Frequency of Immune Thrombocytopenia in Newborns: A Prospective Study von Dreyfus, Marie, Kaplan, Cécile, Verdy, Elizabeth, Schlegel, Nicole, Durand-Zaleski, Isabelle, Tchernia, Gil

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Injection of recombinant activated factor VII can induce transient increase in circulating procoagulant microparticles von Proulle, Valérie, Hugel, Bénédicte, Guillet, Benoit, Trichet, Catherine, Rafowicz, Anne, Lambert, Thierry, Freyssinet, Jean-Marie, Dreyfus, Marie

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High prevalence of the natural Asn89Asp mutation in the GP1BB gene associated with Bernard–Soulier syndrome in French patients from the genetic isolate of Reunion Island von Fiore, Mathieu, De Thoré, Céline, Randrianaivo‐Ranjatoelina, Hanitra, Baas, Marie‐Jeanne, Jacquemont, Marie‐Line, Dreyfus, Marie, Lavenu‐Bombled, Cécile, Li, Renhao, Gachet, Christian, Dupuis, Arnaud, Lanza, Francois

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Risk Factors for Thrombosis in an African Population von Fall, Awa O.T., Proulle, Valérie, Sail, Abibatou, Mbaye, Alassane, Ba, Pape Samba, Diao, Maboury, Seck, Moussa, Gadji, Macoura, Gning, Sara B., Diop, Saliou, Dièye, Tandakha N.D., Faye, Blaise Félix, Thiam, Doudou, Dreyfus, Marie

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A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture von Veyradier, Agnès, Boisseau, Pierre, Fressinaud, Edith, Caron, Claudine, Ternisien, Catherine, Giraud, Mathilde, Zawadzki, Christophe, Trossaert, Marc, Itzhar-Baïkian, Nathalie, Dreyfus, Marie, d'Oiron, Roseline, Borel-Derlon, Annie, Susen, Sophie, Bezieau, Stéphane, Denis, Cécile V, Goudemand, Jenny

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Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort von Nurden, Alan T., Pillois, Xavier, Fiore, Mathieu, Alessi, Marie-Christine, Bonduel, Mariana, Dreyfus, Marie, Goudemand, Jenny, Gruel, Yves, Benabdallah-Guerida, Schéhérazade, Latger-Cannard, Véronique, Négrier, Claude, Nugent, Diane, Oiron, Roseline d, Rand, Margaret L., Sié, Pierre, Trossaert, Marc, Alberio, Lorenzo, Martins, Nathalie, Sirvain-Trukniewicz, Peggy, Couloux, Arnaud, Canault, Mathias, Fronthroth, Juan Pablo, Fretigny, Mathilde, Nurden, Paquita, Heilig, Roland, Vinciguerra, Christine

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China’s Partnership Strategy and National Rejuvenation von McLean Dreyfus, Marie-Alice

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A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease von Veyradier, Agnès, Boisseau, Pierre, Fressinaud, Edith, Caron, Claudine, Ternisien, Catherine, Giraud, Mathilde, Zawadzki, Christophe, Trossaërt, Marc, Itzhar-Baikian, Nathalie, Dreyfus, Marie, d'Oiron, Roseline, Borel-Derlon, Annie, Susen, Sophie, Bézieau, Stéphane, Denis, Cecile, Goudemand, Jenny, von Willebrand Disease, French Reference Center For, Gris, Jean-Christophe

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Misdiagnosis of chronic thrombocytopenia in childhood von BADER-MEUNIER, Brigitte, PROULLE, Valérie, TRICHET, Catherine, DEBRAY, Dominique, GABOLDE, Martine, YVART, J, DREYFUS, Marie

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Pregnancy-Associated Thrombocytopenia Revisited: Assessment and Follow-Up of 50 Cases von Ajzenberg, Nadine, Dreyfus, Marie, Kaplan, Cécile, Yvart, Jeannine, Weill, Bernard, Tchernia, Gil

