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Paul COPPO
Paul COPPO
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Verified email at aphp.fr
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Cited by
Cited by
Year
Development and validation of the HScore, a score for the diagnosis of reactive hemophagocytic syndrome
L Fardet, L Galicier, O Lambotte, C Marzac, C Aumont, D Chahwan, ...
Arthritis & rheumatology 66 (9), 2613-2620, 2014
11462014
Caplacizumab treatment for acquired thrombotic thrombocytopenic purpura
M Scully, SR Cataland, F Peyvandi, P Coppo, P Knöbl, ...
New England Journal of Medicine 380 (4), 335-346, 2019
7502019
Thrombotic thrombocytopenic purpura
BS Joly, P Coppo, A Veyradier
Blood, The Journal of the American Society of Hematology 129 (21), 2836-2846, 2017
6322017
Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases
MA Dragon-Durey, V Fremeaux-Bacchi, C Loirat, J Blouin, P Niaudet, ...
Journal of the American Society of Nephrology 15 (3), 787-795, 2004
4352004
Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies
M Scully, S Cataland, P Coppo, J De La Rubia, KD Friedman, JK Hovinga, ...
Journal of thrombosis and haemostasis 15 (2), 312-322, 2017
4162017
Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic microangiopathies: the French TMA reference center experience
P Coppo, M Schwarzinger, M Buffet, A Wynckel, K Clabault, C Presne, ...
PloS one 5 (4), e10208, 2010
3782010
Reactive hemophagocytic syndrome in adults: a retrospective analysis of 162 patients
S Rivière, L Galicier, P Coppo, C Marzac, C Aumont, O Lambotte, L Fardet
The American journal of medicine 127 (11), 1118-1125, 2014
3572014
Gene expression profiling identifies emerging oncogenic pathways operating in extranodal NK/T-cell lymphoma, nasal type
Y Huang, A De Reyniès, L De Leval, B Ghazi, N Martin-Garcia, M Travert, ...
Blood, The Journal of the American Society of Hematology 115 (6), 1226-1237, 2010
3432010
Thrombotic thrombocytopenic purpura
JA Kremer Hovinga, P Coppo, B Lämmle, JL Moake, T Miyata, ...
Nature reviews Disease primers 3 (1), 1-17, 2017
3332017
Epidemiology and pathophysiology of adulthood-onset thrombotic microangiopathy with severe ADAMTS13 deficiency (thrombotic thrombocytopenic purpura): a cross-sectional analysis …
E Mariotte, E Azoulay, L Galicier, E Rondeau, F Zouiti, P Boisseau, ...
The Lancet Haematology 3 (5), e237-e245, 2016
3092016
Prognostic value of anti-ADAMTS13 antibody features (Ig isotype, titer, and inhibitory effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic …
S Ferrari, F Scheiflinger, M Rieger, G Mudde, M Wolf, P Coppo, JP Girma, ...
Blood 109 (7), 2815-2822, 2007
2992007
Efficacy and safety of first-line rituximab in severe, acquired thrombotic thrombocytopenic purpura with a suboptimal response to plasma exchange. Experience of the French …
A Froissart, M Buffet, A Veyradier, P Poullin, F Provôt, S Malot, ...
Critical care medicine 40 (1), 104-111, 2012
2842012
Unexpected frequency of Upshaw-Schulman syndrome in pregnancy-onset thrombotic thrombocytopenic purpura
M Moatti-Cohen, C Garrec, M Wolf, P Boisseau, L Galicier, E Azoulay, ...
Blood, The Journal of the American Society of Hematology 119 (24), 5888-5897, 2012
2752012
ISTH guidelines for treatment of thrombotic thrombocytopenic purpura
XL Zheng, SK Vesely, SR Cataland, P Coppo, B Geldziler, A Iorio, ...
Journal of Thrombosis and Haemostasis 18 (10), 2496-2502, 2020
2642020
Prognostic factors of early death in a cohort of 162 adult haemophagocytic syndrome: impact of triggering disease and early treatment with etoposide
M Arca, L Fardet, L Galicier, S Rivière, C Marzac, C Aumont, O Lambotte, ...
British journal of haematology 168 (1), 63-68, 2015
2042015
ISTH guidelines for the diagnosis of thrombotic thrombocytopenic purpura
XL Zheng, SK Vesely, SR Cataland, P Coppo, B Geldziler, A Iorio, ...
Journal of Thrombosis and Haemostasis 18 (10), 2486-2495, 2020
2032020
Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet …
P Coppo, D Bengoufa, A Veyradier, M Wolf, A Bussel, GA Millot, S Malot, ...
Medicine 83 (4), 233-244, 2004
1882004
Preemptive rituximab infusions after remission efficiently prevent relapses in acquired thrombotic thrombocytopenic purpura
M Hie, J Gay, L Galicier, F Provôt, C Presne, P Poullin, G Bonmarchand, ...
Blood, The Journal of the American Society of Hematology 124 (2), 204-210, 2014
1672014
JAK3 deregulation by activating mutations confers invasive growth advantage in extranodal nasal-type natural killer cell lymphoma
A Bouchekioua, L Scourzic, O De Wever, Y Zhang, P Cervera, ...
Leukemia 28 (2), 338-348, 2014
1662014
High-dose plasma infusion versus plasma exchange as early treatment of thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome
P Coppo, A Bussel, S Charrier, C Adrie, L Galicier, E Boulanger, ...
Medicine 82 (1), 27-38, 2003
1612003
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