An open conformation of ADAMTS‐13 is a hallmark of acute acquired thrombotic thrombocytopenic purpura
Roose, E., Schelpe, A. S., Joly, B. S., Peetermans, M., Verhamme, P., Voorberg, J., Greinacher, A., Deckmyn, H., De Meyer, S. F., Coppo, P., Veyradier, A., Vanhoorelbeke, K.
Published in Journal of thrombosis and haemostasis (01.02.2018)
Published in Journal of thrombosis and haemostasis (01.02.2018)
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Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies
Scully, M., Cataland, S., Coppo, P., Rubia, J., Friedman, K. D., Kremer Hovinga, J., Lämmle, B., Matsumoto, M., Pavenski, K., Sadler, E., Sarode, R., Wu, H., Gale, D., Fujimura, Y., McDonald, V., Peyvandi, F., Scharrer, I., Veyradier, A., Westwood, J. P.
Published in Journal of thrombosis and haemostasis (01.02.2017)
Published in Journal of thrombosis and haemostasis (01.02.2017)
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Journal Article
IgG subclass distribution of anti‐ADAMTS13 antibodies in patients with acquired thrombotic thrombocytopenic purpura
FERRARI, S., MUDDE, G. C., RIEGER, M., VEYRADIER, A., KREMER HOVINGA, J. A., SCHEIFLINGER, F.
Published in Journal of thrombosis and haemostasis (01.10.2009)
Published in Journal of thrombosis and haemostasis (01.10.2009)
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ADAMTS‐13 and von Willebrand factor predict venous thromboembolism in patients with cancer
Pépin, M., Kleinjan, A., Hajage, D., Büller, H. R., Di Nisio, M., Kamphuisen, P. W., Salomon, L., Veyradier, A., Stepanian, A., Mahé, I.
Published in Journal of thrombosis and haemostasis (01.02.2016)
Published in Journal of thrombosis and haemostasis (01.02.2016)
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Journal Article
HLA‐DRB111: a strong risk factor for acquired severe ADAMTS13 deficiency‐related idiopathic thrombotic thrombocytopenic purpura in Caucasians
COPPO, P., BUSSON, M., VEYRADIER, A., WYNCKEL, A., POULLIN, P., AZOULAY, E., GALICIER, L., LOISEAU, P.
Published in Journal of thrombosis and haemostasis (01.04.2010)
Published in Journal of thrombosis and haemostasis (01.04.2010)
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Journal Article
Acute renal failure is prevalent in patients with thrombotic thrombocytopenic purpura associated with low plasma ADAMTS13 activity
Zafrani, L., Mariotte, E., Darmon, M., Canet, E., Merceron, S., Boutboul, D., Veyradier, A., Galicier, L., Azoulay, E.
Published in Journal of thrombosis and haemostasis (01.03.2015)
Published in Journal of thrombosis and haemostasis (01.03.2015)
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Cardiac troponin‐I on diagnosis predicts early death and refractoriness in acquired thrombotic thrombocytopenic purpura. Experience of the French Thrombotic Microangiopathies Reference Center
Benhamou, Y., Boelle, P.‐Y., Baudin, B., Ederhy, S., Gras, J., Galicier, L., Azoulay, E., Provôt, F., Maury, E., Pène, F., Mira, J.‐P., Wynckel, A., Presne, C., Poullin, P., Halimi, J.‐M., Delmas, Y., Kanouni, T., Seguin, A., Mousson, C., Servais, A., Bordessoule, D., Perez, P., Hamidou, M., Cohen, A., Veyradier, A., Coppo, P., Elie, Azoulay, Virginie, Barbay, Guy, Bonmarchand, Dominique, Bordessoule, Christophe, Charasse, Dominique, Chauveau, Gabriel, Choukroun, Jean‐Philippe, Coindre, Paul, Coppo, Elise, Corre, Yahsou, Delmas, Georges, Deschenes, Alain, Devidas, Olivier, Fain, Véronique, Frémeaux‐Bacchi, Lionel, Galicier, Bertrand, Guidet, Jean‐Michel, Halimi, Mohamed, Hamidou, Raoul, Herbrecht, Frédéric, Jacobs, Bérangère, Joly, Tarik, Kanouni, Alexandre, Lautrette, Véronique, Le Guern, Chantal, Loirat, Jean‐Paul, Mira, Bruno, Moulin, Christiane, Mousson, Mario, Ojeda Uribe, Abdelkader, Ouchenir, Nathalie, Parquet, Julie, Peltier, Pierre, Perez, Pascale, Poullin, Claire, Pouteil‐Noble, Claire, Presne, François, Provôt, Jean‐Antoine, Ribeil, Eric, Rondeau, Samir, Saheb, Benoît, Schlemmer, Amélie, Seguin, Alain, Stépanian, Jean‐Paul, Vernant, Agnès, Veyradier, Cécile, Vigneau, François, Vrtovsnick, Alain, Wynckel, Martine, Wolf, Patricia, Zunic
Published in Journal of thrombosis and haemostasis (01.02.2015)
Published in Journal of thrombosis and haemostasis (01.02.2015)
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Venous thrombo-embolism during immune-mediated thrombotic thrombocytopenic purpura is prevalent in patients with a prolonged treatment with therapeutic plasma exchange
Benhamou, Y, Sauvètre, G, Grangé, S, Veyradier, A, Coppo, P
Published in La revue de medecine interne (01.12.2020)
Published in La revue de medecine interne (01.12.2020)
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Amplified endogenous plasmin activity resolves acute thrombotic thrombocytopenic purpura in mice
Tersteeg, C., Joly, B. S., Gils, A., Lijnen, R., Deckmyn, H., Declerck, P. J., Plaimauer, B., Coppo, P., Veyradier, A., Maas, C., De Meyer, S. F., Vanhoorelbeke, K.
