Zobrazeno 1 - 10 of 28 pro vyhledávání: '"MESH : Thrombocytopenia"'
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Fcγ receptor expression on splenic macrophages in adult immune thrombocytopenia
Autor: Bernard Bonnotte, Annemieke G. Laarhoven, Kim Santegoets, Philippe Saas, Maxime Samson, Gestur Vidarsson, Sylvain Audia, Olivier Facy, Timothy R D J Radstake, Pablo Ortega-Deballon, Nona Janikashvili
Publikováno v: Clinical and Experimental Immunology
Clinical and Experimental Immunology, Wiley, 2017, 188 (2), pp.275-282. ⟨10.1111/cei.12935⟩
Clinical and Experimental Immunology, 188, 275-282
Clinical and Experimental Immunology, 188(2), 275. Wiley-Blackwell
Clinical and Experimental Immunology, 188, 2, pp. 275-282
Clinical and experimental immunology, 188(2), 275-282. Wiley-Blackwell
Clinical and Experimental Immunology, Wiley, 2017, 188 (2), pp.275-282. 〈http://onlinelibrary.wiley.com/doi/10.1111/cei.12935/abstract;jsessionid=FBA5B398503A03620104AAB3C880D684.f02t03?systemMessage=Wiley+Online+Library+%27Journal+Subscribe+%2F+Renew%27+page+will+be+down+on+Wednesday+05th+July+starting+at+08.00+EDT+%2F+13.00+BST+%2F+17.30+IST+for+up+to+75+minutes+due+to+essential+maintenance.〉. 〈10.1111/cei.12935〉
Summary Splenic macrophages play a key role in immune thrombocytopenia (ITP) pathogenesis by clearing opsonized platelets. Fcγ receptors (FcγR) participate in this phenomenon, but their expression on splenic macrophages and their modulation by trea
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdcb58ff87b7880a8fbd365c5a5237a6
https://hal-univ-bourgogne.archives-ouvertes.fr/hal-01556448
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3
Fièvre hémorragique à syndrome rénal associée à l’hantavirus Séoul en France : une observation
Autor: J.-F. Dufour, Jean-Marc Reynes, A. Bour, X. Plaisancie
Publikováno v: La Revue De Médecine Interne
La Revue De Médecine Interne, Elsevier, 2016, 37 (7), pp.493-496. ⟨10.1016/j.revmed.2015.10.343⟩
La Revue de Médecine Interne
La Revue de Médecine Interne, 2016, 37 (7), pp.493-496. ⟨10.1016/j.revmed.2015.10.343⟩
International audience; Introduction. – Rodents are hantavirus hosts. In Europe, hantaviruses are responsible for human infectionsresulting in hemorrhagic fever with renal syndrome. Thousands of Puumala virus infections are reportedannually in Euro
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bc4e3ed82371f92508daf1e9c08d5a2
https://doi.org/10.1016/j.revmed.2015.10.343
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4
The Addition of Bevacizumab to Oxaliplatin-Based Chemotherapy: Impact Upon Hepatic Sinusoidal Injury and Thrombocytopenia
Autor: J.N. Vauthey, Binsah George, Kanwal Pratap Singh Raghav, Evelyn Loyer, Michael J. Overman, Scott Kopetz, Leonard B. Saltz, Paulo M. Hoff, Thibault Mazard, Brian P. Hobbs, Wei Qiao, Renata Ferrarotto, Karime Kalil Machado
Publikováno v: JNCI: Journal of the National Cancer Institute
JNCI: Journal of the National Cancer Institute, Oxford University Press (OUP), 2018, 110 (8), pp.888-894. ⟨10.1093/jnci/djx288⟩
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
International audience; Background:Oxaliplatin-based chemotherapy can cause hepatic sinusoidal injury (HSI), portal hypertension, and splenic sequestration of platelets. Evidence suggests that bevacizumab may protect against HSI.Methods:Two cohorts o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::220ec46c617e3dc7d6fd4b60d3101131
https://hal.umontpellier.fr/hal-02291196
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5
Évaluation de la prise en charge de l’analgésie postopératoire en chirurgie de reconstruction du pavillon auriculaire selon Nagata (premier temps avec prélèvement autologue de cartilage costal) : analyse rétrospective des résultats avec cathéter d´infiltration cicatricielle versus cathéter paravertébral
Autor: wojciek, benjamin
Publikováno v: Médecine humaine et pathologie. 2017
