Premsa 22 Setembre, 2016

Participació de la UPIIP a l'ESID 2016

Avui, al congrès de la ESID 2016, diferents membres de la UPIIP i del Servei d'Immunologia de l'Hospital Universitari de la Vall d'Hebron han presentat un total d'11 posters. A continuació, els títols de cada un d'ells.

  1. Newborn screening for Severe Combined Immunodeficiency in Catalonia. Dr. Pere Soler Palacin 
  2. Residual NADPH oxidase activity and Chronic Granulomatous Disease. It is a useful prognostic tool? Dra. Andrea Martín
  3. Oral use of intravenous human immunoglobulin as an adjunctive treatment for recurrent diarrhea in immunocompromised pediatric patients. Jacques G Rivière
  4. The Catalan cohort of patients with primary immunodeficiencies receiving immunoglobulin therapy. The GammaCat Project. Núria Murtra
  5. Functional and molecular characterization of a novel nonsense mutation in IL2RG gene in a family with atypical presentation. Marina Garcia
  6. Extended immunophenotype in patients with activated PI3kδ syndrome (APDS-2) caused by mutations in the PIK3R1 gene. Marina Garcia
  7. The study of Primary Immunodeficiencies: Reference values in children. Marina Garcia
  8. High prevalence of complement C5 p.A252T mutation in African populations: A worldwide study. Clara Franco
  9. Complete Factor I Deficiency. A not so rare immune defect? Clara Franco
  10. Clinical application of next generation sequencing in the genetic diagnosis of primary immunodeficiencies. Roger Colobran
  11. Hemophagocytic syndrome: the challenge of mono-allelic variants. Laura Viñas

Un gran treball en equip!

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