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201. Correction.

来源: Circulation. 2015年132卷19期e233页
In the article by Burke et al, "Current Science on Consumer Use of Mobile Health for Cardiovascular Disease Prevention: A Scientific Statement From the American Heart Association," which published ahead of print August 13, 2015, and appeared in the September 22, 2015, issue of the journal (Circulation. 2015;132:1157-1213. DOI: 10.1161/CIR.0000000000000232), several corrections were needed.1. On page 1203, in the first column, last paragraph, the second sentence read, "Because medication may be a component of the treatment, we also searched for meditation adherence." It has been changed to read, "Because medication may be a component of the treatment, we also searched for medication adherence." 2. On page 1204, in the second column, third complete paragraph, the second sentence read, "As with any other product that claims to improve health, groups will want to answers to certain questions…." It has been changed to read, "As with any other product that claims to improve health, groups will want answers to certain questions…."3. On page 1204, in the second column, last paragraph, the fourth sentence read, "However, the responsibility for generating evidence should not fall solely only on the product developers." It has been changed to read, "However, the responsibility for generating evidence should not fall solely on the product developers." These corrections have been made to the print version and to the current online version of the article, which is available at http://circ.ahajournals.org/content/132/12/1157.full

202. Response to Letter Regarding Article, "Systematic Review of Patients Presenting With Suspected Myocardial Infarction and Nonobstructive Coronary Arteries".

作者: Sivabaskari Pasupathy.;Tracy Air.;Rachel P Dreyer.;Rosanna Tavella.;John F Beltrame.
来源: Circulation. 2015年132卷19期e232页

203. Letter by Mahajan et al Regarding Article, "Systematic Review of Patients Presenting With Suspected Myocardial Infarction and Nonobstructive Coronary Arteries".

作者: Asha M Mahajan.;Kaitlyn E Dugan.;Harmony R Reynolds.
来源: Circulation. 2015年132卷19期e231页

204. Response to Letter Regarding Article, "Left Atrial Appendage Occlusion Debate Revisited".

作者: Richard P Whitlock.;Jeff S Healey.;David R Holmes.
来源: Circulation. 2015年132卷19期e230页

205. Letter by Salzberg and Emmert Regarding Article, "Left Atrial Appendage Occlusion Debate Revisited".

作者: Sacha P Salzberg.;Maximilian Y Emmert.
来源: Circulation. 2015年132卷19期e229页

206. Neonatal Management of a Giant Right Atrial Appendage Aneurysm.

作者: Robert D Tunks.;Jozef Malysz.;Joseph B Clark.
来源: Circulation. 2015年132卷19期e226-8页

207. Extensive Intramural Esophageal Hematoma After Transesophageal Echocardiography During Atrial Fibrillation Ablation.

作者: Min-young Kim.;Fu Siong Ng.;Ben Ariff.;George B Hanna.;Zachary Whinnett.;Prapa Kanagaratnam.;Mark Tanner.;Phang Boon Lim.
来源: Circulation. 2015年132卷19期1847-9页

208. ECG Response: November 10, 2015.

作者: Philip J Podrid.
来源: Circulation. 2015年132卷19期1846页

209. Myocardial Protection During Cardiotoxic Chemotherapy.

作者: Ronald M Witteles.;Xavier Bosch.
来源: Circulation. 2015年132卷19期1835-45页

210. Introduction to the Cardio-Oncology Miniseries.

作者: Ravin Davidoff.;Michael Fifer.;Sanjeev Francis.
来源: Circulation. 2015年132卷19期1834页

211. Catheter-based therapies for patients with medication-refractory pulmonary arterial hypertension.

作者: Jane A Leopold.
来源: Circ Cardiovasc Interv. 2015年8卷11期e003332页

212. Restoring platelet function in patients on P2Y12 receptor inhibitor treatment: still some issues to be solved!

作者: Dirk Sibbing.;Steffen Massberg.
来源: Circ Cardiovasc Interv. 2015年8卷11期e003257页

213. First reported case of transcatheter mitral valve implantation in mitral annular calcification with a fully repositionable and self-expanding valve.

作者: Zhan Yun Lim.;Ricardo Boix.;Bernard Prendergast.;Ronak Rajani.;Simon Redwood.;Jane Hancock.;Christopher Young.;Vinayak Vinnie Bapat.
来源: Circ Cardiovasc Interv. 2015年8卷11期e003031页

214. Hemodynamic, functional, and clinical responses to pulmonary artery denervation in patients with pulmonary arterial hypertension of different causes: phase II results from the Pulmonary Artery Denervation-1 study.

作者: Shao-Liang Chen.;Hang Zhang.;Du-Jiang Xie.;Juan Zhang.;Ling Zhou.;Alexander M K Rothman.;Gregg W Stone.
来源: Circ Cardiovasc Interv. 2015年8卷11期e002837页
The mechanisms underlying pulmonary arterial hypertension (PAH) are multifactorial. The efficacy of pulmonary artery denervation (PADN) for idiopathic PAH treatment has been evaluated. This study aimed to analyze the hemodynamic, functional, and clinical responses to PADN in patients with PAH of different causes.

