MOHSENIAN, SAMIN
MOHSENIAN, SAMIN
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
The genetic spectrum of rare bleeding disorders
2025 S. Mohsenian, O. Seidizadeh, A. Cairo, R. Palla, M. Menegatti, F. Peyvandi
Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database
2025 S. Mohsenian, R. Palla, M. Menegatti, A. Cairo, S.M. Siboni, M. Neerman-Arbez, M. Karimi, H. Pargantou, R. Asselta, D. Mikovic, M. Saracevic, B. Laros-van Gorkom, L. Jacobs, A. Shapiro, A. Williamson, M. Makris, A. Casini, F. Peyvandi
The thrombotic paradox in congenital fibrinogen deficiencies: from pathophysiology to practice
2025 S. Mohsenian, A. Casini, F. Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database
2024 S. Mohsenian, R. Palla, M. Menegatti, A. Cairo, A. Lecchi, A. Casini, M. Neerman-Arbez, R. Asselta, S. Scardo, S.M. Siboni, J. Blatny, O. Zapletal, J. Schved, M. Giansily-Blaizot, S. Halimeh, M.A. Daoud, H. Platokouki, H. Pergantou, R.E.G. Schutgens, M. Van Haaften-Spoor, P. Brons, B. Laros-van Gorkom, E. Van Pinxten, M. Borhany, N. Fatima, D. Mikovic, M. Saracevic, G.N. Özdemir, Y. Ay, M. Makris, C. Lockley, A. Mumford, A. Harvey, S. Austin, A. Shapiro, A. Williamson, C. Mcguinn, I. Goldberg, P. De Moerloose, F. Peyvandi
Rare inherited coagulation disorders: no longer orphan and neglected
2024 S. Mohsenian, P.M. Mannucci, M. Menegatti, F. Peyvandi
Exploring nonreplacement therapies’ impact on hemophilia and other rare bleeding disorders
2024 F. Peyvandi, O. Seidizadeh, S. Mohsenian, I. Garagiola
Diagnostic utility of bleeding assessment tools in congenital fibrinogen deficiencies
2023 S. Mohsenian, O. Seidizadeh, R. Palla, M. Jazebi, A. Azarkeivan, S. Moazezi, M.R. Baghaipour, M. Menegatti, F. Peyvandi