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Prevalence, persistence and clinical correlations of classic and novel antiphospholipid antibodies in systemic lupus erythematosus Marchetti, Tess; Ribi, Camillo; Perneger, Thomas; Trendelenburg, Marten; ... Chizzolini, Carlo 2018
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Mutational epidemiology of congenital fibrinogen disorders Casini, Alessandro; Blondon, Marc; Tintillier, Veronique; Goodyer, Matthew; ... Neerman Arbez, Marguerite 2018
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Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH Casini, Alessandro; Undas, A; Palla, R; Thachil, J; De Moerloose, Philippe 2018
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Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia Casini, Alessandro; Vilarino, Raquel; Beauverd, Yan; Aslan, D; ... Neerman Arbez, Marguerite 2017
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Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization Amri, Y; Jouini, H; Becheur, M; Dabboubi, R; ... Toumi, N E H 2017
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Patient-derived anti-β2GP1 antibodies recognize a peptide motif pattern and not a specific sequence of residues De Moerloose, Philippe; Fickentscher, Céline; Boehlen, Françoise; Tiercy, Jean-Marie; ... Brandt, Karim J 2017
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A multicenter study to assess the reproducibility of antiphospholipid antibody results produced by an automated system Devreese, K M; Poncet, Antoine; Lindhoff-Last, E; Musial, J; ... Fontana, Pierre 2017
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Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation Casini, Alessandro; Brungs, T; Lavenu-Bombled, C; Vilar, R; ... De Moerloose, Philippe 2017
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Preoperative hemostatic assessment: a new and simple bleeding questionnaire Bonhomme, Fanny; Boehlen, Françoise; Clergue, François; De Moerloose, Philippe 2016
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Management of congenital quantitative fibrinogen disorders: a Delphi consensus Casini, Alessandro; De Moerloose, Philippe 2016
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Congenital Disorders of Fibrinogen: Clinical Presentations, Diagnosis and Management Casini, Alessandro; De Moerloose, Philippe 2016
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Pregnancy Marchetti, T; De Moerloose, Philippe; Casini, Alessandro 2016
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Clinical Features and Management of Congenital Fibrinogen Deficiencies Casini, Alessandro; De Moerloose, Philippe; Neerman Arbez, Marguerite 2016
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Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders Neerman Arbez, Marguerite; De Moerloose, Philippe; Casini, Alessandro 2016
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Factor concentrates for rare congenital coagulation disorders: where are we now? Casini, Alessandro; De Moerloose, Philippe 2016
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Can the phenotype of inherited fibrinogen disorders be predicted? Casini, Alessandro; De Moerloose, Philippe 2016
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F-actin dampens NLRP3 inflammasome activity via Flightless-I and LRRFIP2 Burger, Danielle; Fickentscher, Céline; De Moerloose, Philippe; Brandt, Karim 2016
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Hypertension, haematuria and renal functioning in haemophilia - a cross-sectional study in Europe Holme, P. A.; Combescure, Christophe; Tait, R.C.; Berntorp, E.; ... De Moerloose, Philippe 2016
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Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management Casini, Alessandro; Neerman Arbez, Marguerite; Ariëns, R A; De Moerloose, Philippe 2015
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Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature Casini, Alessandro; Sokollik, C; Lukowski, Samuel; Lurz, E; ... Neerman Arbez, Marguerite 2015
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Recombinant human FVIIa for reducing the need for invasive second-line therapies in severe refractory postpartum hemorrhage: a multicenter, randomized, open controlled trial Lavigne-Lissalde, G; Aya, A G; Mercier, F J; Roger-Christoph, S; ... Gris, J-C 2015
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Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis Lebreton, A; Casini, Alessandro; Alhayek, R; Kouteich, K L; ... De Moerloose, Philippe 2015
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Natural history of patients with congenital dysfibrinogenemia Casini, Alessandro; Blondon, Marc; Lebreton, Aurelien; Koegel, Jeremie; ... De Moerloose, Philippe 2015
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Fibrinogen geneva II: a new congenitally abnormal fibrinogen alpha chain (Gly17Asp) with a review of similar mutations resulting in abnormal knob A. Casini, Alessandro; De Maistre, Emmanuel; Casini-Stuppi, Virginie; Fontana, Pierre; ... De Moerloose, Philippe 2014
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Evaluation of the GEM®PCL Plus point-of-care device for neonatal coagulation assessment: An observational study on cord blood De Luca, Roberta; Fontana, Pierre; Poncet, Antoine; De Moerloose, Philippe; Pfister, Riccardo 2014
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FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations Casini, Alessandro; Lukowski, Samuel; Quintard, V Louvain; Crutu, A; ... Neerman Arbez, Marguerite 2014
