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Inherited Cardiomyopathies

Circulation Journal, 2014/09/25, Vol.78(10), pp.2347-2356

Towbin, Jeffrey A.

2014

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Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism

Circulation research, 2017-09, Vol.121 (7), p.838-854

2017

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Left ventricular non-compaction cardiomyopathy

The Lancet (British edition), 2015-08, Vol.386 (9995), p.813-825

2015

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Dilated cardiomyopathy

The Lancet (British edition), 2010-02, Vol.375 (9716), p.752-762

2010

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Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2016-12, Vol.134 (23), p.e579-e646

2016

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Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2009-07, Vol.54 (3), p.201-211

2009

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Cardiovascular Health Promotion in Children: Challenges and Opportunities for 2020 and Beyond: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2016-09, Vol.134 (12), p.e236-e255

2016

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Pediatric Cardiomyopathies

Circulation research, 2017-09, Vol.121 (7), p.855-873

2017

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Association between diffuse myocardial fibrosis and diastolic dysfunction in sickle cell anemia

Blood, 2017-07, Vol.130 (2), p.205-213

2017

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Pediatric Primary Dilated Cardiomyopathy Gene Testing and Variant Reclassification: Does It Matter?

Journal of the American Heart Association, 2020-06, Vol.9 (11), p.e016910-e016910

Towbin, Jeffrey A

2020

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Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline

Journal of cardiac failure, 2009-03, Vol.15 (2), p.83-97

2009

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Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

Proceedings of the National Academy of Sciences - PNAS, 2011-02, Vol.108 (7), p.2915-2920

2011

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Mortality and Sudden Death in Pediatric Left Ventricular Noncompaction in a Tertiary Referral Center

Circulation (New York, N.Y.), 2013-06, Vol.127 (22), p.2202-2208

2013

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Prevalence, Morbidity, and Mortality of Heart Failure–Related Hospitalizations in Children in the United States: A Population-Based Study

Journal of cardiac failure, 2012-06, Vol.18 (6), p.459-470

2012

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Autism Spectrum Disorder Scale Scores in Pediatric Mood and Anxiety Disorders

Journal of the American Academy of Child and Adolescent Psychiatry, 2008-06, Vol.47 (6), p.652-661

2008

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Ionic Mechanisms Responsible for the Electrocardiographic Phenotype of the Brugada Syndrome Are Temperature Dependent

Circulation research, 1999-10, Vol.85 (9), p.803-809

1999

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Endorsement of Health and Human Services recommendation for pulse oximetry screening for critical congenital heart disease

Pediatrics (Evanston), 2012-01, Vol.129 (1), p.190

2012

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Cardiac metabolic pathways affected in the mouse model of barth syndrome

PloS one, 2015-06, Vol.10 (6), p.e0128561-e0128561

2015

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The failing heart

Nature (London), 2002-01, Vol.415 (6868), p.227-233

2002

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Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

The New England journal of medicine, 2008-05, Vol.358 (18), p.1899-1908

2008

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Hot Topics in Tetralogy of Fallot

Journal of the American College of Cardiology, 2013-12, Vol.62 (23), p.2155-2166

2013

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Left ventricular noncompaction: a new form of heart failure

Heart failure clinics, 2010-10, Vol.6 (4), p.453

Towbin, Jeffrey A

2010

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The effects of cardio-selective β blockade on diastolic dysfunction in children with sickle cell disease

Haematologica (Roma), 2023-02, Vol.108 (2), p.594

2023

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Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention

Circulation (New York, N.Y.), 2006-04, Vol.113 (14), p.1807-1816

2006

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Inherited Cardiomyopathies

Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism

Left ventricular non-compaction cardiomyopathy

Dilated cardiomyopathy

Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association

Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy

Cardiovascular Health Promotion in Children: Challenges and Opportunities for 2020 and Beyond: A Scientific Statement From the American Heart Association

Pediatric Cardiomyopathies

Association between diffuse myocardial fibrosis and diastolic dysfunction in sickle cell anemia

Pediatric Primary Dilated Cardiomyopathy Gene Testing and Variant Reclassification: Does It Matter?

Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline

Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

Mortality and Sudden Death in Pediatric Left Ventricular Noncompaction in a Tertiary Referral Center

Prevalence, Morbidity, and Mortality of Heart Failure–Related Hospitalizations in Children in the United States: A Population-Based Study

Autism Spectrum Disorder Scale Scores in Pediatric Mood and Anxiety Disorders

Ionic Mechanisms Responsible for the Electrocardiographic Phenotype of the Brugada Syndrome Are Temperature Dependent

Endorsement of Health and Human Services recommendation for pulse oximetry screening for critical congenital heart disease

Cardiac metabolic pathways affected in the mouse model of barth syndrome

The failing heart

Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

Hot Topics in Tetralogy of Fallot

Left ventricular noncompaction: a new form of heart failure

The effects of cardio-selective β blockade on diastolic dysfunction in children with sickle cell disease

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