J. Larrañaga-Moreira

发表

The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals.

P. Elliott, L. Monserrat, J. Ochoa, 2020, European journal of medical genetics.

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

R. Yotti, L. Monserrat, J. Ochoa, 2020, Revista espanola de cardiologia.

Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction.

D. Andreini, G. Pontone, J. Bogaert, 2021, Journal of the American College of Cardiology.

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

M. Crespo-Leiro, R. Barriales-Villa, J. Larrañaga-Moreira, 2021, Revista espanola de cardiologia.

Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene

D. Fatkin, P. Elliott, J. Mogensen, 2020, Circulation. Heart failure.

Diagnostic and prognostic value of cardiac imaging in amyloidosis

M. Crespo-Leiro, J. Larrañaga-Moreira, R. Vidal-Perez, 2020, World journal of cardiology.

Trends in referral patterns, invasive management, and mortality in elderly patients referred for exercise stress testing.

J. Peteiro, J. Larrañaga-Moreira, A. Bouzas-Mosquera, 2015, European journal of internal medicine.

Classification of Pulmonary Arterial Hypertension by Genetic and Familial Testing.

M. Crespo-Leiro, M. Paniagua-Martín, R. Barriales-Villa, 2019, Revista espanola de cardiologia.

Value of a comprehensive exercise echocardiography assessment for patients with hypertrophic cardiomyopathy.

L. Monserrat, J. Peteiro, R. Barriales-Villa, 2020, Journal of cardiology.

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

R. Barriales-Villa, J. Larrañaga-Moreira, I. Cárdenas-Reyes, 2019, Revista espanola de cardiologia.

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

P. Elliott, J. Mogensen, M. Pavlou, 2021, JAMA cardiology.

Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator

C. Basso, J. Mogensen, M. Pavlou, 2022, European heart journal.

Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy.

A. Bayés‐Genís, F. Domínguez, E. González-López, 2021, Journal of the American College of Cardiology.

Prevalence and clinical outcomes of dystrophin‐associated dilated cardiomyopathy without severe skeletal myopathy

R. Brugada, D. Freimark, J. Mogensen, 2021, European journal of heart failure.

Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy

L. Mestroni, S. Heymans, R. Brugada, 2022, Journal of the American College of Cardiology.

Hypokinetic hypertrophic cardiomyopathy: clinical phenotype, genetics, and prognosis

D. Freimark, A. Sabbag, R. Barriales-Villa, 2022, ESC heart failure.

The effect of age and sex on the diagnostic yield of the echocardiogram in patients with syncope.

J. Larrañaga-Moreira, A. Bouzas-Mosquera, C. Barbeito-Caamaño, 2019, Revista clinica espanola.

Letter by Barriales-Villa et al Regarding Article, "Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies".

J. Ochoa, R. Barriales-Villa, J. Larrañaga-Moreira, 2019, Circulation.

Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant.

X. Fernandez, D. Brito, T. Ripoll-Vera, 2021, Revista espanola de cardiologia.

Mitral valve prolapse morphofunctional features by cardiovascular magnetic resonance: more than just a valvular disease

J. Sanz, B. Ibáñez, A. Chokshi, 2021, Journal of Cardiovascular Magnetic Resonance.

iPSC-Based Modeling of Variable Clinical Presentation in Hypertrophic Cardiomyopathy

Á. Raya, J. L. de la Pompa, L. Monserrat, 2023, Circulation research.

Ventricular arrhythmias in hypertrophic cardiomyopathy patients: prevalence, distribution, predictors and outcome.

A. Sabbag, A. Segev, R. Barriales-Villa, 2023, Heart rhythm.

Incidental finding of cornea verticillata or lamellar inclusions in kidney biopsy: measurement of lyso-Gb3 in plasma defines between Fabry disease and drug-induced phospholipidosis.

J. Politei, A. Schenone, R. Barriales-Villa, 2020, Biochimica et biophysica acta. Molecular basis of disease.

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

Thomas A. Slater, L. Mestroni, D. Fatkin, 2023, Circulation. Genomic and precision medicine.

Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives.

J. Rodríguez-Palomares, M. Sabater-Molina, T. Ripoll-Vera, 2024, Journal of the American College of Cardiology.

Value of a comprehensive exercise echocardiography assessment for patients with hypertrophic cardiomyopathy.

L. Monserrat, J. Peteiro, R. Barriales-Villa, 2020, Journal of cardiology.

Late gadolinium enhancement distribution patterns in non-ischaemic dilated cardiomyopathy: genotype–phenotype correlation

A. Bayés‐Genís, P. García-Pavía, J. Rodríguez-Palomares, 2023, European heart journal. Cardiovascular Imaging.

Impact of SARS-CoV-2 infection in patients with cardiac amyloidosis: Results of a multicentre registry.

R. Barriales-Villa, J. Larrañaga-Moreira, E. Zorio, 2023, Medicina clinica.

Gender variability in the clinical phenotype of hypertrophic cardiomyopathy

D. Freimark, L. Monserrat, A. Sabbag, 2020 .