1-2 of 2
Britta Laros-van Gorkom
Close
Sort by
Journal Articles

Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database

Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Simona Maria Siboni, 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 Makris, Caryl Lockley, Andrew Mumford, Andrew Harvey, Steve Austin, Amy Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Journal: Blood Advances
Blood Adv (2024) 8 (6): 1392–1404.
https://doi.org/10.1182/bloodadvances.2023012186
Published: 2024
Journal Articles

The bleeding phenotype in people with nonsevere hemophilia

Fabienne R. Kloosterman, Anne-Fleur Zwagemaker, Catherine N. Bagot, Erik A. M. Beckers, Giancarlo Castaman, Marjon H. Cnossen, Peter W. Collins, Charles Hay, Michel Hof, Britta Laros-van Gorkom, Frank W. G. Leebeek, Christoph Male, Karina Meijer, Ingrid Pabinger, Susan Shapiro, Michiel Coppens, Karin Fijnvandraat, Samantha C. Gouw,
Journal: Blood Advances
Blood Adv (2022) 6 (14): 4256–4265.
https://doi.org/10.1182/bloodadvances.2022007620
Published: 2022
Includes: Supplemental data