Introduction: microtia is an abnormality of development of the external ear that can be isolated or integrated into a polymalformative syndrome. Auricular reconstruction surgery is possible and the main technique is the one described by Nagata, the f
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2592::25873b4a86ed1d326eb5ade4c094e0de
https://dumas.ccsd.cnrs.fr/dumas-01730588
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7
Mechanisms and etiologies of thrombocytopenia in the intensive care unit: impact of extensive investigations
Autor: Robin Noel, Emmanuel Demaistre, Hervé Devilliers, Nadiejda Antier, Jean-Marc Doise, Jean-Pierre Quenot
Publikováno v: Annals of Intensive Care
Annals of Intensive Care, BioMed Central, 2014, 4 (1), pp.24. 〈10.1186/s13613-014-0024-x〉
Annals of Intensive Care, SpringerOpen, 2014, 4 (1), pp.24. ⟨10.1186/s13613-014-0024-x⟩
Background Thrombocytopenia is common in the intensive care unit. Potential mechanisms and etiologies behind this phenomenon are multiple and often entangled. We assessed the effect of a systematic approach, using routinely available tests, on the pr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4012d208bf283c8e9c963de7fc34b58c
https://doi.org/10.1186/s13613-014-0024-x
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8
LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2B
Autor: Valérie Proulle, Audrey Pietrzyk-Nivau, Frédéric Adam, Sonia Poirault-Chassac, Cécile V. Denis, Christelle Soukaseum, Peter J. Lenting, Jean-Philippe Rosa, Jean-Claude Bordet, Vincent Muczynski, Gabriel Aymé, Chantal Rothschild, Dominique Baruch, Eliane Berrou, Marijke Bryckaert, Olivier D. Christophe, Caterina Casari, Alexandre Kauskot
Publikováno v: JCI Insight
JCI Insight, American Society for Clinical Investigation, 2016, 1 (16), pp.e88643. ⟨10.1172/jci.insight.88643⟩
International audience; von Willebrand disease type 2B (VWD-type 2B) is characterized by gain-of-function mutations of von Willebrand factor (vWF) that enhance its binding to platelet glycoprotein Ibα and alter the protein's multimeric structure. Pa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::402474e3982b906b1890052998992abb
https://hal-pasteur.archives-ouvertes.fr/pasteur-03209475
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9
[Diagnosis of inherited thrombocytopenia]
Autor: Baccini, V, Alessi, Marie-Christine
Publikováno v: La Revue De Médecine Interne
La Revue De Médecine Interne, Elsevier, 2016, 37 (2), pp.117-26
La Revue de Médecine Interne
La Revue de Médecine Interne, Elsevier, 2016, 37 (2), pp.117-26
International audience; Inherited thrombocytopenias are rare, heterogenous and probably under-diagnosed because often classified as autoimmune thrombocytopenia. About 20 genes were described responsible for these thrombocytopenias. Precise diagnosis
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0e8ab902d6d8bbbc20dea91c4521e80e
https://hal.archives-ouvertes.fr/hal-01478134
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10
Argatroban in the management of heparin-induced thrombocytopenia: a multicenter clinical trial
Autor: Sandrine Grosjean, Brigitte Tardy-Poncet, Christine Biron-Andreani, Emmanuel de Maistre, Yves Gruel, Alain Wynckel, Jérôme Morel, Philippe Nguyen, Lelia Grunebaum, Jean-Claude Thiranos, Pierre-Emmanuel Morange, Judith Villacorta-Torres
Publikováno v: Critical Care
Critical Care, BioMed Central, 2015, 19, pp.396. ⟨10.1186/s13054-015-1109-0⟩
Critical Care, 2015, 19, pp.396. ⟨10.1186/s13054-015-1109-0⟩
Introduction The aim of this study was to collect data in France in patients with heparin-induced thrombocytopenia who required parenteral anticoagulation and for whom other non-heparin anticoagulant therapies were contraindicated including patients
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d3fb4a4196d29fab7cfe5ed24f22933
https://doi.org/10.1186/s13054-015-1109-0
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