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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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