维普中文期刊产品整合服务
59篇 您的检索式:作者名="Hebbar V"
    题名 作者 年代 出处 被引量
1Delineation of epicardial stenosis in patients with microvascular disease using pressure drop coefficient:A pilot outcome study显示文摘AIM To investigate the patient-outcomes of newly developed pressure drop coefficient(CDP) in diagnosing epicardial stenosis(ES) in the presence of concomitant microvascular disease(MVD).METHODS Patients from our clinical trial were divided into two subgroups with:(1) cut-off of coronary flow reserve(CFR) < 2.0;and(2) diabetes.First,correlations were performed for both subgroups between CDP and hyperemic microvascular resistance(HMR),a diagnostic parameter for assessing the severity of MVD.Linear regression analysis was used for these correlations.Further,in each of the subgroups,comparisons were made between fractional flow reserve(FFR) < 0.75 and CDP > 27.9 groups for assessing major adverse cardiac events(MACE:Primary outcome).Comparisons were also made between the survival curves for FFR < 0.75 and CDP > 27.9 groups.Two tailed chi-squared and Fischer's exact tests were performed for comparison of the primary outcomes,and the log-rank test was used to compare the Kaplan-Meier survival curves.P < 0.05 for all tests was considered statistically significant.RESULTS Significant linear correlations were observed between CDP and HMR for both CFR < 2.0(r = 0.58,P < 0.001) and diabetic(r = 0.61,P < 0.001) patients.In the CFR < 2.0 subgroup,the %MACE(primary outcomes) for CDP > 27.9 group(7.7%,2/26) was lower than FFR < 0.75 group(3/14,21.4%);P = 0.21.Similarly,in the diabetic subgroup,the %MACE for CDP > 27.9 group(12.5%,2/16) was lower than FFR < 0.75 group(18.2%,2/11);P = 0.69.Survival analysis for CFR < 2.0 subgroup indicated better event-free survival for CDP > 27.9 group(n = 26) when compared with FFR < 0.75 group(n = 14);P = 0.10.Similarly,for the diabetic subgroup,CDP > 27.9 group(n = 16) showed higher survival times compared to FFR group(n = 11);P = 0.58.CONCLUSION CDP correlated significantly with HMR and resulted in better %MACE as well as survival rates in comparison to FFR.These positive trends demonstrate that CDP could be a potential diagnostic endpoint for delineating MVD with or without ES.Ullhas Udaya Hebbar Mohamed A Effat Srikara V Peelukhana Imran Arif Rupak K Banerjee 2017World Journal of Cardiology2017,9,12:2
2Studies on NPK drip fertigation in field grown tomato (Lycopersicon esculentum Mill显示文摘Hebbar S S Ramachandrappa B K Nanjappa H V 2004European Journal of Agronomy2004,21,1:1
3Studies on NPK drip fertigation in field grown tomato显示文摘Hebbar S S Ramachandrappa B K Nanjappa H V 2004European Journal of Agronomy2004,21,1:1
4Differential expression of MUC genes in endometrial and cervical' tissues and tumors 显示文摘Hebbar V Damera G Sachdev G P 2005BMC Cancer2005,5,:1
5Prognostic value of the type Ⅰ growth factor receptor in a large series of human primary breast cancers quantified with a real-time reverse transcription-polymerase chain reaction assay 显示文摘Pawlowski V Revillion F Hebbar M 2000Clin Cancer Res2000,6,11:1
6Prognostic value of the type Ⅰ growth factor receptors in a large series of human primary breast cancers quantified with a real-time reverse transcriptionpolymerase chain reaction assay显示文摘Pawlowski V Revillion F Hebbar M 2000Clin Cancer Res2000,6,11:1
7Prognostic value of the type I growth factor receptors in a large series of human primary breast cancers quantified with a real-time reverse transcription-polymerase chain reaction assay 显示文摘Pawlowski V Revillion F Hebbar M 2000Clin cancer Res2000,6,11:1
8Resveratrol In- hibits Phorbol Ester and UV-induced Activator Protein 1 Activation by Interfering with Mitogen activated Protein Kinase Pathways显示文摘YU R HEBBAR V KIM D W 2001Molecular Pharmacolo- gy2001,60,1:1
9Prognostic value of the type I growth factor receptors in a large series of human primary breast cancers quantified with a real-time reverse transcription-polymerase chain reaction assay显示文摘PAWLOWSKI V R(E)VILLION F HEBBAR M 2000Clin Cancer Res2000,6,11:1
10In vivo pharmacokinetics and regulation of gene expression profiles by isothioeyanate sulforaphane in the rat显示文摘Hu R Hebbar V Kim BR 2004J Pharmacol Exp Ther2004,310,:1
11Synergistic effects of a combination of dietary factors sulforaphane and(-)epigallocatechin-3-gallate in HT-29 AP-1human colon carcinoma cells显示文摘Nair S Hebbar V Shen G 2008Pharm Res2008,25,2:1
12Studies on NPK drip fertigation in field grown tomato ( Lycopersicon escu- lentum Mill) 显示文摘Hebbar S S Ramachandrappa B K Nanjappa H V 2004European Journal of Agronomy2004,21,1:1
13Metabolism,oral bioavailability and pharmacokinetics of chemopreventive kaempferol in rats显示文摘Barve A Chen C Hebbar V 2009Biopharm Drug Dispos2009,30,7:1
14Differential expression of MUC genes in endometrial and cervical tissues and tumors显示文摘Hebbar V Damera G Sachdev GP 2005BMC Cancer2005,5,1:1
15Prognostic value of the type 1 growth factor receptors in a large series of hu-man primary breast cancers quantified with a real-time re-verse transcription-polymerase chain reaction assay显示文摘Pawlowski V Revillion F Hebbar M 2000Clin Cancer Res2000,6,11:1
16In vivo pharmacokinetics and regulation of gene expression profiles by isothiocyanate sulforaphane in the rat 显示文摘Hu R Hebbar V Kim BR 2004J Pharmacol Exp Ther2004,310,:1
17Resveratrol inhibits phorbolester and UV-induced activator protein 1 activation by interfering with mitogen-activated protein kinase pathways 显示文摘Yu R Hebbar V Kim DW 2001Mol Pharmacol2001,60,1:1
18Resveratrol inhibits phorbol ester and UV-induced activator protein 1 activation by interfering with mitogen-activated protein kinase pathways 显示文摘Yu R Hebbar V Kim DW 2001Molecular Pharmacol2001,60,1:1
19Synergistic effects of a combination of dietary factors sulforaphane and (-) epigallocatechin-3-gallate in HT-29 AP-1 human colon carcinoma cells显示文摘Nair S Hebbar V Shen G 2008Pharm Res2008,25,2:1
20In vivo pharmacokinetics and reg- ulation of gene expression profiles by isothiocyanate sulforaphane in the rat 显示文摘Hu R Hebbar V Kim BR 2004J Pharmacol Exp Ther2004,310,1:1
返回顶部 每页显示:
共3页 首页 上一页 第1页 下一页 末页 /3 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费