GARAGIOLA, ISABELLA MARIA
GARAGIOLA, ISABELLA MARIA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Gender equity in hemophilia: need for healthcare, familial, and societal advocacy
2024 R. Gualtierotti, I. Garagiola, M. Mortarino, S. Spena, O. Romero-Lux, F. Peyvandi
Exploring nonreplacement therapies’ impact on hemophilia and other rare bleeding disorders
2024 F. Peyvandi, O. Seidizadeh, S. Mohsenian, I. Garagiola
Knowledge and attitudes toward gene therapy of a cohort of Italian patients with hemophilia
2023 I. Cutica, M. Mortarino, I. Garagiola, G. Pravettoni, F. Peyvandi
Psychological and cognitive factors involved in decision‐making process of haemophilia carriers in reproductive choices
2023 I. Cutica, M. Mortarino, I. Garagiola, G. Pravettoni, F. Peyvandi
Fitusiran in haemophilia: a breakthrough drug with many unknowns
2023 F. Peyvandi, I. Garagiola, M. Abbattista
Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A
2022 S. Spena, A. Cairo, E. Pappalardo, M.M. Gorski, I. Garagiola, S. Hassan, R. Gualtierotti, F. Peyvandi
Updates on Novel Non-Replacement Drugs for Hemophilia
2022 R. Gualtierotti, S. Pasca, A. Ciavarella, S. Arcudi, A. Giachi, I. Garagiola, C. Suffritti, S.M. Siboni, F. Peyvandi
Post-authorization pharmacovigilance for hemophilia in Europe and the USA: Independence and transparency are keys
2021 F. Peyvandi, I. Garagiola, P.M. Mannucci
Performance of a clinical risk prediction model for inhibitor formation in severe haemophilia A
2021 S. Hassan, R. Palla, C. Valsecchi, I. Garagiola, A. El-Beshlawy, M. Elalfy, V. Ramanan, P. Eshghi, M. Karimi, S.C. Gouw, P.M. Mannucci, F.R. Rosendaal, F. Peyvandi
Development of a specific monoclonal antibody to detect male cells expressing the rps4y1 protein
2021 S. Spena, C. Cordiglieri, I. Garagiola, F. Peyvandi
Immune Responses to Plasma-Derived Versus Recombinant FVIII Products
2021 F. Peyvandi, S. Miri, I. Garagiola
The EHA research roadmap: Blood coagulation and hemostatic disorders
2021 S. Eichinger, P.E. Morange, M. Cattaneo, M. Fretigny, A. Rauch, A. van Hylckama Vlieg, D.-. Tregouet, W. Ruf, M. Levi, J.A. Paramo, T. van der Poll, P.A. Kyrle, I. Garagiola, F. Peyvandi
X Chromosome inactivation: a modifier of factor VIII and IX plasma levels and bleeding phenotype in Haemophilia carriers
2020 I. Garagiola, M. Mortarino, S.M. Siboni, M. Boscarino, M.E. Mancuso, M. Biganzoli, E. Santagostino, F. Peyvandi
Real-life experience in switching to new extended half-life products at European haemophilia centres
2019 F. Peyvandi, I. Garagiola, M. Boscarino, A. Ryan, C. Hermans, M. Makris
Clinical advances in gene therapy updates on clinical trials of gene therapy in haemophilia
2019 F. Peyvandi, I. Garagiola
Molecular Aggregation of Marketed Recombinant FVIII Products: Biochemical Evidence and Functional Effects
2019 R. De Cristofaro, M. Sacco, S. Lancellotti, F. Berruti, I. Garagiola, C. Valsecchi, M. Basso, E. Di Stasio, F. Peyvandi
Prediction of Factor VIII inhibitor development in the SIPPET cohort by mutational analysis and Factor VIII antigen measurement
2018 S. Spena, I. Garagiola, A. Cannavò, M. Mortarino, P.M. Mannucci, F.R. Rosendaal, F. Payvandi, A. El-Beshlawy, M. Elalfy, V. Ramanan, P. Eshghi, S. Hanagavadi, R. Varadarajan, M. Karimi, M.V. Manglani, C. Ross, G. Young, T. Seth, S. Apte, D.M. Nayak, E. Santagostino, M.E. Mancuso, A.C. Sandoval Gonzalez, J.N. Mahlangu, S. Bonanad Boix
Timing and severity of inhibitor development in recombinant versus plasma-derived factor VIII concentrates: a SIPPET analysis
2018 F. Peyvandi, A. Cannavò, I. Garagiola, R. Palla, P.M. Mannucci, F.R. Rosendaal, A. El-Beshlawy, M. Elalfy, V. Ramanan, P. Eshghi, S. Hanagavadi, R. Varadarajan, M. Karimi, M.V. Manglani, C. Ross, G. Young, T. Seth, S. Apte, D.M. Nayak, E. Santagostino, M. Elisa Mancuso, A.C. Sandoval Gonzalez, J.N. Mahlangu, S. Bonanad Boix, M. Cerqueira, N.P. Ewing, C. Male, T. Owaidah, V. Soto Arellano, N.L. Kobrinsky, S. Majumdar, R. Perez Garrido, A. Sachdeva, M. Simpson, M. Thomas, E. Zanon, B. Antmen, K. Kavakl, M.J. Manco-Johnson, M. Martinez, E. Marzouka, M.G. Mazzucconi, D. Neme, A. Palomo Bravo, R. Paredes Aguilera, A. Prezotti, K. Schmitt, B.M. Wicklund, B. Zulfikar
Product type and other environmental risk factors for inhibitor development in severe hemophilia A
2018 F. Peyvandi, I. Garagiola
Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activity
2018 I. Donadon, J.H. Mcvey, I. Garagiola, A. Branchini, M. Mortarino, F. Peyvandi, F. Bernardi, M. Pinotti