Published in Journal of thrombosis and haemostasis (01.12.2017)
Published in Journal of thrombosis and haemostasis (01.12.2017)
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Journal Article
Endothelial dysfunction in thrombotic thrombocytopenic purpura: therapeutic perspectives
Prevel, R, Roubaud-Baudron, C, Tellier, E, Le Besnerais, M, Kaplanski, G, Veyradier, A, Benhamou, Y, Coppo, P
Published in La revue de medecine interne (01.03.2021)
Published in La revue de medecine interne (01.03.2021)
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Assessment of endothelial damage and cardiac injury in a mouse model mimicking thrombotic thrombocytopenic purpura
Le Besnerais, M., Favre, J., Denis, C. V., Mulder, P., Martinet, J., Nicol, L., Levesque, H., Veyradier, A., Kopić, A., Motto, D. G., Coppo, P., Richard, V., Benhamou, Y.
Published in Journal of thrombosis and haemostasis (01.10.2016)
Published in Journal of thrombosis and haemostasis (01.10.2016)
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Journal Article
Prognostic value of inhibitory anti‐ADAMTS13 antibodies in adult‐acquired thrombotic thrombocytopenic purpura
Coppo, P., Wolf, M., Veyradier, A., Bussel, A., Malot, S., Millot, G. A., Daubin, C., Bordessoule, D., Pène, F., Mira, J. P., Heshmati, F., Maury, E., Guidet, B., Boulanger, E., Galicier, L., Parquet, N., Vernant, J. P., Rondeau, E., Azoulay, E., Schlemmer, B.
Published in British journal of haematology (01.01.2006)
Published in British journal of haematology (01.01.2006)
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Validation of the first commercial ELISA for type 2N von Willebrand's disease diagnosis
VEYRADIER, A., CARON, C., TERNISIEN, C., WOLF, M., TROSSAERT, M., FRESSINAUD, E., GOUDEMAND, J.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.11.2011)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.11.2011)
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Telemedicine in thrombotic microangiopathies: A way forward in rare diseases requiring emergency care
Coppo, P, Corre, E, Rondeau, E, Benhamou, Y, Bachet, A, Stépanian, A, Veyradier, A
Published in La revue de medecine interne (01.08.2016)
Published in La revue de medecine interne (01.08.2016)
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Journal Article
The revolution of monoclonal antibodies in the treatment of thrombotic microangiopathy
Sauvètre, G, Grange, S, Froissart, A, Veyradier, A, Coppo, P, Benhamou, Y
Published in La revue de medecine interne (01.05.2015)
Published in La revue de medecine interne (01.05.2015)
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Journal Article
Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)
Veyradier, A., Lavergne, J‐M., Ribba, A‐S., Obert, B., Loirat, C., Meyer, D., Girma, J‐P.
Published in Journal of thrombosis and haemostasis (01.03.2004)
Published in Journal of thrombosis and haemostasis (01.03.2004)
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Thrombotic thrombocytopenic purpura in a newborn
Ghariani, I, Jmili-Braham, N, Azzebi, O, Kortas, M, Veyradier, A, Bakir, L
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.01.2016)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.01.2016)
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Journal Article
Human Immunodeficiency Virus‐Associated Thrombotic Microangiopathies: Clinical Characteristics and Outcome According to ADAMTS13 Activity
Malak, S., Wolf, M., Millot, G. A., Mariotte, E., Veyradier, A., Meynard, J.‐L., Korach, J.‐M., Malot, S., Bussel, A., Azoulay, E., Boulanger, E., Galicier, L., Devaux, E., Eschwège, V., Gallien, S., Adrie, C., Schlemmer, B., Rondeau, E., Coppo, P.
Published in Scandinavian journal of immunology (01.09.2008)
Published in Scandinavian journal of immunology (01.09.2008)
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Compound heterozygosity or heterozygosity with two mutations in cis on the same allele? A rebuttal to the letter to the Editors: Koessler et al. Von Willebrand disease caused by compound heterozygosity for p.R854Q and p.R760C: diagnostic and therapeutic implications. Haemophilia 2011; 17: e240-2
Veyradier, A, Fressinaud, E, Goudemand, J
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.09.2011)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.09.2011)
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