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Long P-wave duration immediately after pulmonary vein isolation on radiofrequency catheter ablation for atrial fibrillation predicts clinical recurrence: correlation with atrial remodeling in persistent atrial fibrillation.
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- Heart & Vessels, 2022, v. 37, n. 3, p. 476, doi. 10.1007/s00380-021-01932-w
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- Article
Combined Prognostic Impact of Two Quick Frailty Assessments in Acute Heart Failure.
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- Gerontology, 2024, v. 70, n. 3, p. 248, doi. 10.1159/000534757
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- Article
Prognostic efficacy of a post-discharge visiting program for patients with heart failure.
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- Nagoya Journal of Medical Science, 2022, v. 84, n. 4, p. 723, doi. 10.18999/nagjms.84.4.723
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Prognostic utility of multipoint nutritional screening for hospitalized patients with acute decompensated heart failure.
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- Nagoya Journal of Medical Science, 2021, v. 83, n. 1, p. 93, doi. 10.18999/nagjms.83.1.93
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- Article
Oxido-reductive regulation of vascular remodeling by receptor tyrosine kinase ROS1.
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- Journal of Clinical Investigation, 2014, v. 124, n. 12, p. 5159, doi. 10.1172/JCI77484
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- Article
Identification of <italic>CDC42BPG</italic> as a novel susceptibility locus for hyperuricemia in a Japanese population.
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- Molecular Genetics & Genomics, 2018, v. 293, n. 2, p. 371, doi. 10.1007/s00438-017-1394-1
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- Article
Outcomes and Safety of Very-Low-Dose Edoxaban in Frail Patients With Atrial Fibrillation in the ELDERCARE-AF Randomized Clinical Trial.
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- JAMA Network Open, 2022, v. 5, n. 8, p. e2228500, doi. 10.1001/jamanetworkopen.2022.28500
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- Article
Pathophysiology of ‘Tako-Tsubo’ cardiomyopathy: collecting pieces of a puzzle: reply.
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- European Heart Journal, 2008, v. 29, n. 8, p. 1072, doi. 10.1093/eurheartj/ehn065
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- Article
Association of a Polymorphism of BTN2A1 With Hypertension in Japanese Individuals.
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- American Journal of Hypertension, 2011, v. 24, n. 8, p. 924, doi. 10.1038/ajh.2011.74
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- Article
Assessment of a Polymorphism of SDK1 With Hypertension in Japanese Individuals.
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- American Journal of Hypertension, 2010, v. 23, n. 1, p. 70, doi. 10.1038/ajh.2009.190
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- Article
Assessment of Genetic Risk Factors for Thoracic Aortic Aneurysm in Hypertensive Patients.
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- American Journal of Hypertension, 2008, v. 21, n. 9, p. 1023, doi. 10.1038/ajh.2008.229
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- Article
Regional left atrial conduction velocity in the anterior wall is associated with clinical recurrence of atrial fibrillation after catheter ablation: efficacy in combination with the ipsilateral low voltage area.
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- BMC Cardiovascular Disorders, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12872-022-02881-6
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- Article
Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population.
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- Biomedical Reports, 2018, v. 9, n. 5, p. 383, doi. 10.3892/br.2018.1152
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- Article
Six novel susceptibility loci for coronary artery disease and cerebral infarction identified by longitudinal exome-wide association studies in a Japanese population.
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- Biomedical Reports, 2018, v. 9, n. 2, p. 123, doi. 10.3892/br.2018.1109
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- Article
Identification of four genes as novel susceptibility loci for early-onset type 2 diabetes mellitus, metabolic syndrome, or hyperuricemia.
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- Biomedical Reports, 2018, v. 9, n. 1, p. 21, doi. 10.3892/br.2018.1105
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Identification of nine genes as novel susceptibility loci for early-onset ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage.
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- Biomedical Reports, 2018, v. 9, n. 1, p. 8, doi. 10.3892/br.2018.1104
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Association of smoking with prevalence of common diseases and metabolic abnormalities in community-dwelling Japanese individuals.
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- Biomedical Reports, 2017, v. 7, n. 5, p. 429, doi. 10.3892/br.2017.991
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- Article
Association of renal function with clinical parameters and conditions in a longitudinal population-based epidemiological study.
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- Biomedical Reports, 2017, v. 6, n. 2, p. 242, doi. 10.3892/br.2016.831
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Association of genetic variants with atrial fibrillation.
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- Biomedical Reports, 2016, v. 4, n. 2, p. 178, doi. 10.3892/br.2015.551
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Association of FURIN and ZPR1 polymorphisms with metabolic syndrome.
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- Biomedical Reports, 2015, v. 3, n. 5, p. 641, doi. 10.3892/br.2015.484
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Association of FURIN and ZPR1 polymorphisms with metabolic syndrome.
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- Biomedical Reports, 2015, p. 641, doi. 10.3892/br.2015.484
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Association of TOMM40 and SLC22A4 polymorphisms with ischemic stroke.
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- Biomedical Reports, 2015, v. 3, n. 4, p. 491, doi. 10.3892/br.2015.457
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Association of genetic variants of the a-kinase 1 gene with type 2 diabetes mellitus in a longitudinal population-based genetic epidemiological study.
