SAETTINI FRANCESCO

Ruolo: 
Assegnista di ricerca
Settore scientifico disciplinare: 
PEDIATRIA GENERALE E SPECIALISTICA (MED/38)

Pubblicazioni

  • Saettini, F., Castelli, I., Provenzi, M., Fazio, G., Quadri, M., Cazzaniga, G., et al. (2020). A novel homozygous disruptive PRF1 variant (K285Sfs*4) causes very early-onset of familial hemophagocytic lymphohystiocytosis type 2. PEDIATRIC HEMATOLOGY AND ONCOLOGY, 1-5. Dettaglio
  • Saettini, F., Herriot, R., Prada, E., Nizon, M., Zama, D., Marzollo, A., et al. (2020). Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients. JOURNAL OF CLINICAL IMMUNOLOGY, 40(6), 851-860. Dettaglio
  • Saettini, F., Fazio, G., Corti, P., Quadri, M., Bugarin, C., Gaipa, G., et al. (2020). Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations. CLINICAL IMMUNOLOGY, 218. Dettaglio
  • Saettini, F., Cattoni, A., Redaelli, M., Silvestri, D., Ferrari, G., Biondi, A., et al. (2020). Primary immunodeficiencies, autoimmune hyperthyroidism, coeliac disease and systemic lupus erythematosus in childhood immune thrombocytopenia. ACTA PAEDIATRICA. Dettaglio
  • Saettini, F., Cattoni, A., D'Angiò, M., Corti, P., Maitz, S., Pagni, F., et al. (2020). Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond-like syndrome. BRITISH JOURNAL OF HAEMATOLOGY, 189(4), e171-e174. Dettaglio