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Predictive value of high-sensitivity troponin for significant coronary artery disease in new-onset atrial fibrillation with rapid ventricular response

Coronary artery disease, 2023-03, Vol.34 (2), p.87

2023

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ANKRD1 , the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene

Journal of the American College of Cardiology, 2009-07, Vol.54 (4), p.325-333

2009

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Natural history and familial characteristics of isolated left ventricular non-compaction

European heart journal, 2005-01, Vol.26 (2), p.187-192

2005

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Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

Human molecular genetics, 2012-05, Vol.21 (9), p.2039-2053

2012

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Current status of vulnerable plaque detection

Catheterization and cardiovascular interventions, 2010-01, Vol.75 (1), p.135-144

2010

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Epigenetic modulation in the treatment of atherosclerotic disease

Frontiers in genetics, 2014, Vol.5, p.364-364

2014

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Mitral Valve Abnormalities in Hypertrophic Cardiomyopathy: Echocardiographic Features and Surgical Outcomes

The Annals of thoracic surgery, 2008-05, Vol.85 (5), p.1527-1535.e2

2008

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The use of deformation imaging in the assessment of patients pre and post transcatheter aortic valve implantation

Echo research and practice, 2023-02, Vol.10 (1), p.3-3, Article 3

2023

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CT coronary angiography and COVID-19: inpatient use in acute chest pain service

Open heart, 2021-03, Vol.8 (1), p.e001548

2021

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Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

Journal of the American College of Cardiology, 2010-10, Vol.56 (18), p.1493-1502

2010

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Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

The Lancet (British edition), 2004-01, Vol.363 (9406), p.371-372

2004

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Myocardial strain: a clinical review

Irish journal of medical science, 2023-08, Vol.192 (4), p.1649-1656

2023

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Subclinical anthracycline- and trastuzumab-induced cardiotoxicity in the long-term follow-up of asymptomatic breast cancer survivors: a speckle tracking echocardiographic study

Heart (British Cardiac Society), 2010-05, Vol.96 (9), p.701-707

2010

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Improvements in cardiac function detected using echocardiography in patients with hereditary haemochromatosis

Irish journal of medical science, 2020-02, Vol.189 (1), p.109-117

2020

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Mutations in PDLIM3 and MYOZ1 encoding myocyte Z line proteins are infrequently found in idiopathic dilated cardiomyopathy

Molecular genetics and metabolism, 2007-04, Vol.90 (4), p.435-440

2007

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Cardiac Magnetic Resonance at 3.0 T in Patients With C282Y Homozygous Hereditary Hemochromatosis: Superiority of Radial and Circumferential Strain Over Cardiac T2 Measurements at Baseline and at Post Venesection Follow-up

Journal of thoracic imaging, 2022-09, Vol.37 (5), p.300-306

2022

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Long-term Outcomes for Drug-eluting Balloons versus Drug-eluting Stents in the Treatment of Small Vessel Coronary Artery Disease: A Systematic Review and Meta-analysis

Interventional cardiology (London), 2023-01, Vol.18

2023

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Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

Journal of the American College of Cardiology, 2004-11, Vol.44 (10), p.2033-2040

2004

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Mutations in Cypher/ZASP in patients with Dilated cardiomyopathy and left ventricular non-compaction

Journal of the American College of Cardiology, 2003-12, Vol.42 (11), p.2014-2027

2003

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Tissue Synchronization Imaging and Optimal Left Ventricular Pacing Site in Cardiac Resynchronization Therapy

The American journal of cardiology, 2006-06, Vol.97 (11), p.1615-1621

2006

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Ventricular Activation Time as a Marker for Diastolic Dysfunction in Early Hypertension

American journal of hypertension, 2010-07, Vol.23 (7), p.781-785

2010

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Prospective familial assessment in dilated cardiomyopathy : Cardiac autoantibodies predict disease development in asymptomatic relatives

Circulation (New York, N.Y.), 2007-01, Vol.115 (1), p.76-83

2007

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Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease

Annals of internal medicine, 2005-07, Vol.143 (2), p.108

2005

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A case report of ventricular septal defect complicating transcatheter aortic valve implant for aortic regurgitation: novel complication and technical considerations

European heart journal : case reports, 2021-10, Vol.5 (10), p.ytab387

2021

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Predictive value of high-sensitivity troponin for significant coronary artery disease in new-onset atrial fibrillation with rapid ventricular response

ANKRD1 , the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene

Natural history and familial characteristics of isolated left ventricular non-compaction

Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

Current status of vulnerable plaque detection

Epigenetic modulation in the treatment of atherosclerotic disease

Mitral Valve Abnormalities in Hypertrophic Cardiomyopathy: Echocardiographic Features and Surgical Outcomes

The use of deformation imaging in the assessment of patients pre and post transcatheter aortic valve implantation

CT coronary angiography and COVID-19: inpatient use in acute chest pain service

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

Interhospital and interindividual variability in secondary prevention: a comparison of outpatients with a history of chronic coronary syndrome versus outpatients with a history of acute coronary syndrome (the iASPIRE Study)

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

Myocardial strain: a clinical review

Subclinical anthracycline- and trastuzumab-induced cardiotoxicity in the long-term follow-up of asymptomatic breast cancer survivors: a speckle tracking echocardiographic study

Improvements in cardiac function detected using echocardiography in patients with hereditary haemochromatosis

Mutations in PDLIM3 and MYOZ1 encoding myocyte Z line proteins are infrequently found in idiopathic dilated cardiomyopathy

Cardiac Magnetic Resonance at 3.0 T in Patients With C282Y Homozygous Hereditary Hemochromatosis: Superiority of Radial and Circumferential Strain Over Cardiac T2 Measurements at Baseline and at Post Venesection Follow-up

Long-term Outcomes for Drug-eluting Balloons versus Drug-eluting Stents in the Treatment of Small Vessel Coronary Artery Disease: A Systematic Review and Meta-analysis

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

Mutations in Cypher/ZASP in patients with Dilated cardiomyopathy and left ventricular non-compaction

Tissue Synchronization Imaging and Optimal Left Ventricular Pacing Site in Cardiac Resynchronization Therapy

Ventricular Activation Time as a Marker for Diastolic Dysfunction in Early Hypertension

Prospective familial assessment in dilated cardiomyopathy : Cardiac autoantibodies predict disease development in asymptomatic relatives

Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease

A case report of ventricular septal defect complicating transcatheter aortic valve implant for aortic regurgitation: novel complication and technical considerations

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