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Diagnosing transthyretin amyloidosis in patients with known genetic cardiomyopathies – opportunities and open questions. Response

Revista española de cardiología (English ed.), 2024-06, Vol.77 (6), p.505-506

2024

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Anomalous Coronary Arteries Originating in the Contralateral Sinus of Valsalva: Registry of Thirteen Spanish Hospitals (RACES)

Revista española de cardiología (English ed.), 2006-06, Vol.59 (6), p.620-623

2006

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Pregnancy in women with dilated cardiomyopathy genetic variants

Revista española de cardiología (English ed.), 2024-04

2024

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Dilated cardiomyopathy and mild limb girdle muscular dystrophy caused by the p.Gly424Ser genetic variant in the fukutin gene

Revista española de cardiología (English ed.), 2021-11, Vol.74 (11), p.987-989

2021

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Shprintzen-Goldberg syndrome and aortic dilatation: apropos of 2 new cases

Revista española de cardiología (English ed.), 2021-06, Vol.74 (6), p.551-553

2021

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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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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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Mitral Repair as a Treatment of Outflow Tract Obstruction in Hypertrophic Cardiomyopathy: “Myectomy Without Myectomy”

Revista española de cardiología (English ed.), 2019-03, Vol.72 (3), p.266-268

2019

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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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Large Family With Marfan Syndrome Demonstrating the Pathogenicity of a "Synonymous" Variant (p.Ile2118=) in the Fibrillin-1 Gene

Revista española de cardiología (English ed.), 2017-08, Vol.70 (8), p.679-681

2017

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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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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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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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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 cardiología (English ed.), 2010-05, Vol.63 (5), p.620-620

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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Severe Cardiac Conduction Disturbances and Pacemaker Implantation in Patients With Hypertrophic Cardiomyopathy

Revista española de cardiología (English ed.), 2010, Vol.63 (8), p.985-988

2010

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A Homozygous MYBPC3 Gene Mutation Associated With a Severe Phenotype and a High Risk of Sudden Death in a Family With Hypertrophic Cardiomyopathy

Revista española de cardiología (English ed.), 2009-05, Vol.62 (5), p.572-575

2009

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Diagnosing transthyretin amyloidosis in patients with known genetic cardiomyopathies – opportunities and open questions. Response

Anomalous Coronary Arteries Originating in the Contralateral Sinus of Valsalva: Registry of Thirteen Spanish Hospitals (RACES)

Pregnancy in women with dilated cardiomyopathy genetic variants

Dilated cardiomyopathy and mild limb girdle muscular dystrophy caused by the p.Gly424Ser genetic variant in the fukutin gene

Shprintzen-Goldberg syndrome and aortic dilatation: apropos of 2 new cases

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

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

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

Mitral Repair as a Treatment of Outflow Tract Obstruction in Hypertrophic Cardiomyopathy: “Myectomy Without Myectomy”

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

Large Family With Marfan Syndrome Demonstrating the Pathogenicity of a "Synonymous" Variant (p.Ile2118=) in the Fibrillin-1 Gene

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

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

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

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

Brugada Syndrome

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

Severe Cardiac Conduction Disturbances and Pacemaker Implantation in Patients With Hypertrophic Cardiomyopathy

A Homozygous MYBPC3 Gene Mutation Associated With a Severe Phenotype and a High Risk of Sudden Death in a Family With Hypertrophic Cardiomyopathy

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