MENEGATTI, MARZIA
MENEGATTI, MARZIA
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
Rare inherited coagulation disorders: no longer orphan and neglected
2024 S. Mohsenian, P.M. Mannucci, M. Menegatti, 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
Clinical, Laboratory Aspects and Management of Factor X Deficiency
2024 M. Menegatti, F. Peyvandi
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
A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family
2021 M. Guipponi, F. Masclaux, F. Sloan-Béna, C. Di Sanza, N. Özbek, F. Peyvandi, M. Menegatti, A. Casini, B. Malbora, M. Neerman-Arbez
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease
2020 E.M. Paraboschi, A.V. Khera, P.A. Merlini, L. Gigante, F. Peyvandi, M. Chaffin, M. Menegatti, F. Busti, D. Girelli, N. Martinelli, O. Olivieri, S. Kathiresan, D. Ardissino, R. Asselta, S. Duga
An international registry of patients with plasminogen deficiency (HISTORY)
2020 A.D. Shapiro, M. Menegatti, R. Palla, M. Boscarino, C. Roberson, P. Lanzi, J. Bowen, C. Nakar, I.A. Janson, F. Peyvandi
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency.
2019 E. Paraboschi, M. Menegatti, F. Payvandi, S. Duga, R. Asselta
Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis
2019 A.C. Weyand, S.J. Grzegorski, M.S. Rost, K.I. Lavik, A.C. Ferguson, M. Menegatti, C.E. Richter, R. Asselta, S. Duga, F. Payvandi, J.A. Shavit
Management of rare acquired bleeding disorders
2019 M. Menegatti, E. Biguzzi, F. Peyvandi
Treatment of rare factor deficiencies other than hemophilia
2019 M. Menegatti, F. Peyvandi
Recombinant factor XIII A-subunit in a patient with factor XIII deficiency and recurrent pregnancy loss
2018 M. Al-Khabori, A. Pathare, M. Menegatti, F. Payvandi
Molecular investigation of 41 patients affected by coagulation factor XI deficiency
2018 V. Rimoldi, E.M. Paraboschi, M. Menegatti, F. Peyvandi, O. Salomon, S. Duga, R. Asselta
Minimal factor XIII activity level to prevent major spontaneous bleeds : reply
2017 M. Menegatti, R. Palla, P. Bucciarelli, F. Peyvandi
Genome editing of factor X in zebrafish reveals unexpected tolerance of severe defects in the common pathway
2017 Z. Hu, Y. Liu, M.C. Huarng, M. Menegatti, D. Reyon, M.S. Rost, Z.G. Norris, C.E. Richter, A.N. Stapleton, N.C. Chi, F. Peyvandi, J.K. Joung, J.A. Shavit
Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories
2017 I. Jennings, S. Kitchen, M. Menegatti, R. Palla, I. Walker, F. Peyvandi, M. Makris
Exploring the global landscape of genetic variation in coagulation factor XI deficiency
2017 R. Asselta, E.M. Paraboschi, V. Rimoldi, M. Menegatti, F. Peyvandi, O. Salomon, S. Duga
Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO-RBDD project laboratories
2017 I. Jennings, S. Kitchen, M. Menegatti, R. Palla, I. Walker, M. Makris, F. Peyvandi