J. Salazar-Mendiguchía

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.

The influence of aortoseptal angulation on provocable left ventricular outflow tract obstruction in hypertrophic cardiomyopathy

P. Elliott, J. Moon, J. Salazar-Mendiguchía, 2014, Open Heart.

Clinical utility of genetic testing in patients with dilated cardiomyopathy

L. Monserrat, X. Fernandez, J. Ochoa, 2021, Medicina Clínica (English Edition).

Prognostic implications of pathogenic truncating variants in the TTN gene.

L. Monserrat, X. Fernandez, J. Ochoa, 2020, International journal of cardiology.

Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations.

P. Elliott, J. Mogensen, F. Asselbergs, 2018, Journal of the American College of Cardiology.

Genetic Etiology for Alcohol-Induced Cardiac Toxicity

D. O’Regan, S. Cook, J. Ware, 2018, Journal of the American College of Cardiology.

Impact on Delay Times and Characteristics of Patients Undergoing Primary Percutaneous Coronary Intervention in the Southern Metropolitan Area of Barcelona After Implementation of the Infarction Code Program

Á. Cequier, J. Ferreiro, J. Gómez-Lara, 2012 .

Impact on delay times and characteristics of patients undergoing primary percutaneous coronary intervention in the southern metropolitan area of Barcelona after implementation of the infarction code program.

Á. Cequier, J. Ferreiro, J. Gómez-Lara, 2012, Revista espanola de cardiologia.

Clinical Determinants and Prognosis of Left Ventricular Reverse Remodelling in Non-Ischemic Dilated Cardiomyopathy

M. de Antonio, J. Lupón, A. Bayés‐Genís, 2022, Journal of cardiovascular development and disease.

Is it possible to separate ischemic and bleeding risk in patients with non-ST segment elevation acute coronary syndromes?

A. Ariza-Solé, Á. Cequier, J. Salazar-Mendiguchía, 2014, International journal of cardiology.

Dilated Cardiomyopathy and Hydroxychloroquine-induced Phospholipidosis: From Curvilinear Bodies to Clinical Suspicion.

Á. Cequier, J. Salazar-Mendiguchía, M. Olivé, 2017, Revista espanola de cardiologia.

Clinical Profile of Cardiac Involvement in Danon Disease

J. Mogensen, J. Kaski, L. Monserrat, 2020, Circulation. Genomic and precision medicine.

Clinical Findings and Prognosis of Danon Disease. An Analysis of the Spanish Multicenter Danon Registry.

R. Brugada, P. García-Pavía, J. Salazar-Mendiguchía, 2019, Revista espanola de cardiologia.

Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy

P. Elliott, L. Monserrat, P. Syrris, 2020, Heart.

Long-term Follow-up of Symptomatic Adult Patients With Noncompaction Cardiomyopathy.

J. Lupón, J. Salazar-Mendiguchía, J. González-Costello, 2017, Revista espanola de cardiologia.

The Cardiomyopathy Registry of the EURObservational Research Programme of the European Society of Cardiology: baseline data and contemporary management of adult patients with cardiomyopathies

L. Tavazzi, J. Čelutkienė, P. Seferovic, 2018, European heart journal.

Genotype–phenotype correlation of LMNA variants involving the Arg541 residue: a case report with multimodality imaging and literature review

J. Salazar-Mendiguchía, I. Anguera, A. Di Marco, 2020, ESC heart failure.

Clinical presentations of hypertrophic cardiomyopathy and implications for therapy

J. Salazar-Mendiguchía, C. Díez-López, Joel Salazar-Mendiguchía, 2018, Global cardiology science & practice.

Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach

J. Brugada, R. Brugada, S. César, 2021, Journal of personalized medicine.

Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease

P. Noseworthy, B. Gersh, E. González-López, 2016 .

Clinical Signi ﬁ cance and Potential Mechanism of Discordance Between Apolipoprotein and

E. González-López, P. García-Pavía, J. Salazar-Mendiguchía, 2016 .

Prediction of bleeding in patients with acute coronary syndromes: applying the new BARC definition.

A. Ariza-Solé, Á. Cequier, J. Ferreiro, 2014, Thrombosis research.

Familial evaluation reveals a distinct genetic cause in a large Spanish family with neurofibromatosis 1 and hypertrophic cardiomyopathy.