215. Efficacy of ex vivo autologous and in vivo platelet transfusion in the reversal of P2Y12 inhibition by clopidogrel, prasugrel, and ticagrelor: the APTITUDE study.

作者: Stephen A O'Connor.;Julien Amour.;Anne Mercadier.;Réjane Martin.;Mathieu Kerneis.;Jérémie Abtan.;Delphine Brugier.;Johanne Silvain.;Olivier Barthélémy.;Pascal Leprince.;Gilles Montalescot.;Jean-Philippe Collet.; .
来源: Circ Cardiovasc Interv. 2015年8卷11期e002786页
Allogenic platelet transfusions (PT) are administered to treat excessive bleeding in patients on P2Y12 receptor inhibitors (RI). We assessed the effect of ex vivo and in vivo PT on platelet activation and aggregation in patients on dual antiplatelet therapy.

216. Pulmonary artery denervation reduces pulmonary artery pressure and induces histological changes in an acute porcine model of pulmonary hypertension.

作者: Alexander M K Rothman.;Nadine D Arnold.;William Chang.;Oliver Watson.;Andrew J Swift.;Robin Condliffe.;Charlie A Elliot.;David G Kiely.;S Kim Suvarna.;Julian Gunn.;Allan Lawrie.
来源: Circ Cardiovasc Interv. 2015年8卷11期e002569页
Pulmonary arterial hypertension is a devastating disease with high morbidity and mortality and limited treatment options. Recent studies have shown that pulmonary artery denervation improves pulmonary hemodynamics in an experimental model and in an early clinical trial. We aimed to evaluate the nerve distribution around the pulmonary artery, to determine the effect of radiofrequency pulmonary artery denervation on acute pulmonary hypertension induced by vasoconstriction, and to demonstrate denervation of the pulmonary artery at a histological level.

217. Green Tea Catechin Normalizes the Enhanced Ca2+ Sensitivity of Myofilaments Regulated by a Hypertrophic Cardiomyopathy-Associated Mutation in Human Cardiac Troponin I (K206I).

作者: Chad M Warren.;Chehade N Karam.;Beata M Wolska.;Tomoyoshi Kobayashi.;Pieter P de Tombe.;Grace M Arteaga.;J Martijn Bos.;Michael J Ackerman.;R John Solaro.
来源: Circ Cardiovasc Genet. 2015年8卷6期765-73页
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease characterized by thickening of ventricular walls and decreased left ventricular chamber volume. The majority of HCM-associated mutations are found in genes encoding sarcomere proteins. Herein, we set out to functionally characterize a novel HCM-associated mutation (K206I-TNNI3) and elucidate the mechanism of dysfunction at the level of myofilament proteins.

218. Calcium Signaling Pathway Genes RUNX2 and CACNA1C Are Associated With Calcific Aortic Valve Disease.

作者: Sandra Guauque-Olarte.;David Messika-Zeitoun.;Arnaud Droit.;Maxime Lamontagne.;Joël Tremblay-Marchand.;Emilie Lavoie-Charland.;Nathalie Gaudreault.;Benoit J Arsenault.;Marie-Pierre Dubé.;Jean-Claude Tardif.;Simon C Body.;Jonathan G Seidman.;Catherine Boileau.;Patrick Mathieu.;Philippe Pibarot.;Yohan Bossé.
来源: Circ Cardiovasc Genet. 2015年8卷6期812-22页
Calcific aortic valve stenosis (AS) is a life-threatening disease with no medical therapy. The genetic architecture of AS remains elusive. This study combines genome-wide association studies, gene expression, and expression quantitative trait loci mapping in human valve tissues to identify susceptibility genes of AS.

219. Cardiac Disease Status Dictates Functional mRNA Targeting Profiles of Individual MicroRNAs.

作者: Scot J Matkovich.;Gerald W Dorn.;Tiffani C Grossenheider.;Peter A Hecker.
来源: Circ Cardiovasc Genet. 2015年8卷6期774-84页
MicroRNAs are key players in cardiac stress responses, but the mRNAs, whose abundance and translational potential are primarily affected by changes in cardiac microRNAs, are not well defined. Stimulus-induced, large-scale alterations in the cardiac transcriptome, together with consideration of the law of mass action, further suggest that the mRNAs most substantively targeted by individual microRNAs will vary between unstressed and stressed conditions. To test the hypothesis that microRNA target profiles differ in health and disease, we traced the fate of empirically determined miR-133a and miR-378 targets in mouse hearts undergoing pressure overload hypertrophy.

220. Efficacy of various percutaneous interventions for in-stent restenosis: comprehensive network meta-analysis of randomized controlled trials.

作者: Ankur Sethi.;Gurveen Malhotra.;Sukhchain Singh.;Param P Singh.;Sandeep Khosla.
来源: Circ Cardiovasc Interv. 2015年8卷11期e002778页
In-stent restenosis (ISR) remains a difficult problem in interventional cardiology. The relative efficacy and safety of available interventions is not clear. We aimed to perform a network meta-analysis using both direct evidence and indirect evidence to compare all available interventions.
共有 46145 条符合本次的查询结果, 用时 2.7515304 秒