A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene

por Mansory, Eman M., Bhai, Pratibha, Stuart, Alan, Laudenbach, Lori, Sadikovic, Bekim, Lazo‐Langner, Alejandro
Publicado 2021

From the voices of people with haemophilia A and their caregivers: Challenges with current treatment, their impact on quality of life and desired improvements in future therapies

por Wiley, Ryan E., Khoury, Charles P., Snihur, Adrian W. K., Williams, Marni, Page, David, Graham, Nicole, Laudenbach, Lori, Milne‐Wren, Cindy, Stoffman, Jayson M.
Publicado 2019