Population-based prevalence and mutational landscape of von Willebrand disease using large-scale genetic databases

por Seidizadeh, Omid, Cairo, Andrea, Baronciani, Luciano, Valenti, Luca, Peyvandi, Flora
Publicado 2023

Worldwide SARS-CoV-2 haplotype distribution in early pandemic

por Cairo, Andrea, Iorio, Marilena V., Spena, Silvia, Tagliabue, Elda, Peyvandi, Flora
Publicado 2022

Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor

por Spena, Silvia, Cairo, Andrea, Gianniello, Francesca, Pappalardo, Emanuela, Mortarino, Mimosa, Garagiola, Isabella, Martinelli, Ida, Peyvandi, Flora
Publicado 2023

Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A

por Spena, Silvia, Cairo, Andrea, Pappalardo, Emanuela, Gorski, Marcin M., Garagiola, Isabella, Hassan, Shermarke, Gualtierotti, Roberta, Peyvandi, Flora
Publicado 2022

Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis

por Pagliari, Maria Teresa, Cairo, Andrea, Boscarino, Marco, Mancini, Ilaria, Pappalardo, Emanuela, Bucciarelli, Paolo, Martinelli, Ida, Rosendaal, Frits R., Peyvandi, Flora
Publicado 2021

Phenotypic and genetic characterizations of the Milan cohort of von Willebrand disease type 2

por Seidizadeh, Omid, Baronciani, Luciano, Pagliari, Maria Teresa, Cozzi, Giovanna, Colpani, Paola, Cairo, Andrea, Siboni, Simona Maria, Biguzzi, Eugenia, Peyvandi, Flora
Publicado 2022

Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects

por Gorski, Marcin M., Lecchi, Anna, Femia, Eti A., La Marca, Silvia, Cairo, Andrea, Pappalardo, Emanuela, Lotta, Luca A., Artoni, Andrea, Peyvandi, Flora
Publicado 2019