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The prognostic importance of left ventricular outflow obstruction in hypertrophic cardiomyopathy varies in relation to the severity of symptoms

Journal of the American College of Cardiology, 2005-04, Vol.45 (7), p.1076-1080

2005

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Management of hypertrophic cardiomyopathy

BMJ, 2006-05, Vol.332 (7552), p.1251-1255

International edition, 2006

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High Risk for Sudden Death Identified by Electrocardiographic Loop Recording in a Patient With Hypertrophic Cardiomyopathy Without Major Risk Factors

The American journal of cardiology, 2011-05, Vol.107 (10), p.1558-1560

2011

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Prevalence of Anderson–Fabry disease in patients with hypertrophic cardiomyopathy: the European Anderson–Fabry Disease Survey

Heart (British Cardiac Society), 2011-12, Vol.97 (23), p.1957-1960

2011

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Role of echocardiography in acute chest pain syndrome

The American journal of cardiology, 2000-08, Vol.86 (4), p.41-42

2000

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Tissue-Type Plasminogen Activator Therapy Versus Primary Coronary Angioplasty: Impact on Myocardial Tissue Perfusion and Regional Function 1 Month After Uncomplicated Myocardial Infarction

Journal of the American College of Cardiology, 1998-02, Vol.31 (2), p.338-343

1998

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Arterial thrombotic events and acute coronary syndromes with cancer drugs: Are growth factors the missed link? What both cardiologist and oncologist should know about novel angiogenesis inhibitors

International journal of cardiology, 2013-09, Vol.167 (6), p.2421-2429

2013

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Dynamic electrocardiographic changes in patients with arrhythmogenic right ventricular cardiomyopathy

Heart (British Cardiac Society), 2010-04, Vol.96 (7), p.516-522

2010

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Sudden cardiac death in younger adults: autopsy diagnosis as a tool for preventive medicine

Human pathology, 2006-07, Vol.37 (7), p.794-801

2006

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Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates

Human pathology, 2005-07, Vol.36 (7), p.761-767

2005

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Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNAIIe mutation causing hypertrophic cardiomyopathy

Human molecular genetics, 2012, Vol.21 (1), p.85-100

2012

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Assessment and Significance of Left Ventricular Mass by Cardiovascular Magnetic Resonance in Hypertrophic Cardiomyopathy. Commentary

Journal of the American College of Cardiology, 2008, Vol.52 (7), p.559-568

2008

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Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects. Commentary

European heart journal, 2007, Vol.28 (16)

2007

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Limitations of the electrocardiographic diagnosis of left ventricular hypertrophy: the influence of left anterior hemiblock and right bundle branch block

International journal of cardiology, 1992, Vol.34 (1), p.41-48

1992

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Noninvasive assessment of myocardial perfusion: preliminary results in patients with acute myocardial infarction

The American journal of cardiology, 2000-08, Vol.86 (4), p.28-29

2000

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Maternally inherited cardiomyopathy: clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid

Journal of the American College of Cardiology, 1999-05, Vol.33 (6), p.1584-1589

1999

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Familial idiopathic dilated cardiomyopathy

The American heart journal, 1988-04, Vol.115 (4), p.912-914

1988

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Electrocardiographic diagnosis of left ventricular hypertrophy in the presence of left bundle branch block: a wasted effort

International journal of cardiology, 1990-08, Vol.28 (2), p.215-221

1990

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Hyperthrophic cardiomyopathy and the PTPN11 gene

American journal of medical genetics, 2005, Vol.136A (1), p.93-94

2005

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HLA-DR3 antigen linkage in patients with hypertrophic obstructive cardiomyopathy

The American heart journal, 1986, Vol.111 (1), p.91-94

1986

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Antimitochondrial autoantibodies in myocardial hypertrophy: Comparison between hypertrophic cardiomyopathy, hypertensive heart disease, and athlete's heart

The American heart journal, 1988-08, Vol.116 (2), p.496-500

1988

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Equivocal and borderline myocardial hypertrophy in relatives of patients with hypertrophic cardiomyopathy: possible implications in genetics of the disease

Cardiology, 1988, Vol.75 (5), p.348-356

1988

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Prevention of Sudden Cardiac Death With Implantable Cardioverter-Defibrillators in Children and Adolescents With Hypertrophic Cardiomyopathy

The prognostic importance of left ventricular outflow obstruction in hypertrophic cardiomyopathy varies in relation to the severity of symptoms

Management of hypertrophic cardiomyopathy

High Risk for Sudden Death Identified by Electrocardiographic Loop Recording in a Patient With Hypertrophic Cardiomyopathy Without Major Risk Factors

Prevalence of Anderson–Fabry disease in patients with hypertrophic cardiomyopathy: the European Anderson–Fabry Disease Survey

Role of echocardiography in acute chest pain syndrome

Tissue-Type Plasminogen Activator Therapy Versus Primary Coronary Angioplasty: Impact on Myocardial Tissue Perfusion and Regional Function 1 Month After Uncomplicated Myocardial Infarction

Arterial thrombotic events and acute coronary syndromes with cancer drugs: Are growth factors the missed link? What both cardiologist and oncologist should know about novel angiogenesis inhibitors

Dynamic electrocardiographic changes in patients with arrhythmogenic right ventricular cardiomyopathy

Sudden cardiac death in younger adults: autopsy diagnosis as a tool for preventive medicine

Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates

Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNAIIe mutation causing hypertrophic cardiomyopathy

Assessment and Significance of Left Ventricular Mass by Cardiovascular Magnetic Resonance in Hypertrophic Cardiomyopathy. Commentary

Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects. Commentary

Limitations of the electrocardiographic diagnosis of left ventricular hypertrophy: the influence of left anterior hemiblock and right bundle branch block

Noninvasive assessment of myocardial perfusion: preliminary results in patients with acute myocardial infarction

Maternally inherited cardiomyopathy: clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid

Familial idiopathic dilated cardiomyopathy

Electrocardiographic diagnosis of left ventricular hypertrophy in the presence of left bundle branch block: a wasted effort

Hyperthrophic cardiomyopathy and the PTPN11 gene

HLA-DR3 antigen linkage in patients with hypertrophic obstructive cardiomyopathy

Antimitochondrial autoantibodies in myocardial hypertrophy: Comparison between hypertrophic cardiomyopathy, hypertensive heart disease, and athlete's heart

Equivocal and borderline myocardial hypertrophy in relatives of patients with hypertrophic cardiomyopathy: possible implications in genetics of the disease

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