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NF-κB is activated from endosomal compartments in antiphospholipid antibodies-treated human monocytes Brandt, Karim; Fickentscher, Céline; Boehlen, Françoise; Kruithof, Egbert; De Moerloose, Philippe 2014
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Hydroxychloroquine restores trophoblast fusion affected by antiphospholipid antibodies Marchetti, Tess; Ruffatti, A.; Wuillemin-Rambosson, Christine Gabrielle; De Moerloose, Philippe; Cohen, Marie-Benoîte 2014
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Refinement of the cutoff values of the HemosIL AcuStar assay for the detection of anticardiolipin and anti-beta2 glycoprotein-1 antibodies Fontana, Pierre; Poncet, Antoine; Lindhoff-Last, E; De Moerloose, Philippe; Devreese, K M 2014
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Hémostase : nouveaux anticoagulants oraux : de la théorie à la pratique De Moerloose, Philippe; Casini, Alessandro; Boehlen, Françoise; Fontana, Pierre 2013
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TLR2 ligands induce NF-κB activation from endosomal compartments of human monocytes Brandt, Karim; Fickentscher, Céline; Kruithof, Egbert; De Moerloose, Philippe 2013
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Receptors involved in cell activation by antiphospholipid antibodies Brandt, Karim; Kruithof, Egbert; De Moerloose, Philippe 2013
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Diagnosis and management of obstetrical antiphospholipid syndrome: where do we stand? Marchetti, Tess; Cohen, Marie-Benoîte; Gris, Jean-Christophe; De Moerloose, Philippe 2013
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Obstetrical Antiphospholipid Syndrome: From the Pathogenesis to the Clinical and Therapeutic Implications Marchetti, Tess; Cohen, Marie-Benoîte; De Moerloose, Philippe 2013
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Could Factor XIII be a solution for the management of surgical bleeding? Casini, Alessandro; De Moerloose, Philippe 2013
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Pulmonary embolism and fatal stroke in a patient with severe factor XI deficiency after bariatric surgery Boehlen, Françoise; Casini, Alessandro; Pugin, François Louis; De Moerloose, Philippe 2013
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Acquired factor XIII deficiency: a therapeutic challenge Boehlen, Françoise; Casini, Alessandro; Chizzolini, Carlo; Mansouri, Behrouz; ... De Moerloose, Philippe 2013
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Congenital fibrinogen disorders: an update De Moerloose, Philippe; Casini, Alessandro; Neerman Arbez, Marguerite 2013
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Identification of a novel F11 missense mutation (Ile463Ser) in a family with congenital factor XI deficiency Tirefort, Yordanka; Uhr, Mario R; Neerman Arbez, Marguerite; De Moerloose, Philippe 2012
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Antiplatelet drug response status does not predict recurrent ischemic events in stable cardiovascular patients: results of the Antiplatelet Drug Resistances and Ischemic Events study Reny, Jean-Luc; Berdagué, Philippe; Poncet, Antoine; Barazer, Isabelle; ... Fontana, Pierre 2012
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Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia Tirefort, Yordanka; Alson, Olivat Rakoto; De Moerloose, Philippe; Neerman Arbez, Marguerite 2012
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Thrombophilie : quel bilan en 2012? De Moerloose, Philippe; Casini, Alessandro; Boehlen, Françoise 2012
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Anti-apolipoprotein A-1 IgG in patients with myocardial infarction promotes inflammation through TLR2/CD14 complex Pagano, Sabrina; Satta, Nathalie; Werling, D; Offord, Valérie Edna; ... Vuilleumier, Nicolas 2012
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Inflammatory and prothrombotic states in obese children of European descent Stoppa-Vaucher, Sophie; Dirlewanger, Mirjam A; Meier, Christoph; De Moerloose, Philippe; ... Schwitzgebel Luscher, Valérie 2012
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A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family Levrat, Emmanuel; Aboukhamis, Imad; De Moerloose, Philippe; Farho, Jaafar; ... Neerman Arbez, Marguerite 2011
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Platelet reactivity is a stable and global phenomenon in aspirin-treated cardiovascular patients Zufferey Bakos, Anne; Reny, Jean-Luc; Combescure, Christophe; De Moerloose, Philippe; ... Fontana, Pierre 2011
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Toll-like receptor 2 mediates the activation of human monocytes and endothelial cells by antiphospholipid antibodies Poschung, Nathalie; Kruithof, Egbert; Fickentscher, Céline; Geindre, Sylvie Françoise; ... De Moerloose, Philippe 2011
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Thromboprophylaxis with low-molecular-weight heparin after cesarean delivery Blondon, Marc; Perrier, Arnaud; Nendaz, Mathieu; Righini, Marc Philip; ... De Moerloose, Philippe 2010
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Identification and functional characterization of a novel nonsense mutation in FGA accounting for congenital afibrinogenemia in six Egyptian patients Abdel Wahab, Magy; De Moerloose, Philippe; Fish, R. J.; Neerman Arbez, Marguerite 2010
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Fibrinogen and the risk of thrombosis De Moerloose, Philippe; Boehlen, Françoise; Neerman Arbez, Marguerite 2010
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