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- Biomedical Reports, 2015, v. 3, n. 3, p. 347, doi. 10.3892/br.2015.439
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Association of a transcription factor 21 gene polymorphism with hypertension.
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- Biomedical Reports, 2015, v. 3, n. 1, p. 118, doi. 10.3892/br.2014.371
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Association of a genetic variant of the ZPR1 zinc finger gene with type 2 diabetes mellitus.
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- Biomedical Reports, 2015, v. 3, n. 1, p. 88, doi. 10.3892/br.2014.379
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Association of genetic variants of the α-kinase 1 gene with myocardial infarction in community-dwelling individuals.
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- Biomedical Reports, 2014, v. 2, n. 1, p. 127, doi. 10.3892/br.2013.190
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- Article
Association between polymorphisms of the α-kinase 1 gene and type 2 diabetes mellitus in community-dwelling individuals.
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- Biomedical Reports, 2013, v. 1, n. 6, p. 940, doi. 10.3892/br.2013.173
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- Article
Association of a polymorphism of BTN2A1 with chronic kidney disease in community-dwelling individuals.
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- Biomedical Reports, 2013, v. 1, n. 6, p. 868, doi. 10.3892/br.2013.176
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- Article
Association of genetic variants of CELSR1 and 3q28 with hypertension in community-dwelling individuals.
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- Biomedical Reports, 2013, v. 1, n. 6, p. 840, doi. 10.3892/br.2013.168
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Association of a polymorphism of the interleukin 6 receptor gene with chronic kidney disease in Japanese individuals.
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- Nephrology, 2015, v. 20, n. 4, p. 273, doi. 10.1111/nep.12381
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- Article
Identification of TNFSF13, SPATC1L, SLC22A25 and SALL4 as novel susceptibility loci for atrial fibrillation by an exome‑wide association study.
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- Molecular Medicine Reports, 2017, v. 16, n. 5, p. 5823, doi. 10.3892/mmr.2017.7334
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Association of genetic variants with dyslipidemia.
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- Molecular Medicine Reports, 2015, v. 12, n. 4, p. 5429, doi. 10.3892/mmr.2015.4081
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- Article
Association of a polymorphism of BTN2A1 with dyslipidemia in community-dwelling individuals.
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- Molecular Medicine Reports, 2014, v. 9, n. 3, p. 808, doi. 10.3892/mmr.2014.1902
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- Article
Combined prognostic value of malnutrition using GLIM criteria and renal insufficiency in elderly heart failure.
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- ESC Heart Failure, 2022, v. 9, n. 1, p. 704, doi. 10.1002/ehf2.13685
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Evolutionary history of disease‐susceptibility loci identified in longitudinal exome‐wide association studies.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.925
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Reduction of door‐to‐balloon time in patients with ST‐elevation myocardial infarction by single‐catheter primary percutaneous coronary intervention method.
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- Catheterization & Cardiovascular Interventions, 2022, v. 99, n. 2, p. 314, doi. 10.1002/ccd.29797
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Association of a genetic variant of BTN2A1 with chronic kidney disease in Japanese individuals.
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- Nephrology, 2011, v. 16, n. 7, p. 642, doi. 10.1111/j.1440-1797.2011.01470.x
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- Article
Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia.
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- International Journal of Molecular Medicine, 2019, v. 43, n. 1, p. 57, doi. 10.3892/ijmm.2018.3943
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Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease.
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- International Journal of Molecular Medicine, 2018, v. 42, n. 5, p. 2415, doi. 10.3892/ijmm.2018.3852
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- Article
Identification of novel hyper- or hypomethylated CpG sites and genes associated with atherosclerotic plaque using an epigenome-wide association study.
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- International Journal of Molecular Medicine, 2018, v. 41, n. 5, p. 2724, doi. 10.3892/ijmm.2018.3453
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- Article
Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies.
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- International Journal of Molecular Medicine, 2017, v. 39, n. 6, p. 1477, doi. 10.3892/ijmm.2017.2972
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- Article
Identification of EGFLAM, SPATC1L and RNASE13 as novel susceptibility loci for aortic aneurysm in Japanese individuals by exome-wide association studies.
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- International Journal of Molecular Medicine, 2017, v. 39, n. 5, p. 1091, doi. 10.3892/ijmm.2017.2927
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- Article
Association of six genetic variants with myocardial infarction.
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- International Journal of Molecular Medicine, 2015, v. 35, n. 5, p. 1451, doi. 10.3892/ijmm.2015.2115
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- Article
Association of genetic variants with hypertension in a longitudinal population-based genetic epidemiological study.
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- International Journal of Molecular Medicine, 2015, v. 35, n. 5, p. 1189, doi. 10.3892/ijmm.2015.2151
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- Article
Identification of hypo- and hypermethylated genes related to atherosclerosis by a genome-wide analysis of DNA methylation.
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- International Journal of Molecular Medicine, 2014, v. 33, n. 5, p. 1355, doi. 10.3892/ijmm.2014.1692
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- Article
Impact of matrix metalloproteinase-2 levels on long-term outcome following pharmacological or electrical cardioversion in patients with atrial fibrillation.
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- EP: Europace, 2009, v. 11, n. 3, p. 332, doi. 10.1093/europace/eun389
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- Article