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A cost-effectiveness analysis of hypertrophic cardiomyopathy sudden cardiac death risk algorithms for implantable cardioverter defibrillator decision-making

European heart journal. Quality of care & clinical outcomes, 2024-06, Vol.10 (4), p.285-293

2024

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Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure

JAMA cardiology, 2021-08, Vol.6 (8), p.891

2021

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Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy

JACC. Clinical electrophysiology, 2024-06, Vol.10 (6), p.1178-1190

2024

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2023 ESC Guidelines for the management of cardiomyopathies

Giornale italiano di cardiologia (2006), 2023-11, Vol.24 (11 Suppl 1), p.e1

2023

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ROD2 domain filamin C missense mutations exhibit a distinctive cardiac phenotype with restrictive/hypertrophic cardiomyopathy and saw-tooth myocardium

Revista española de cardiología (English ed.), 2023-05, Vol.76 (5), p.301-311

2023

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First Reported Case of Fabry Disease Caused by a Somatic Mosaicism in the GLA Gene

Revista española de cardiología (English ed.), 2019-07, Vol.72 (7), p.585-587

2019

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Comments on the 2014 ESC Guidelines on the Diagnosis and Management of Hypertrophic Cardiomyopathy. A Critical View From the Perspective of Spanish Cardiology

Revista española de cardiología (English ed.), 2015-01, Vol.68 (1), p.4-9

2015

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The p.Arg118Cys Variant in the GLA Gene Does Not Cause Fabry Disease. More Evidence

Revista española de cardiología (English ed.), 2018-10, Vol.71 (10), p.871-873

2018

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Bicuspid aortic valve and coronary anomalies

Circulation (New York, N.Y.), 2003-04, Vol.107 (16), p.e105; author reply e105-e105; author reply e105

2003

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Plan of Action for Inherited Cardiovascular Diseases: Synthesis of Recommendations and Action Algorithms

Revista española de cardiología (English ed.), 2016-03, Vol.69 (3), p.300-309

2016

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Treatment of hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 2003-04, Vol.107 (16), p.e110; auhor reply e110-e110; auhor reply e110

2003

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Hypertrophic Cardiomyopathy Without Ventricular Hypertrophy: Usefulness of Genetic and Pathological Study in Preventing Sudden Death

Revista española de cardiología (English ed.), 2017-07, Vol.70 (7), p.604-606

2017

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Cardiac-only Timothy Syndrome (COTS): Peripartum Cardiomyopathy and Long QT Syndrome

Revista española de cardiología (English ed.), 2019-10, Vol.72 (10), p.876-878

2019

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Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry

Revista española de cardiología (English ed.), 2021-03, Vol.74 (3), p.216-224

2021

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Coronary anomalies

Circulation (New York, N.Y.), 2003-02, Vol.107 (5), p.E36-6; author reply E36-6

2003

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Do racial or populational differences exist in coronary anomalies?

International journal of cardiology, 2001-11, Vol.81 (1), p.89-90

2001

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The Importance of Family-genetic Screening: The Phenotype Caused by the p.L3778F Ryanodine Receptor Mutation is Likely Less Severe Than Previously Thought

Revista española de cardiología (English ed.), 2016-07, Vol.69 (7), p.702-704

2016

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Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic

Human genetics, 2010-04, Vol.127 (4), p.484-484

2010

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Congenital Coronary Artery Anomalies With Origin in the Contralateral Sinus of Valsalva: Which Approach Should We Take?

Revista española de cardiologia, 2006-04, Vol.59 (4), p.360-370

2006

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Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic

Human genetics, 2010-04, Vol.127 (4), p.483-483

2010

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Usefulness of Genetic Diagnosis in a Woman With Hypertrophic Cardiomyopathy and the Desire for Motherhood: Information Is Key

Revista española de cardiología (English ed.), 2014-04, Vol.67 (4), p.333-334

2014

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Brugada syndrome

Revista española de cardiologia, 2010-05, Vol.63 (5), p.620; author reply 620-620; author reply 620

2010

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Severe cardiac conduction disturbances and pacemaker implantation in patients with hypertrophic cardiomyopathy

Revista española de cardiologia, 2010-08, Vol.63 (8), p.985-988

2010

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Pheochromocytoma-Related Cardiomyopathy or Stress Cardiomyopathy Secondary to Pheochromocytoma: Is New Terminology Needed?

Revista española de cardiologia, 2008-04, Vol.61 (4), p.432-433

2008

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A cost-effectiveness analysis of hypertrophic cardiomyopathy sudden cardiac death risk algorithms for implantable cardioverter defibrillator decision-making

Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure

Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy

2023 ESC Guidelines for the management of cardiomyopathies

ROD2 domain filamin C missense mutations exhibit a distinctive cardiac phenotype with restrictive/hypertrophic cardiomyopathy and saw-tooth myocardium

Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants

First Reported Case of Fabry Disease Caused by a Somatic Mosaicism in the GLA Gene

Comments on the 2014 ESC Guidelines on the Diagnosis and Management of Hypertrophic Cardiomyopathy. A Critical View From the Perspective of Spanish Cardiology

The p.Arg118Cys Variant in the GLA Gene Does Not Cause Fabry Disease. More Evidence

Bicuspid aortic valve and coronary anomalies

Plan of Action for Inherited Cardiovascular Diseases: Synthesis of Recommendations and Action Algorithms

Treatment of hypertrophic cardiomyopathy

Hypertrophic Cardiomyopathy Without Ventricular Hypertrophy: Usefulness of Genetic and Pathological Study in Preventing Sudden Death

Cardiac-only Timothy Syndrome (COTS): Peripartum Cardiomyopathy and Long QT Syndrome

Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry

Coronary anomalies

Do racial or populational differences exist in coronary anomalies?

The Importance of Family-genetic Screening: The Phenotype Caused by the p.L3778F Ryanodine Receptor Mutation is Likely Less Severe Than Previously Thought

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic

Congenital Coronary Artery Anomalies With Origin in the Contralateral Sinus of Valsalva: Which Approach Should We Take?

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic

Usefulness of Genetic Diagnosis in a Woman With Hypertrophic Cardiomyopathy and the Desire for Motherhood: Information Is Key

Brugada syndrome

Severe cardiac conduction disturbances and pacemaker implantation in patients with hypertrophic cardiomyopathy

Pheochromocytoma-Related Cardiomyopathy or Stress Cardiomyopathy Secondary to Pheochromocytoma: Is New Terminology Needed?

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