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Thrombosis and Haemostasis|May 6, 2020
Functional Fibrinolysis Assays Reveal Different Mechanisms underlying Plasminogen Dysfunction in Ligneous ConjunctivitisMarie-Charlotte Bourrienne, Stéphane Loyau, Dorothée Faille, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 30, 2022
Clinical, biological, and genetic features in an afibrinogenemia patient series in AlgeriaSoraya Hadjali-Saichi, Philippe de Mazancourt, Jacqueline Tapon-Bretaudière, et al.
Journal of Andrology|April 12, 2012
The high frequency of sperm aneuploidy in klinefelter patients and in nonobstructive azoospermia is due to meiotic errors in euploid spermatocytesFrançois Vialard, Marc Bailly, Habib Bouazzi, et al.
Plos One|September 24, 2014
Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization (IVF) ProgramsRadia Boudjenah, Denise Molina-Gomes, Antoine Torre, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 4, 2022
Reinvestigation of unidentified causative variants in FXI-deficient patients: Focus on gene segment deletionsPhilippe De Mazancourt, Annie Harroche, Katia Pouymayou, et al.
Haematologica|April 5, 2011
The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (A{alpha}Cys36Gly, A{alpha}Cys36Arg and A{alpha}Cys45Tyr) confirms the role of N-terminal A{alpha} disulfide bonds in protein assembly and secretionMichel Hanss, Catherine Pouymayou, Marie-Thérèse Blouch, et al.
Plos One|January 21, 2011
TWEAK appears as a modulator of endometrial IL-18 related cytotoxic activity of uterine natural killersMarie Petitbarat, Mona Rahmati, Valérie Sérazin, et al.
Genetic Testing|December 20, 2002
A simplified method for the detection of Y chromosome microdeletions in infertile men using a multiplex sequence-tagged site-based amplificationChristine Charpenel, Anne-Sophie Guillon, Olivier Dorson, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 12, 2006
Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiencyFlorence Quélin, Florence Mathonnet, Catherine Potentini-Esnault, et al.
Andrologia|October 27, 2020
Structural analysis of the impact of a novel androgen receptor gene mutation in two adult patients with mild androgen insensitivity syndromeMirella Hage, Delphine Drui, Bruno Francou, et al.
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