Participación de la UPIIP en la ESID 2016
Hoy, en el congreso de la ESID 2016, diferentes miembros de la UPIIP y del Servicio de Inmunología del Hospital Universitario de la Vall d'Hebron han presentado un total de 11 posters. A continuación, los títulos de cada uno de ellos:
- Newborn screening for Severe Combined Immunodeficiency in Catalonia. Dr. Pere Soler Palacin
- Residual NADPH oxidase activity and Chronic Granulomatous Disease. It is a useful prognostic tool? Dra. Andrea Martín
- Oral use of intravenous human immunoglobulin as an adjunctive treatment for recurrent diarrhea in immunocompromised pediatric patients. Jacques G Rivière
- The Catalan cohort of patients with primary immunodeficiencies receiving immunoglobulin therapy. The GammaCat Project. Núria Murtra
- Functional and molecular characterization of a novel nonsense mutation in IL2RG gene in a family with atypical presentation. Marina Garcia
- Extended immunophenotype in patients with activated PI3kδ syndrome (APDS-2) caused by mutations in the PIK3R1 gene. Marina Garcia
- The study of Primary Immunodeficiencies: Reference values in children. Marina Garcia
- High prevalence of complement C5 p.A252T mutation in African populations: A worldwide study. Clara Franco
- Complete Factor I Deficiency. A not so rare immune defect? Clara Franco
- Clinical application of next generation sequencing in the genetic diagnosis of primary immunodeficiencies. Roger Colobran
- Hemophagocytic syndrome: the challenge of mono-allelic variants. Laura Viñas
¡Un gran trabajo en equipo!
