DELBINI, PAOLA
DELBINI, PAOLA
Dipartimento di Scienze Cliniche e di Comunità
2'-O-methoxyethyl splice-switching oligos correct splicing from IVS2-745 β-thalassemia patient cells restoring HbA production and chain rebalance
2021 A. Dong, V. Ghiaccio, I. Motta, S. Guo, R. Peralta, S.M. Freier, A. Watt, S. Damle, Y. Ikawa, D. Jarocha, M. Chappell, C. Stephanou, P. Delbini, C. Chen, S. Christou, M. Kleanthous, K. Smith-Whitley, D. Manwani, C. Casu, O. Abdulmalik, M.D. Cappellini, S. Rivella, L. Breda
A giant adrenal myelolipoma in a beta-thalassemia major patient : Does ineffective erythropoiesis play a role?
2016 I. Motta, L. Boiocchi, P. Delbini, M. Migone De Amicis, E. Cassinerio, D. Dondossola, G. Rossi, M.D. Cappellini
Activin receptor-ligand trap for the treatment of β-thalassemia : a serendipitous discovery
2020 V. Brancaleoni, I. Nava, P. Delbini, L. Duca, I. Motta
Gene symbol : G6PD. Disease : Glucose-6-phosphate dehydrogenase deficiency
2008 P. Delbini, L. Duca, I. Nava, D. Tavazzi, M.D. Cappellini
Gene symbol : HAMP. Disease : Haemochromatosis, juvenile
2008 P. Delbini, L. Duca, I. Nava, A. Meo, M.D. Cappellini
Genetic variability of TMPRSS6 and its association with iron deficiency anaemia
2010 P. Delbini, V. Vaja, G. Graziadei, L. Duca, I. Nava, C. Refaldi, M.D. Cappellini
Genetic variability of TMPRSS6 gene and its association with iron deficiency anemia
2010 P. Delbini, V. Vaja, G. Graziadei, C. Cesaretti, I. Motta, M.D. Cappellini
Hepcidin mutation in a beta-thalassemia major patient with persistent severe iron overload despite chelation therapy
2010 L. Duca, P. Delbini, I. Nava, M. D. Cappellini, A. Meo
Mutation analysis of hepcidin and ferroportin genes : possible relationship with iron overload in italian prospective blood-donors
2008 L. Duca, P. Delbini, I. Nava, V. Vaja, G. Fiorelli, M.D. Cappellini
Mutation analysis of hepcidin and ferroportin genes in Italian prospective blood donors with iron overload
2009 L. Duca, P. Delbini, I. Nava, V. Vaja, G. Fiorelli, M.D. Cappellini
New epidemiology of Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Italy
2011 G. Graziadei, I. Nava, P. Delbini, D. Tavazzi, L. Duca, M.D. Cappellini
Polymorphisms in TMPRSS6 gene are risk factors for iron deficiency and iron deficiency anemia
2012 A. Marcon, G. Graziadei, P. Delbini, E. Poggiali, M. Soldarini, I. Nava, M.D. Cappellini
Reversal of cardiac complications by deferiprone and deferoxamine combination therapy in a patient affected by a severe type of juvenile hemochromatosis (JH)
2007 G. Fabio, F. Minonzio, P. Delbini, A. Bianchi, M.D. Cappellini
Reversal of hearth failure by deferoxamine and deferiprone combined therapy in a patient affected by severe type juvenile hemochromatosis
2005 G. Fabio, F. Minonzio, P. Delbini, A. Bianchi, M.D. Cappellini
Studio della pro-epcidina sierica e dello stato del ferro nella talassemia major ed intermedia
2007 P. Delbini
Terapia combinata con deferxamina e deferiprone nel trattamento delle complicanze cardiache in un paziente affetto da grave emocromatosi giovanile
2005 G. Fabio, F. Minonzio, P. Delbini, M.D. Cappellini
The autophagy-activating kinase ULK1 mediates clearance of free α-globin in β-thalassemia
2019 C. Lechauve, J. Keith, E. Khandros, S. Fowler, K. Mayberry, A. Freiwan, C.S. Thom, P. Delbini, E.B. Romero, J. Zhang, I. Motta, H. Tillman, M.D. Cappellini, M. Kundu, M.J. Weiss