Siboni Simona Maria (Simona M Siboni, S M Siboni, Simona Maria Siboni)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 12

Top Topics

End Stage Renal Disease

Patient Reported

Top Venues

Haemophilia : the official journal of the World Federation of Hemophilia

Journal of clinical medicine

European journal of haematology

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

Publications

Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Siboni Simona Maria, Jan Blatny, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Mohamad Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E G Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael P Makris, Caryl Lockley, Andrew D Mumford, Andrew Harvey, Steve Austin, Amy Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. Blood advances 8 (6) (2024)
Omid Seidizadeh, Luca Mollica, Serena Zambarbieri, Luciano Baronciani, Andrea Cairo, Paola Colpani, Giovanna Cozzi, Maria Teresa Pagliari, Alessandro Ciavarella, Siboni Simona Maria, Flora Peyvandi
Type 2M/2A von Willebrand disease: a shared phenotype between type 2M and 2A. Blood advances 8 (7) (2024)
Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Siboni Simona Maria, Jan Blatny, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Mohamad Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E G Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael P Makris, Caryl Lockley, Andrew D Mumford, Andrew Harvey, Steve Austin, Amy Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. Blood advances 8 (6) (2024)
Omid Seidizadeh, Luca Mollica, Serena Zambarbieri, Luciano Baronciani, Andrea Cairo, Paola Colpani, Giovanna Cozzi, Maria Teresa Pagliari, Alessandro Ciavarella, Siboni Simona Maria, Flora Peyvandi
Type 2M/2A von Willebrand disease: A shared phenotype between type 2M and 2A. Blood advances (2024)
Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Siboni Simona Maria, Jan Blatný, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E G Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta A P Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael P Makris, Caryl Lockley, Andrew D Mumford, Andrew Harvey, Steven Kenneth Austin, Amy D Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. Blood advances (2024)
Omid Seidizadeh, Luca Mollica, Serena Zambarbieri, Luciano Baronciani, Andrea Cairo, Paola Colpani, Giovanna Cozzi, Maria Teresa Pagliari, Alessandro Ciavarella, Siboni Simona Maria, Flora Peyvandi
Type 2M/2A von Willebrand disease: a shared phenotype between type 2M and 2A. Blood advances 8 (7) (2024)
Chiara Suffritti, Roberta Gualtierotti, Sara Arcudi, Alessandro Ciavarella, Cristina Novembrino, Anna Lecchi, Silvia La Marca, Lidia Padovan, Erica Scalambrino, Marigrazia Clerici, Patrizia Bono, Ferruccio Ceriotti, Antonio Muscatello, Siboni Simona Maria, Flora Peyvandi
Characterization of Immunogenicity and Safety of COVID-19 mRNA-1273 in HIV-Positive Italian Patients with Hemophilia: A Prospective Single-Center Cohort Study. Journal of clinical medicine 12 (17) (2023)
Giancarlo Castaman, Alessandra Borchiellini, Antonio Coppola, Dorina Cultrera, Renato Marino, Augusto B Federici, Anna Chiara Giuffrida, Emanuela Marchesini, Angelo Claudio Molinari, Siboni Simona Maria, Ezio Zanon
Use of the von Willebrand factor concentrate with low factor VIII content to manage patients with inherited von Willebrand disease requiring surgical or secondary long-term prophylaxis: An expert opinion paper from an Italian panel. European journal of haematology 109 (2) (2022)
Omid Seidizadeh, Luciano Baronciani, Maria Teresa Pagliari, Giovanna Cozzi, Paola Colpani, Andrea Cairo, Siboni Simona Maria, Eugenia Biguzzi, Flora Peyvandi
Phenotypic and genetic characterizations of the Milan cohort of von Willebrand disease type 2. Blood advances 6 (13) (2022)
Maria Teresa Pagliari, Luciano Baronciani, Chiara Cordiglieri, Paola Colpani, Giovanna Cozzi, Siboni Simona Maria, Flora Peyvandi
The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patients. Haemophilia : the official journal of the World Federation of Hemophilia 28 (2) (2022)
Maria Teresa Pagliari, L Baronciani, Francesca Stufano, P Colpani, Siboni Simona Maria, Flora Peyvandi
Differential diagnosis between type 2A and 2B von Willebrand disease in a child with a previously undescribed de novo mutation. Haemophilia : the official journal of the World Federation of Hemophilia 24 (4) (2018)
Eugenia Biguzzi, Siboni Simona Maria, Flora Peyvandi
Acquired Von Willebrand syndrome and response to desmopressin. Haemophilia : the official journal of the World Federation of Hemophilia 24 (1) (2017)