Hypereosinophilic syndrome (HES) represents a heterogeneous group of diseases, some of which are being clarified by recent advances in molecular genetics. It is very rare in children. Uncertainties in classification and lack of prospective studies make therapeutic decisions difficult. The authors report two cases of HES in which steroid therapy was effective.
P., F., P., D., Acquaviva, A., A., T., F., T., D., C., et al. (2009). hypereosinophilic syndrome in childhood: clinical and molecular features in two cases. PEDIATRIC HEMATOLOGY AND ONCOLOGY, 26(3), 129-135.
hypereosinophilic syndrome in childhood: clinical and molecular features in two cases
ACQUAVIVA, ANTONIO;
2009-01-01
Abstract
Hypereosinophilic syndrome (HES) represents a heterogeneous group of diseases, some of which are being clarified by recent advances in molecular genetics. It is very rare in children. Uncertainties in classification and lack of prospective studies make therapeutic decisions difficult. The authors report two cases of HES in which steroid therapy was effective.File | Dimensione | Formato | |
---|---|---|---|
dambro3.pdf
non disponibili
Tipologia:
Post-print
Licenza:
NON PUBBLICO - Accesso privato/ristretto
Dimensione
307.86 kB
Formato
Adobe PDF
|
307.86 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
https://hdl.handle.net/11365/25509
Attenzione
Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo