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
2021-05-01 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
Activin receptor-ligand trap for the treatment of β-thalassemia : a serendipitous discovery
2020-11-01 V. Brancaleoni, I. Nava, P. Delbini, L. Duca, I. Motta
The autophagy-activating kinase ULK1 mediates clearance of free α-globin in β-thalassemia
2019-08-21 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
Gene symbol : G6PD. Disease : Glucose-6-phosphate dehydrogenase deficiency
2008-10-01 P. Delbini, L. Duca, I. Nava, D. Tavazzi, M.D. Cappellini
Gene symbol : HAMP. Disease : Haemochromatosis, juvenile
2008-10-01 P. Delbini, L. Duca, I. Nava, A. Meo, M.D. Cappellini
Genetic variability of TMPRSS6 and its association with iron deficiency anaemia
2010-11-01 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
2010-06-01 P. Delbini, V. Vaja, G. Graziadei, C. Cesaretti, I. Motta, M.D. Cappellini
A giant adrenal myelolipoma in a beta-thalassemia major patient : Does ineffective erythropoiesis play a role?
2016-06-10 I. Motta, L. Boiocchi, P. Delbini, M. Migone De Amicis, E. Cassinerio, D. Dondossola, G. Rossi, M.D. Cappellini
Hepcidin mutation in a beta-thalassemia major patient with persistent severe iron overload despite chelation therapy
2010-02-01 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
2008-01-01 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
2009-09-01 L. Duca, P. Delbini, I. Nava, V. Vaja, G. Fiorelli, M.D. Cappellini
New epidemiology of Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Italy
2011-10-01 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
2012-01-01 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)
2007-01-01 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
2005-05-01 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
2007-01-01 P. Delbini
Terapia combinata con deferxamina e deferiprone nel trattamento delle complicanze cardiache in un paziente affetto da grave emocromatosi giovanile
2005-10-01 G. Fabio, F. Minonzio, P. Delbini, M.D. Cappellini