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Hamostaseologie|March 12, 2025
Congenital Fibrinogen Deficiencies: Not So RareAlexander Couzens, Marguerite Neerman-ArbezBlood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 5, 2023
Coexpression of factor VIII and factor von Willebrand variants in a woman with heavy menstrual bleedingAlessandro Casini, Michal Yaron, Alexander Couzens, et al.Pathophysiology of Haemostasis and Thrombosis|July 21, 2006
Molecular basis of fibrinogen deficiencyMarguerite Neerman-ArbezInternational Journal of Molecular Sciences|January 11, 2018
Clinical Consequences and Molecular Bases of Low Fibrinogen LevelsMarguerite Neerman-Arbez, Alessandro CasiniExpert Opinion on Biological Therapy|June 14, 2008
Treatment of congenital fibrinogen disordersPhilippe de Moerloose, Marguerite Neerman-ArbezThrombosis and Haemostasis|July 28, 2012
Fibrinogen gene regulationRichard J Fish, Marguerite Neerman-ArbezThrombosis and Haemostasis|July 28, 2012
A novel regulatory element between the human FGA and FGG genesRichard J Fish, Marguerite Neerman-ArbezHuman Mutation|February 14, 2007
Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutationsMarguerite Neerman-Arbez, Philippe de MoerlooseSeminars in Thrombosis and Hemostasis|July 15, 2009
Congenital fibrinogen disordersPhilippe de Moerloose, Marguerite Neerman-ArbezBlood|October 31, 2002
Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA)Catia Attanasio, Armelle David, Marguerite Neerman-ArbezPageof 9