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1. Randomized Trial of COBRA PzF Stenting to Reduce the Duration of Triple Therapy: The COBRA-REDUCE Trial

2. Prevalence and location of coronary artery disease in anomalous aortic origin of coronary arteries

3. Quantitative flow ratio versus fractional flow reserve for coronary revascularisation guidance (FAVOR III Europe): a multicentre, randomised, non-inferiority trial

5. Erratum to “One year results of Coronary bifurcation revascularization with the re-POT provisional sequential technique. The CABRIOLET registry” [Int J Cardiol. 2024 Feb 15;397:131632.]

12. 2-Year Clinical Outcomes of an Abluminal Groove–Filled Biodegradable-Polymer Sirolimus-Eluting Stent Compared With a Durable-Polymer Everolimus-Eluting Stent

14. TCT-185 Safety and Performance Registry for an All-Comers Subject Population With the Limus-Eluting Orsiro Mission Stent System Within Daily Clinical Practice: 12-Month Results of the BIOFLOW-VIII Registry

18. 6- Versus 24-Month Dual Antiplatelet Therapy After Implantation of Drug-Eluting Stents in Patients Nonresistant to Aspirin: Final Results of the ITALIC Trial (Is There a Life for DES After Discontinuation of Clopidogrel)

19. 9-Month Clinical and Angiographic Outcomes of the COBRA Polyzene-F NanoCoated Coronary Stent System

20. The POT-PUFF sign: an angiographic mark of stent malapposition during proximal optimisation

22. 6- Versus 24-Month Dual Antiplatelet Therapy After Implantation of Drug-Eluting Stents in Patients Nonresistant to Aspirin: The Randomized, Multicenter ITALIC Trial

23. Five-year clinical outcomes using the bioresorbable vascular scaffold: Insights from the FRANCE ABSORB registry

27. Ticagrelor Monotherapy or Dual Antiplatelet Therapy After Drug‐Eluting Stent Implantation: Per‐Protocol Analysis of the GLOBAL LEADERS Trial

28. High On-Treatment Platelet Reactivity After Prasugrel Loading Dose and Cardiovascular Events After Percutaneous Coronary Intervention in Acute Coronary Syndromes

29. Design and Rationale of a Randomized Trial of COBRA PzF Stenting to REDUCE Duration of Triple Therapy (COBRA-REDUCE)

30. Future culprit detection based on angiography-derived FFR

31. TCT-489 Three-Year Outcomes of Patients Treated With the Firehawk Stent Versus XIENCE Stent on the Basis of Diabetes Status: Subgroup Analysis of the TARGET All Comers Trial

33. Benefit and Risks of Aspirin in Addition to Ticagrelor in Acute Coronary Syndromes: A Post Hoc Analysis of the Randomized GLOBAL LEADERS Trial

34. Relation of Body Mass Index to High On-Treatment Platelet Reactivity and of Failed Clopidogrel Dose Adjustment According to Platelet Reactivity Monitoring in Patients Undergoing Percutaneous Coronary Intervention

35. Polymer ‐free Biolimus‐A9 coated thin strut stents for patients at high bleeding risk 1‐year results from the LEADERS FREE III study

36. Future culprit detection based on angiography‐derived FFR

37. Association of sex with outcomes in patients undergoing percutaneous coronary intervention: a subgroup analysis of the global leaders randomized clinical trial

38. Validation of the all-comers design:Results of the TARGET-AC substudy

39. Combined Abciximab REteplase Stent Study in Acute Myocardial Infarction (CARESS in AMI)

41. Platelet glycoprotein IIb/IIIa inhibition with coronary stenting for acute myocardial infarction

42. Ticagrelor versus clopidogrel in elective percutaneous coronary intervention (ALPHEUS): a randomised, open-label, phase 3b trial

43. Evaluation of the safety and efficacy of the Cobra PzF NanoCoated coronary stent in routine, consecutive, prospective, and high‐risk patients: The e‐Cobra study

44. Validation of the all-comers design: Results of the TARGET-AC substudy

45. Association of Sex With Outcomes in Patients Undergoing Percutaneous Coronary Intervention

48. Anticoagulant (Fluindione)-Aspirin Combination in Patients with High-Risk Atrial Fibrillation: A Randomized Trial (Fluindione, Fibrillation Auriculaire, Aspirin et Contraste Spontané; FFAACS)

50. Prospective evaluation of drug eluting self‐apposing stent for the treatment of unprotected left main coronary artery disease: 1‐year results of the TRUNC study

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