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Comparison of two hemodialysis membranes, polyacrylonitrile and cellulose acetate, on complement and coagulation systems Moll, Solange; De Moerloose, Philippe; Reber, G; Schifferli, J; Leski, Michel 1990
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Molecular etiology of factor VIII deficiency in hemophilia A Antonarakis, Stylianos; Kazazian, H. H.; Gitschier, J.; Hutter, P.; ... Morris, Michael Andréw 1995
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Prevalence of anticardiolipin and antinuclear antibodies in an elderly hospitalized population and mortality after a 6-year follow-up De Moerloose, Philippe; Boehlen, Françoise; Reber, Guido; Dechevrens, O.; ... Michel, Jean-Pierre 1997
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Measurement of plasma D-dimer is not useful in the prediction or diagnosis of postoperative deep vein thrombosis in patients undergoing total knee arthroplasty Bounameaux, Henri; Miron, Marie-José; Blanchard, J; De Moerloose, Philippe; ... Leyvraz, P F 1998
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Induction of immune tolerance with recombinant factor VIII in haemophilia A patients with inhibitors Batlle, J; Lopez, M F; Brackmann, H H; Gaillard, S; ... Stieltjes, N 1999
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Massive thromboembolism due to transcatheter ASD closure with ASDOS device Khatchatourov, Gregory; Kalangos, Afksendiyos; Anwar, Asif; Urban, Philippe; ... Faidutti, Bernard 1999
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Interaction of Anti-Phospholipid Antibodies With Late Endosomes of Human Endothelial Cells Galve-de Rochemonteix, Béatrix; Kobayashi, Toshihide; Rosnoblet, Corinne; Lindsay, Margaret; ... De Moerloose, Philippe 2000
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Inability of serial fibrin monomer measurements to predict or exclude deep venous thrombosis in asymptomatic patients undergoing total knee arthroplasty Reber, G; Blanchard, J; Bounameaux, Henri; Hoffmeyer, Pierre; ... De Moerloose, Philippe 2000
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Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia Neerman Arbez, Marguerite; De Moerloose, Philippe; Bridel, C.; Honsberger, A.; ... Morris, Michael Andréw 2000
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Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T Attanasio, Catia; De Moerloose, Philippe; Antonarakis, Stylianos; Morris, Michael Andréw; Neerman Arbez, Marguerite 2001
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Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes Neerman Arbez, Marguerite; De Moerloose, Philippe; Honsberger, A.; Parlier, G.; ... Morris, Michael Andréw 2001
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Aerosolized iloprost induces a mild but sustained inhibition of platelet aggregation Beghetti, Maurice; Reber, Guido; De Moerloose, Philippe; Vadas, Laszlo; ... Rimensberger, Peter 2002
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Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion Vu, Dung; Bolton-Maggs, P. H.; Parr, J. R.; Morris, Michael Andréw; ... Neerman Arbez, Marguerite 2003
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Rofecoxib interaction with oral anticoagulant acenocoumarol Girardin, François; Siegenthaler, Michèle Andrée; De Moerloose, Philippe; Desmeules, Jules Alexandre 2003
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Severe factor XI deficiency in a Lebanese family: identification of a novel missense mutation (Trp501Cys) in the catalytic domain De Moerloose, Philippe; Germanos-Haddad, Myrna; Boehlen, Françoise; Neerman Arbez, Marguerite 2004
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Purpura fulminans in a child as a complication of chickenpox infection Campanelli, Alexandre; Kaya, Guerkan; Ozsahin, Ayse Hulya; La Scala, Giorgio; ... Saurat, Jean-Hilaire 2004
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Presence of autoantibodies to apolipoprotein A-1 in patients with acute coronary syndrome further links autoimmunity to cardiovascular disease Vuilleumier, Nicolas; Reber, Guido; James, Richard William; Burger, Danielle; ... Mach, François 2004
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Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells Neerman Arbez, Marguerite; Germanos-Haddad, Myrna; Tzanidakis, Konstantinos; Vu, Dung; ... De Moerloose, Philippe 2004
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Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion Vu, Dung; De Moerloose, Philippe; Batorova, A.; Lazur, J.; ... Neerman Arbez, Marguerite 2005
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Homozygosity for a Thr575Met missense mutation in the catalytic domain associated with factor XI deficiency Germanos-Haddad, Myrna; De Moerloose, Philippe; Boehlen, Françoise; Peyvandi, Flora; Neerman Arbez, Marguerite 2005
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Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia Vu, Dung; Di Sanza, Corinne; Caille, Dorothee; De Moerloose, Philippe; ... Neerman Arbez, Marguerite 2005
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Fluvastatin increases the expression of adhesion molecules, monocyte chemoattractant protein-1 and tissue factor in HUVEC stimulated by patient IgG fractions containing antiphospholipid antibodies Geindre, Sylvie Françoise; Dimitrova-tirefort, Yordanka; Fish, Richard; Satta, Nathalie; ... De Moerloose, Philippe 2005
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Anti-protein S antibodies following a varicella infection: detection, characterization and influence on thrombin generation Regnault, V; Boehlen, Françoise; Ozsahin, Ayse Hulya; Wahl, Denys; ... De Moerloose, Philippe 2005