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A novel platelet-type von Willebrand disease mutation (GP1BA p.Met255Ile) associated with type 2B “Malmö/New York” von Willebrand disease von Lavenu-Bombled, Cécile, Guitton, Corinne, Dupuis, Arnaud, Baas, Marie-Jeanne, Desconclois, Céline, Dreyfus, Marie, Li, Renhao, Caron, Claudine, Gachet, Christian, Fressinaud, Edith, Lanza, François

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Fondaparinux (Arixtra∗ ) hepatotoxicity in a 6 year-old child von Orostegui, Lupe, Medejel, Nadia, Kone-Paut, Isabelle, Dreyfus, Marie, Benhamou, Dan

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Underestimation of unfractionated heparin therapy assessment due to platelet activation when using partial-draw (pediatric) citrate collection tubes von Desconclois, Céline, Eschwège, Valérie, Proulle, Valérie, Boutekedjiret, Tewfik, Dreyfus, Marie, Toulon, Pierre

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Hematological disorders related cerebral infarctions are mostly multifocal von Fagniez, Ombeline, Tertian, Gérard, Dreyfus, Marie, Ducreux, Denis, Adams, David, Denier, Christian

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Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome) von Geneviève, David, Proulle, Valérie, Isidor, Bertrand, Bellais, Samuel, Serre, Valérie, Djouadi, Fatima, Picard, Capucine, Vignon-Savoye, Capucine, Bader-Meunier, Brigitte, Blanche, Stéphane, de Vernejoul, Marie-Christine, Legeai-Mallet, Laurence, Fischer, Anne-Marie, Le Merrer, Martine, Dreyfus, Marie, Gaussem, Pascale, Munnich, Arnold, Cormier-Daire, Valérie

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Whole Blood Impedance Aggregometry: A New Tool for Severe Inherited Platelet Disorder Diagnosis? von Desconclois, Celine, Valarche, Vincent, Boutekedjiret, Tewfik, Raphael, Martine, Dreyfus, Marie, Proulle, Valerie

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Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency von Picard, Véronique, Chen, Jian-Min, Tardy, Brigitte, Aillaud, Marie-Françoise, Boiteux-Vergnes, Christine, Dreyfus, Marie, Emmerich, Joseph, Lavenu-Bombled, Cécile, Nowak-Göttl, Ulrike, Trillot, Nathalie, Aiach, Martine, Alhenc-Gelas, Martine

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Expanding the Mutation Spectrum Affecting alpha IIb beta 3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort von Nurden, Alan T, Pillois, Xavier, Fiore, Mathieu, Alessi, Marie-Christine, Bonduel, Mariana, Dreyfus, Marie, Goudemand, Jenny, Gruel, Yves, Benabdallah-Guerida, Scheherazade, Latger-Cannard, Veronique, Negrier, Claude, Nugent, Diane, Oiron, Roseline d, Rand, Margaret L, Sie, Pierre, Trossaert, Marc, Alberio, Lorenzo, Martins, Nathalie, Sirvain-Trukniewicz, Peggy, Couloux, Arnaud, Canault, Mathias, Fronthroth, Juan Pablo, Fretigny, Mathilde, Nurden, Paquita, Heilig, Roland, Vinciguerra, Christine

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Expanding the Mutation Spectrum Affecting [alpha]IIb[beta]3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort von Nurden, Alan T, Pillois, Xavier, Fiore, Mathieu, Alessi, Marie-Christine, Bonduel, Mariana, Dreyfus, Marie, Goudemand, Jenny, Gruel, Yves, Benabdallah-Guerida, Schéhérazade, Latger-Cannard, Véronique, Negrier, Claude, Nugent, Diane, Oiron, Roseline d, Rand, Margaret L, Sie, Pierre, Trossaert, Marc, Alberio, Lorenzo, Martins, Nathalie, Sirvain-Trukniewicz, Peggy, Couloux, Arnaud, Canault, Mathias, Fronthroth, Juan Pablo, Fretigny, Mathilde, Nurden, Paquita, Heilig, Roland, Vinciguerra, Christine

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THROMBOCYTOPENIA WITH ABSENT RADII (TAR SYNDROME): New Advances in the Mechanism of Thrombocytopenia von Tchernia, Marie Dreyfus, Gil

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