P
Paul Coppo
Researcher at University of Paris
Publications - 245
Citations - 9732
Paul Coppo is an academic researcher from University of Paris. The author has contributed to research in topics: Thrombotic thrombocytopenic purpura & Thrombotic microangiopathy. The author has an hindex of 43, co-authored 210 publications receiving 7274 citations. Previous affiliations of Paul Coppo include French Institute of Health and Medical Research & Pierre-and-Marie-Curie University.
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Journal ArticleDOI
Development and validation of the HScore, a score for the diagnosis of reactive hemophagocytic syndrome.
Laurence Fardet,Lionel Galicier,Olivier Lambotte,Christophe Marzac,Cedric Aumont,Doumit Chahwan,Paul Coppo,Gilles Hejblum +7 more
TL;DR: Because it has no unique clinical, biologic, or histologic features, reactive hemophagocytic syndrome may be difficult to distinguish from other diseases such as severe sepsis or hematologic malignancies.
Journal ArticleDOI
Caplacizumab Treatment for Acquired Thrombotic Thrombocytopenic Purpura.
Marie Scully,Spero R. Cataland,Flora Peyvandi,Paul Coppo,Paul Knöbl,Johanna A. Kremer Hovinga,Ara Metjian,Javier de la Rubia,Katerina Pavenski,Filip Callewaert,Debjit Biswas,Hilde De Winter,R.K. Zeldin,Hercules Investigators +13 more
TL;DR: In this paper, a double-blind, controlled trial was conducted to evaluate the effect of caplacizumab on platelet normalization and recurrence of TTP.
Journal ArticleDOI
Thrombotic thrombocytopenic purpura.
TL;DR: Long-term follow-up of patients with TTP is crucial to identify the occurrence of other autoimmune diseases, to control relapses, and to evaluate psychophysical sequelae.
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Heterozygous and Homozygous Factor H Deficiencies Associated with Hemolytic Uremic Syndrome or Membranoproliferative Glomerulonephritis: Report and Genetic Analysis of 16 Cases
Marie-Agnès Dragon-Durey,Véronique Frémeaux-Bacchi,Chantal Loirat,Jacques Blouin,Patrick Niaudet,Georges Deschênes,Paul Coppo,Wolf H. Fridman,Laurence Weiss +8 more
TL;DR: The variability in the clinical progression of kidney diseases associated with FH deficiencies is emphasized, and genetic analysis reveals the molecular abnormalities associated withFH deficiencies to be polymorphous.
Journal ArticleDOI
Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies.
Marie Scully,Spero R. Cataland,Paul Coppo,J de la Rubia,Kenneth D. Friedman,J. A. Kremer Hovinga,Bernhard Lämmle,Masanori Matsumoto,Katerina Pavenski,E Sadler,Ravi Sarode,Haiwa Wu +11 more
TL;DR: The consensus defines diagnosis, disease monitoring and response to treatment in thrombotic microangiopathies and TTP and requirements for ADAMTS‐13 are given.