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Combined factor V - factor VIII deficiency (F5F8D): compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patient Farah, R. A.; De Moerloose, Philippe; Bouchardy, Isabelle; Morris, Michael Andréw; ... Neerman Arbez, Marguerite 2006
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Anticoagulation orale et pharmacogénétique : perspectives pour la pratique clinique Benusiglio, Patrick Raphaël; Desmeules, Jules Alexandre; De Moerloose, Philippe; Dayer, Pierre 2007
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Immunization of LDL receptor-deficient mice with beta2-glycoprotein 1 or human serum albumin induces a more inflammatory phenotype in atherosclerotic plaques Geindre, Sylvie Françoise; Kwak, Brenda; Pelli, Graziano; Roth, Isabelle; ... De Moerloose, Philippe 2007
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Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations Neerman Arbez, Marguerite; De Moerloose, Philippe 2007
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A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis Robert-Ebadi, Helia; Le Querrec, Agnès; De Moerloose, Philippe; Gandon-Laloum, Sylvie; ... Neerman Arbez, Marguerite 2008
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Induction of TLR2 expression by inflammatory stimuli is required for endothelial cell responses to lipopeptides Satta, Nathalie; Kruithof, Egbert; Reber, Guido; De Moerloose, Philippe 2008
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Chapter 12 Blood coagulation and fibrinolysis: mechanisms of thrombosis De Moerloose, Philippe; Boehlen, Françoise 2008
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Technical aspects in laboratory testing for antiphospholipid antibodies: is standardization an impossible dream? Reber, Guido; Boehlen, Françoise; De Moerloose, Philippe 2008
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Endothelial cell activation by immunoglobulins from patients with immune thrombocytopenic purpura or with antiphospholipid syndrome Geindre, Sylvie Françoise; Boehlen, Françoise; Favier, Remi; Wahl, Denis; ... De Moerloose, Philippe 2008
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Deletion of 3 residues from the C-terminus of MCFD2 affects binding to ERGIC-53 and causes combined factor V and factor VIII deficiency Nyfeler, Beat; Kamiya, Yukiko; Boehlen, Françoise; Yamamoto, Kazuo; ... Neerman Arbez, Marguerite 2008
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Aspirin response variability assessed with the PFA-100 device Reny, Jean-Luc; Quéré, Isabelle; De Moerloose, Philippe; Fontana, Pierre 2008
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A multicenter evaluation of a new quantitative highly sensitive D-dimer assay for exclusion of venous thromboembolism De Moerloose, Philippe; Palareti, Gualtiero; Aguilar, Carlos; Legnani, Cristina; ... Peetz, Dirk 2008
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Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlation Djambas Khayat, C.; Salem, N.; Chouery, E.; Corbani, S.; ... Mégarbané, A. 2008
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Mécanismes d'activation cellulaire par les anticorps antiphospholipides Satta, Nathalie; Kruithof, Egbert; Reber, Guido; De Moerloose, Philippe 2008
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Preventing and treating bleeding complications: new insights into therapeutic options De Moerloose, Philippe; Négrier, Claude 2008
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Invitation to a debate on the serological criteria that define the antiphospholipid syndrome Galli, M.; Reber, Guido; De Moerloose, Philippe; de Groot, P G. 2008
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Rare bleeding disorders Peyvandi, F.; Cattaneo, M.; Inbal, A.; De Moerloose, Philippe; Spreafico, M. 2008
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Treatment of congenital fibrinogen disorders De Moerloose, Philippe; Neerman Arbez, Marguerite 2008
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Use of the PFA-100 closure time to predict cardiovascular events in aspirin-treated cardiovascular patients: a systematic review and meta-analysis Reny, Jean-Luc; De Moerloose, Philippe; Dauzat, M.; Fontana, Pierre 2008
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Aspirin "resistance" and risk of cardiovascular morbidity Fontana, Pierre; De Moerloose, Philippe; Gris, J-C.; Reny, Jean-Luc 2008
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Assessing aspirin responsiveness using the Verify Now Aspirin assay Fontana, Pierre; Reber, Guido; De Moerloose, Philippe 2008
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D-Dimer for venous thromboembolism diagnosis: 20 years later Righini, M.; Perrier, Arnaud; De Moerloose, Philippe; Bounameaux, Henri 2008
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A survey of adherence to haemophilia therapy in six European countries: results and recommendations De Moerloose, Philippe; Urbancik, W.; Van Den Berg, H M.; Richards, M. 2008
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A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream Robert-Ebadi, Helia; De Moerloose, Philippe; El Khorassani, M.; El Khattab, M.; Neerman Arbez, Marguerite 2009
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Congenital fibrinogen disorders De Moerloose, Philippe; Neerman Arbez, Marguerite 2009
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Fibrinogen Krakow: a novel hypo/dysfibrinogenemia mutation in fibrinogen gamma chain (Asn325Ile) affecting fibrin clot structure and function Undas, Anetta; Zdziarska, Joanna; Iwaniec, Teresa; Stepien, Ewa; ... Neerman Arbez, Marguerite 2009
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Severe bleeding and miscarriages in a hypofibrinogenemic woman heterozygous for the gamma Ala82Gly mutation Zdziarska, Joanna; Undas, Anetta; Basa, Joanna; Iwaniec, Teresa; ... Neerman Arbez, Marguerite 2009
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