FASULO, MARIA ROSARIA
FASULO, MARIA ROSARIA
Universita' degli Studi di MILANO
The ISTH Bleeding Assessment Tool and the risk of future bleeding
2018 M.R. Fasulo, E. Biguzzi, M. Abbattista, F. Stufano, M.T. Pagliari, I. Mancini, M.M. Gorski, A. Cannavò, M. Corgiolu, F. Peyvandi, F.R. Rosendaal
Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients
2016 M.M. Gorski, K. Blighe, L.A. Lotta, E. Pappalardo, I. Garagiola, I. Mancini, M.E. Mancuso, M.R. Fasulo, E. Santagostino, F. Peyvandi
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
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
The thrombin generation assay distinguishes inhibitor from non-inhibitor patients with severe haemophilia A
2016 M. Mancuso, V. Chantarangkul, M. Clerici, M. Fasulo, L. Padovan, E. Scalambrino, F. Peyvandi, A. Tripodi, E. Santagostino
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
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
Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity : the OPTIMAL CARE study
2010 A.T. Taher, K.M. Musallam, M. Karimi, A. El Beshlawy, K. Belhoul, S. Daar, M.S. Saned, A.H. El Chafic, M.R. Fasulo, 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
Molecular characterization of haemoglobin variants in Lombardia
2009 C. Cesaretti, C. Refaldi, M.R. Fasulo, E. Cassinerio, A. Marcon, G. Graziadei, 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
Novel human pathological mutations. Gene symbol: HBB. Disease: haemoglobin variant
2009 C. Refaldi, C. Cesaretti, M.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
Thalassemia intermedia registry
2008 A. Taher, A.H. El Chafic, M. Karimi, A. El Beshlawy, K. Belhoul, S. Daar, P. Pattoneri, R. Fasulo, M. Salah, 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
Presentazione clinica e gestione terapeutica della crisi falcemica in un reparto di Medicina Interna
2008 S. Colombo, M.R. Fasulo, P. Proto, F. Cantoni, F. Minonzio, C. Hu, G. Fabio, 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
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
Endocrine complications in beta-thalassemia populations
2008 C. Cesaretti, M. Baldini, T. Benedetta, A. Orsatti, S. Forti, M.R. Fasulo, M.D. Cappellini
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