Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency

por Paraboschi, Elvezia Maria, Menegatti, Marzia, Peyvandi, Flora, Duga, Stefano, Asselta, Rosanna
Publicado 2019

An international registry of patients with plasminogen deficiency (HISTORY)

por Shapiro, Amy D., Menegatti, Marzia, Palla, Roberta, Boscarino, Marco, Roberson, Christopher, Lanzi, Paolo, Bowen, Joel, Nakar, Charles, Janson, Isaac A., Peyvandi, Flora
Publicado 2020

Safety and effectiveness of recombinant factor XIII‐A(2) in congenital factor XIII deficiency: Real‐world evidence

por Poulsen, Lone Hvitfeldt, Kerlin, Bryce A., Castaman, Giancarlo, Molinari, Angelo Claudio, Menegatti, Marzia, Nugent, Diane, Dey, Sohan, Garly, May‐Lill, Carcao, Manuel
Publicado 2022

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

por Guipponi, Michel, Masclaux, Frédéric, Sloan-Béna, Frédérique, Di Sanza, Corinne, Özbek, Namik, Peyvandi, Flora, Menegatti, Marzia, Casini, Alessandro, Malbora, Baris, Neerman-Arbez, Marguerite
Publicado 2021

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

por Lotta, Luca A, Wang, Mark, Yu, Jin, Martinelli, Ida, Yu, Fuli, Passamonti, Serena M, Consonni, Dario, Pappalardo, Emanuela, Menegatti, Marzia, Scherer, Steven E, Lewis, Lora L, Akbar, Humeira, Wu, Yuanqing, Bainbridge, Matthew N, Muzny, Donna M, Mannucci, Pier M, Gibbs, Richard A, Peyvandi, Flora
Publicado 2012