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Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene

BMC medical genetics, 2008-10, Vol.9 (1), p.95-95

2008

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Biophysical characterization of KCNQ1 P320 mutations linked to long QT syndrome 1

Journal of molecular and cellular cardiology, 2010-01, Vol.48 (1), p.230-237

2010

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Improved troponin T ELISA specific for cardiac troponin T isoform: assay development and analytical and clinical validation

Clinical chemistry (Baltimore, Md.), 1997-03, Vol.43 (3), p.458-466

1997

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Heart rate reduction after heart transplantation with beta-blocker versus the selective If channel antagonist ivabradine

Transplantation, 2007-10, Vol.84 (8), p.988-996

2007

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Absence of auto-antibodies against cardiac troponin I predicts improvement of left ventricular function after acute myocardial infarction

European heart journal, 2008-08, Vol.29 (16), p.1949-1955

2008

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cAMP Sensitivity of HCN Pacemaker Channels Determines Basal Heart Rate But Is Not Critical for Autonomic Rate Control

Circulation. Arrhythmia and electrophysiology, 2010-10, Vol.3 (5), p.542-552

2010

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Cardiac troponin T in patients with end-stage renal disease: absence of expression in truncal skeletal muscle

Clinical chemistry (Baltimore, Md.), 1998-05, Vol.44 (5), p.930-938

1998

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The Novel cAMP-Insensitive HCN4-695X Mutation is Associated with Marked Sinus Bradycardia but Regular Autonomic Rate Control

Biophysical journal, 2011-02, Vol.100 (3), p.105a-105a

2011

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Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein

The Journal of clinical investigation, 1997-07, Vol.100 (2), p.475-482

1997

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Abstract 2425: Absence of Auto-Antibodies against Cardiac Troponin I Predicts Improvement of Left Ventricular Function after Acute Myocardial Infarction

Circulation (New York, N.Y.), 2008-10, Vol.118 (suppl_18)

2008

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Cardiac-specific activation of Cre expression at late fetal development

Biochemical and biophysical research communications, 2007-07, Vol.359 (2), p.209-213

2007

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Elevated serum concentrations of cardiac troponin T in acute allograft rejection after human heart transplantation

Journal of the American College of Cardiology, 1998-08, Vol.32 (2), p.405-412

1998

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Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3gene

BMC medical genetics, 2008-10, Vol.9 (1), Article 95

2008

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Identification and genotype related classification of children with long QT-syndrome using 24 h Holter recordings

Studies in health technology and informatics, 2007, Vol.129 (Pt 2), p.1299

2007

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Molecular cloning and expression of cERG, the ether à go-go-related gene from canine myocardium

Pflügers Archiv, 2001-05, Vol.442 (2), p.188-191

2001

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Trapping and Metabolism of Radioiodinated PHIPA 3-10 in the Rat Myocardium

The Journal of nuclear medicine (1978), 1997-12, Vol.38 (12), p.1864-1869

1997

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Prognostic impact of thallium scintigraphy and exercise capacity in chronic coronary artery disease: A 10 years follow-up

Journal of nuclear cardiology, 1999, Vol.6 (1), p.S94-S94

1999

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Dipyridamole Thallium imaging after emergency coronary stenting: Increased restenosis at follow-up in patients with irreversible tracer defects

Journal of nuclear cardiology, 1995-03, Vol.2 (2), p.S86-S86

1995

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I-123 PHIPA scintigraphy in chronic coronary artery disease: A comparative study with TL-201

Journal of nuclear cardiology, 1995-03, Vol.2 (2), p.S98-S98

1995

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Computer based modeling of the congenital long-QT 2 syndrome in the Visible Man torso: From genes to ECG

2007 29th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, 2007, Vol.2007, p.1410-1413

2007

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Wertigkeit myofibrillärer Proteine in der Diagnostik des akuten Myokardinfarktes

Pathobiochemie, Molekularbiologie und moderne Diagnostik kardiovaskulärer Erkrankungen, p.154-164

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Residual 201 Tl Activity in Irreversible Defects as a Marker of Myocardial Viability: Clinicopathological Study

Circulation (New York, N.Y.), 1995-02, Vol.91 (4), p.1016-1021

1995

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Residual 201Tl activity in irreversible defects as a marker of myocardial viability : clinicopathological study

Circulation (New York, N.Y.), 1995-02, Vol.91 (4), p.1016-1021

1995

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Design of a full SiC three-phase power factor correction with an interleaved output buck converter

Journal of engineering (Stevenage, England), 2019-06, Vol.2019 (17), p.4143-4146

2019

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Leakage current reduction for a double-leg boost converter by switching transition synchronisation

Journal of engineering (Stevenage, England), 2019-06, Vol.2019 (17), p.3789-3792

2019

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Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene

Biophysical characterization of KCNQ1 P320 mutations linked to long QT syndrome 1

Improved troponin T ELISA specific for cardiac troponin T isoform: assay development and analytical and clinical validation

Heart rate reduction after heart transplantation with beta-blocker versus the selective If channel antagonist ivabradine

Absence of auto-antibodies against cardiac troponin I predicts improvement of left ventricular function after acute myocardial infarction

cAMP Sensitivity of HCN Pacemaker Channels Determines Basal Heart Rate But Is Not Critical for Autonomic Rate Control

Cardiac troponin T in patients with end-stage renal disease: absence of expression in truncal skeletal muscle

The Novel cAMP-Insensitive HCN4-695X Mutation is Associated with Marked Sinus Bradycardia but Regular Autonomic Rate Control

Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein

Abstract 2425: Absence of Auto-Antibodies against Cardiac Troponin I Predicts Improvement of Left Ventricular Function after Acute Myocardial Infarction

Cardiac-specific activation of Cre expression at late fetal development

Elevated serum concentrations of cardiac troponin T in acute allograft rejection after human heart transplantation

Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3gene

Identification and genotype related classification of children with long QT-syndrome using 24 h Holter recordings

Molecular cloning and expression of cERG, the ether à go-go-related gene from canine myocardium

Trapping and Metabolism of Radioiodinated PHIPA 3-10 in the Rat Myocardium

Prognostic impact of thallium scintigraphy and exercise capacity in chronic coronary artery disease: A 10 years follow-up

Dipyridamole Thallium imaging after emergency coronary stenting: Increased restenosis at follow-up in patients with irreversible tracer defects

I-123 PHIPA scintigraphy in chronic coronary artery disease: A comparative study with TL-201

Computer based modeling of the congenital long-QT 2 syndrome in the Visible Man torso: From genes to ECG

Wertigkeit myofibrillärer Proteine in der Diagnostik des akuten Myokardinfarktes

Residual 201 Tl Activity in Irreversible Defects as a Marker of Myocardial Viability: Clinicopathological Study

Residual 201Tl activity in irreversible defects as a marker of myocardial viability : clinicopathological study

Design of a full SiC three-phase power factor correction with an interleaved output buck converter

Leakage current reduction for a double-leg boost converter by switching transition synchronisation

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