L. Monserrat, S. César, J. Salazar-Mendiguchía, 2020, Gene.

An unusual complication of a Takotsubo cardiomyopathy: a not so benign disease?

Á. Cequier, J. Salazar-Mendiguchía, V. Lorente, 2011, International journal of cardiology.

Coronary Embolization in Hypertrophic Cardiomyopathy With Left Ventricular Apical Aneurysm. Does Follow-Up With Cardiac Magnetic Resonance Have a Role?

Á. Cequier, J. Salazar-Mendiguchía, E. Claver, 2015, The American journal of cardiology.

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.

P. Elliott, J. Mogensen, L. Monserrat, 2018, Journal of the American College of Cardiology.

Direct oral anticoagulants in patients with hypertrophic cardiomyopathy and atrial fibrillation.

F. Domínguez, P. García-Pavía, T. Ripoll-Vera, 2017, International journal of cardiology.

Invasive mechanical ventilation in acute coronary syndromes in the era of percutaneous coronary intervention

J. Salazar-Mendiguchía, J. González-Costello, J. Sánchez-Salado, 2013, European heart journal. Acute cardiovascular care.

Management of myocardial infarction in the elderly. Insights from Spanish Minimum Basic Data Set

José Luis Bernal, A. Íñiguez, A. Ariza-Solé, 2019, European heart journal. Acute cardiovascular care.

Predictive ability of bleeding risk scores in the routine clinical practice

A. Ariza-Solé, Á. Cequier, J. Ferreiro, 2015, European heart journal. Acute cardiovascular care.

CRUSADE bleeding risk score validation for ST-segment-elevation myocardial infarction undergoing primary percutaneous coronary intervention.

A. Ariza-Solé, J. Salazar-Mendiguchía, J. Sánchez-Salado, 2013, Thrombosis research.

Body mass index and acute coronary syndromes: Paradox or confusion?

A. Ariza-Solé, Á. Cequier, J. Ferreiro, 2015, European heart journal. Acute cardiovascular care.

Current HHT genetic overview in Spain and its phenotypic correlation: data from RiHHTa registry

M. L. Pérez, J. Salazar-Mendiguchía, A. Riera-Mestre, 2020, Orphanet Journal of Rare Diseases.

Renal function improvement after conversion to proliferation signal inhibitors during long-term follow-up in heart transplant recipients.

Á. Cequier, J. Salazar-Mendiguchía, J. González-Costello, 2012, Transplantation proceedings.

High Rate of Discontinuation of a Mammalian Target of Rapamycin Inhibitor-based Regime During Long-term Follow-up of Cardiac Transplant Recipients

Á. Cequier, J. Salazar-Mendiguchía, J. González-Costello, 2013 .

Anthracycline-mediated cardiomyopathy: basic molecular knowledge for the cardiologist.

A. Ariza-Solé, Á. Cequier, J. Salazar-Mendiguchía, 2014, Archivos de cardiologia de Mexico.

Psychiatric and cognitive characteristics of individuals with Danon disease (LAMP2 gene mutation)

H. Mandel, P. García-Pavía, G. Quarta, 2017, American journal of medical genetics. Part A.

Prognosis of elderly ST-segment elevation myocardial infarction patients undergoing primary percutaneous coronary intervention.

A. Ariza-Solé, F. Formiga, J. Salazar-Mendiguchía, 2014, American heart journal.

Healthcare resources and costs associated with nonvalvular atrial fibrillation in Spain: apixaban versus acenocoumarol

J. Salazar-Mendiguchía, J. C. Colet, A. Mainar, 2023, Journal of comparative effectiveness research.

Does anemia affect the predictive ability of bleeding risk scores in patients with acute coronary syndromes?

A. Ariza-Solé, A. Garay, Á. Cequier, 2016, Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology.

Impact of anaemia on mortality and its causes in elderly patients with acute coronary syndromes.

A. Ariza-Solé, A. Garay, Á. Cequier, 2015, Heart, lung & circulation.

Hydroxychloroquine Myocardial Toxicity in a Patient with Systemic Lupus Erythematosus

J. Salazar-Mendiguchía, X. Corbella, M. Rubio-Rivas, 2015 .

Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease.

E. González-López, B. Bornstein, P. García-Pavía, 2016, Journal of the American College of Cardiology.