signature: the experience of a pediatric rheumatology center
Autores principales: | Volpi, S, Santori, E, Picco, P, Rice, G, Caorsi, R, Martini, A, Crow, Y, Candotti, F, Gattorno, M |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600053/ http://dx.doi.org/10.1186/1546-0096-13-S1-P142 |
Ejemplares similares
-
Type I interferonopathies in pediatric rheumatology
por: Volpi, Stefano, et al.
Publicado: (2016) -
Enlarging the clinical spectrum of SAVI syndrome
por: Caorsi, R, et al.
Publicado: (2015) -
Monogenic interferonopathy presenting as CMV infection in infancy
por: Schütz, C, et al.
Publicado: (2015) -
Mosaic tetrasomy 9p: a mendelian interferonopathy associated with pediatric-onset overlap myositis
por: Frémond, M-L, et al.
Publicado: (2015) -
Type I interferon–mediated monogenic autoinflammation: The type I interferonopathies, a conceptual overview
por: Rodero, Mathieu P., et al.
Publicado: (2016)