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December 2018 - Volume 29 - Issue 8
pp: 663-719


Molecular genetic diagnosis of Tunisian Glanzmann thrombasthenia patients reveals a common nonsense mutation in the ITGA2B gene that seems to be specific for the studied population

Aloui, Chaker; Chakroun, Tahar; Granados, Viviana; More

Blood Coagulation & Fibrinolysis. 29(8):689-696, December 2018.


Low-dose, short course alteplase treatment of submassive pulmonary embolism: a case series from the National Institutes of Health Clinical Center

Lozier, Jay N.; Elinoff, Jason M.; Suffredini, Anthony F.; More

Blood Coagulation & Fibrinolysis. 29(8):701-707, December 2018.