Serena Barozzi

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 6

Top Venues

Annals of hematology

Blood

Fondazione IRCCS Policlinico San Matteo

Università degli Studi di Pavia (BSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Fondazione IRCCS Policlinico San Matteo Jan 1o 2015

Italy

Research Fellow :: Internal Medicine

Education History

Università degli Studi di Pavia

Italy

BSC

Publications

Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families. Annals of hematology (2022)
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families. Annals of hematology 102 (3) (2022)
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families. Annals of hematology 102 (3) (2022)
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families. Annals of hematology 102 (3) (2022)
Serena Barozzi, Alessandro Pecci, Maddalena Marinoni, Giorgia Fontana, Melania Eva Zanchetta, Patrizia Noris, Anna Savoia, Michela Faleschini
GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families. Annals of hematology 102 (3) (2022)
Caterina Marconi, Christian A Di Buduo, Kellie LeVine, Serena Barozzi, Michela Faleschini, Valeria Bozzi, Flavia Palombo, Spencer U McKinstry, Giuseppe Lassandro, Paola Giordano, Patrizia Noris, Carlo L Balduini, Anna Savoia, Alessandra Balduini, Tommaso Pippucci, Marco Seri, Nicholas Katsanis, Alessandro Pecci
Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia. Blood 133 (12) (2018)

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Publication Activity (10 Years)

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Serena Barozzi