FASULO, MARIA ROSARIA
FASULO, MARIA ROSARIA
Universita' degli Studi di MILANO
A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients : evidence for a founder effect
2016 I. Garagiola, S. Seregni, M. Mortarino, M.E. Mancuso, M.R. Fasulo, L.D. Notarangelo, F. Peyvandi
Absence of cardiac siderosis despite hepatic iron overload in Italian patients with thalassemia intermedia : an MRI T2* study
2010 A. Roghi, M. D. Cappellini, J. C. Wood, K. M. Musallam, P. Patrizia, M. R. Fasulo, C. Cesaretti, A. T. Taher
Bone mineralization in patients with beta-thalassemia intermedia (TI)
2008 M. Baldini, B. Tampieri, S. Forti, M.R. Fasulo, C. Cesaretti, L. Zanaboni, M.D. Cappellini
Bone mineralization in patients with beta-thalassemia intermedia (TI)
2008 I.M. Baldini, B. Tampieri, S. Forti, F.M. Ulivieri, M.R. Fasulo, C. Cesaretti, A. Marcon, E. Cassinerio, L. Zanaboni, M.D. Cappellini
Endocrine complications in beta-thalassemia populations
2008 C. Cesaretti, M. Baldini, T. Benedetta, A. Orsatti, S. Forti, M.R. Fasulo, M.D. Cappellini
Fenotipo di talassemia intermedia (TI) in soggetti eterozigoti per mutazioni del gene beta-globinico e riarrangiamenti sul cluster alfa-globinico
2008 C. Refaldi, C. Cesaretti, M.R. Fasulo, C.L. Harteveld, P.C. Giordano, M.D. Cappellini
HCC nei pazienti talassemici : l’esperienza del centro anemie congenite di Milano
2008 F. Cantoni, M.R. Fasulo, C. Cesaretti, I. Motta, E. Cassinerio, L. Zanaboni, C. Hu, G. Fabio, M.D. Cappellini
Hypercoagulability in splenectomized thalassemic patients detected by whole-blood thromboelastometry, but not by thrombin generation in platelet-poor plasma
2009 A. Tripodi, M.D. Cappellini, V. Chantarangkul, L. Padovan, M.R. Fasulo, A. Marcon, P.M. Mannucci
Interferon lambda 3 rs12979860 polymorphism in patients with haemophilia and HCV infection : a predictor of spontaneous viral clearance and sustained virological response
2014 M.E. Mancuso, S. Linari, A. Aghemo, D. Bartolozzi, E. Santagostino, M.G. Rumi, E. Fognani, M.R. Fasulo, L. Gragnani, R. Bruno, M. Morfini, A.L. Zignego, M. Colombo
La doppia eterozigosi HBS/HBC : un problema emergente
2008 M.R. Fasulo, C. Cesaretti, E. Cassinerio, L. Zanaboni, I. Motta, S. Colombo, M.D. Cappellini
Liver and heart iron overload extimated by T2* magnetic resonance (MRI T2*) in patients with thalassemia intermedia (TI)
2008 M.R. Fasulo, M.D. Cappellini, C. Cesaretti, E. Cassinerio, P. Proto, P. Pedrotti, S. Pedretti, S. Dellegrottaglie, A. Roghi
Liver and heart iron overload extimated by T2* magnetic resonance (MRI T2*) in patients with thalassemia intermedia (TI)
2008 M.R. Fasulo, C. Cesaretti, M.D. Cappellini, E. Cassinerio, P. Proto, P. Pedrotti, S. Pedretti, S. Dellegrottaglie, A. Roghi
Liver fibrosis in adult thalassemia intermedia (TI) patients assessed by transient elastography (TE)
2008 M.R. Fasulo, M. Fraquelli, C. Cesaretti, C. Rigamonti, E. Cassinerio, M.D. Cappellini
Liver fibrosis in adult thalassemia intermedia (TI) patients assessed by transient elestography (TE)
2008 M.R. Fasulo, M. Fraquelli, C. Cesaretti, A. Roghi, E. Cassinerio, C. Rigamonti, M.D. Cappellini
Liver fibrosis in adult thalassemia patients assessed by transient elastography
2008 E. Cassinerio, M. Fraquelli, M. Fasulo, C. Cesaretti, P. Pattoneri, C. Rigamonti, D. Conte, M.D. Cappellini
Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agents
2016 M.E. Mancuso, V. Chantarangkul, M. Clerici, M.R. Fasulo, L. Padovan, E. Scalambrino, F. Peyvandi, A. Tripodi, E. Santagostino
Molecular characterization of haemoglobin variants in Lombardia
2009 C. Cesaretti, C. Refaldi, M.R. Fasulo, E. Cassinerio, A. Marcon, G. Graziadei, M.D. Cappellini
Molecular heterogeneity of variegate porphyria in Italy
2008 S. Ausenda, E. Di Pierro, V. Brancaleoni, V. Besana, E. Patti, D. Tavazzi, R. Fasulo, M.D. Cappellini
Novel human pathological mutations. Gene symbol : HBA2. Disease : Thalassemia alpha
2009 C. Refaldi, M.R. Fasulo, C. Cesaretti, M.D. Cappellini
Novel human pathological mutations. Gene symbol : HMBS. Disease : porphyria, acute intermittent
2009 E. Di Pierro, V. Besana, V. Brancaleoni, M.R. Fasulo, C. Cesaretti, M.D. Cappellini