Showing results (331-340 of 867) with videos related to
Sort By:
Pageof 87
The Journal of Biological Chemistry|December 22, 2011
A high affinity interaction of plasminogen with fibrin is not essential for efficient activation by tissue-type plasminogen activatorPaul Y Kim, Long D Tieu, Alan R Stafford, et al.Thrombosis and Haemostasis|April 21, 2019
Factor XIII Prevents Pulmonary Emboli in Mice by Stabilizing Deep Vein ThrombiShana A Shaya, Dhulfiha Muzafar Gani, Jeffrey I Weitz, et al.International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|April 21, 2015
Mediterranean spotted fever and hearing impairment: a rare complicationRaffaella Rossio, Valeria Conalbi, Valentina Castagna, et al.Haematologica|September 2, 2004
Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domainGiovanna D'Andrea, Anna Bossone, Maria Rosaria Lupone, et al.Thrombosis Research|November 6, 2019
The features of acquired thrombotic thrombocytopenic purpura occurring at advanced agePasquale Agosti, Ilaria Mancini, Andrea Artoni, et al.Journal of Thrombosis and Haemostasis : JTH|December 28, 2020
Characterization of the neutralizing anti-emicizumab antibody in a patient with hemophilia A and inhibitorCarla Valsecchi, Marco Gobbi, Marten Beeg, et al.Thrombosis Research|January 8, 2014
A recurrent Gly43Asp substitution in coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular traffickingMarzia Menegatti, Anna Vangone, Roberta Palla, et al.Molecular Genetics & Genomic Medicine|April 12, 2016
A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effectIsabella Garagiola, Sabrina Seregni, Mimosa Mortarino, et al.Haematologica|November 25, 2017
Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activityIrving Donadon, John H McVey, Isabella Garagiola, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|August 4, 2022
Analysis of fibrinogen concentrate pharmacokinetics and dosing for bleeds and surgery in adults, adolescents, and children with congenital afibrinogenaemia and hypofibrinogenaemiaClaudia Djambas Khayat, Sunil D Lohade, Omid R Zekavat, et al.Pageof 87