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52. Neointimal hyperplasia of ultra-thin stents with microcrystalline sirolimus or durable polymer everolimus-eluting stents: 6- and 24-month results of the DESSOLVE III OCT study

53. Preclinical evaluation of a thin-strut bioresorbable scaffold (ArterioSorb): acute-phase invasive imaging assessment and hemodynamic implication.

54. Vulnerable plaques and patients: state-of-the-art

56. Angiographic and clinical outcomes of STEMI patients treated with bioresorbable or metallic everolimus-eluting stents: a pooled analysis of individual patient data

57. Clinical outcomes of bioabsorbable polymer sirolimus-eluting stents versus durable polymer everolimus-eluting stents: two-year follow-up of the DESSOLVE III trial

58. The influence of implantation techniques on lesion oriented-outcomes in Absorb BVS and Xience EES lesions treated in routine clinical practice at complete three year follow-up: AIDA trial QCA substudy

60. Post-implantation shear stress assessment: an emerging tool for differentiation of bioresorbable scaffolds

61. Site vs. core laboratory variability in computed tomographic angiography-derived SYNTAX scores in the SYNTAX III trial.

62. The Long-Term Impact of Post-Procedural Asymmetry and Eccentricity of Bioresorbable Everolimus-Eluting Scaffold and Metallic Everolimus-Eluting Stent on Clinical Outcomes in the ABSORB II Trial

63. Site versus Core Laboratory SYNTAX score variability

66. TCT-170 Endothelial Shear Stress and Vascular Remodeling in Bioresorbable Scaffold and Metallic Stent

67. TCT-186 Preclinical Evaluation of a Novel Thin-Strut PLLA Bioresorbable Scaffold in Porcine Coronary Artery at 6-Month Follow-Up

68. TCT-179 The Influence of Increasing Stent Length on Outcomes in Absorb BVS or Xience EES-Treated Patients in Routine Clinical PCI Practice: AIDA Trial Substudy

69. TCT-111 Clinical Implication of Quantitative Flow Ratio After Percutaneous Coronary Intervention for Three Vessel Disease

71. Expert recommendations on the assessment of wall shear stress in human coronary arteries: existing methodologies, technical considerations, and clinical applications

72. Acute and long-term relocation of minimal lumen area after bioresorbable scaffold or metallic stent implantation

73. Validation of the updated logistic clinical SYNTAX score for all-cause mortality in the GLOBAL LEADERS trial

74. Predictive ability of ACEF and ACEF II score in patients undergoing percutaneous coronary intervention in the GLOBAL LEADERS study

75. A prospective multicentre randomised all-comers trial to assess the safety and effectiveness of the thin-strut sirolimus-eluting coronary stent SUPRAFLEX: rationale and design of the Thin Strut Sirolimus-eluting Stent in All Comers Population vs Everolimus-eluting Stent (TALENT) trial

76. Early strut protrusion and late neointima thickness in the Absorb bioresorbable scaffold: a serial wall shear stress analysis up to five years

78. The impact of plaque type on strut embedment/protrusion and shear stress distribution in bioresorbable scaffold

79. Clinical outcomes of state-of-the-art percutaneous coronary revascularisation in patients with three-vessel disease: two-year follow-up of the SYNTAX II study

80. How does the failure of Absorb apply to the other bioresorbable scaffolds? An expert review of first-in-man and pivotal trials

83. Feasibility of planning coronary artery bypass grafting based only on coronary computed tomography angiography and CT-derived fractional flow reserve: a pilot survey of the surgeons involved in the randomized SYNTAX III Revolution trial

84. LONG-TERM SAFETY OF TICAGRELOR MONOTHERAPY IN PATIENTS UNDERGOING PCI FOR STABLE CORONARY ARTERY DISEASE IN THE GLOBAL LEADERS STUDY: IMPACT OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE

85. LONG-TERM TICAGRELOR MONOTHERAPY IN ELDERLY PATIENTS UNDERGOING PCI IN THE GLOBAL LEADERS STUDY

86. PREDICTIVE ABILITY OF THE PARIS RISK SCORE IN ALL-COMERS PATIENTS UNDERGOING PCI WITH DRUG ELUTING STENTS: EXTERNAL VALIDATION IN THE GLOBAL LEADERS STUDY

87. CORE LABORATORY ASSESSMENT OF NON-FATAL Q-WAVE MYOCARDIAL INFARCTION IN THE GLOBAL LEADERS TRIAL: METHODS AND FINDINGS

88. Serial Optical Coherence Tomography at Baseline, 7 Days, and 1, 3, 6 and 12 Months After Bioresorbable Scaffold Implantation in a Growing Porcine Model

89. Mechanical properties and performances of contemporary drug-eluting stent: focus on the metallic backbone

90. Joint consensus on the use of OCT in coronary bifurcation lesions by the European and Japanese bifurcation clubs

91. Impact of post‐procedural minimal stent area on 2‐year clinical outcomes in the SYNTAX II trial

92. A randomised comparison of healing response between the BuMA Supreme stent and the XIENCE stent at one-month and two-month follow-up: PIONEER-II OCT randomised controlled trial

93. Three-year follow-up of the randomised comparison between an everolimus-eluting bioresorbable scaffold and a durable polymer everolimus-eluting metallic stent in patients with ST-segment elevation myocardial infarction (TROFI II trial)

94. The impact of plaque type on strut embedment/protrusion and shear stress distribution in bioresorbable scaffold.

95. Post-implantation shear stress assessment: an emerging tool for differentiation of bioresorbable scaffolds

96. Coronary computed tomography angiography for heart team decision-making in multivessel coronary artery disease

97. Relation between bioresorbable scaffold sizing using QCA-Dmax and long-term clinical outcomes in 1,232 patients from three study cohorts (ABSORB Cohort B, ABSORB EXTEND, and ABSORB II)

98. TCT-112 Patient-oriented clinical outcomes and net adverse cardiovascular event in the Global Leaders trial

99. TCT-430 In vitro and preclinical evaluation of a thin-strut bioresorbable scaffold: results from bench testing and acute phase study in a non-atherosclerotic porcine model.

100. TCT-673 Two years clinical outcomes with the state-of-the-art PCI for the treatment of bifurcation lesions: A Sub-analysis of the SYNTAX II study

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