María Martín

发表

Real Structural Valve Deterioration of the Mitroflow Aortic Prosthesis: Competing Risk Analysis.

V. León, R. Del Valle, V. Barriales, 2017, Revista espanola de cardiologia.

Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 Genes in the Risk of Atherosclerosis and Myocardial Infarction

V. Álvarez, E. Coto, V. Andrés, 2007, Cell cycle.

The APOB polymorphism rs1801701 A/G (p.R3638Q) is an independent risk factor for early-onset coronary artery disease: Data from a Spanish cohort.

E. Coto, C. Díaz-Corte, P. Avanzas, 2021, Nutrition, metabolism, and cardiovascular diseases : NMCD.

IL17RA in early-onset coronary artery disease: Total leukocyte transcript analysis and promoter polymorphism (rs4819554) association.

E. Coto, C. Díaz-Corte, P. Avanzas, 2020, Cytokine.

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease.

E. Coto, C. Díaz-Corte, P. Avanzas, 2019, Immunology letters.

Non compaction cardiomyopathy: Review of a controversial entity.

María Martín, R. Lorca, J. Rozado, 2018, Medicina clinica.

Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy.

V. Álvarez, E. Coto, María Martín, 2012, The Journal of molecular diagnostics : JMD.

Importance of definition and technique when using noninvasive coronary angiography to diagnose myocardial bridging.

A. Renilla, J. M. de la Hera, María Martín, 2013, Revista espanola de cardiologia.

Relevance of Etiological Study of Aortic Dissection: Family History and Histology as Key Players.

María Martín, C. Morís, Marcel Alméndarez, 2017, Revista espanola de cardiologia.

Metalloproteinase polymorphisms and bicuspid aortic valves.

E. Coto, María Martín, I. Rodríguez, 2010, Revista espanola de cardiologia.

Transcatheter Aortic Valve Implantation and Subclinical and Clinical Leaflet Thrombosis: Multimodality Imaging for Diagnosis and Risk Stratification

J. Cuevas, María Martín, C. Morís, 2021, European cardiology.

[Aortic valve replacement in octogenarians with severe aortic stenosis. Experience in a series of consecutive patients at a single center].

D. Calvo, P. Avanzas, I. Lozano, 2007, Revista espanola de cardiologia.

Response to Survivors of Aortic Dissection: Activity, Mental Health, and Sexual Function; and Exercise and Physical Activity for the Post–Aortic Dissection Patient: The Clinician's Conundrum

J. M. de la Hera, María Martín, C. Morís, 2016, Clinical cardiology.

Self-expanding transcatheter aortic valve implantation for degenerated Mitroflow bioprosthesis: Early outcomes.

F. Alfonso, V. León, R. Del Valle, 2019, International journal of cardiology.

Comparing American, European and Asian practice guidelines for aortic diseases.

D. Hernández-Vaquero, I. Pascual, María Martín, 2017, Journal of thoracic disease.

Nonsyndromic thoracic aortic aneurysm and dissection: Finally answers.

V. Barriales, María Martín, C. Morís, 2016, International journal of cardiology.

Profile of microRNAs differentially produced in hearts from patients with hypertrophic cardiomyopathy and sarcomeric mutations.

V. Álvarez, E. Coto, María Martín, 2011, Clinical chemistry.

Hypertrophic cardiomyopathy and left ventricular non-compaction: Different manifestations of the same cardiomyopathy spectrum?

E. Coto, María Martín, C. Morís, 2015, International journal of cardiology.

Vascular approaches for transcatheter aortic valve implantation.

A. Carro, P. Avanzas, R. Diaz, 2017, Journal of thoracic disease.

Atrial septal dissection and left-to-right shunt after mitral valve replacement: assessment with real-time three-dimensional transoesophageal echocardiography.

C. Corros, A. García-Campos, J. M. de la Hera, 2014, European heart journal cardiovascular Imaging.

Characterization of Left Ventricular Non-Compaction Cardiomyopathy

E. Coto, A. Astudillo, P. Avanzas, 2020, Journal of clinical medicine.

Late gadolinium enhancement in non-compaction cardiomyopathy.

María Martín, C. Morís, A. Saiz, 2009, Revista espanola de cardiologia.

Appropriate criteria for the use of cardiac computed tomography angiography.

C. Corros, A. García-Campos, J. M. de la Hera, 2013, European heart journal cardiovascular Imaging.

Left ventricle non-compaction: The still misdiagnosed cardiomyopathy.

A. Astudillo, María Martín, C. Morís, 2016, International journal of cardiology.

Thoracic Aneurysms and Dissections: Towards a Further and Better Knowledge

María Martín, C. Morís, J. Rozado, 2017, Journal of Cardiovascular Translational Research.

Left ventricle non-compaction cardiomyopathy: different clinical scenarios and magnetic resonance imaging findings.

C. Corros, A. García-Campos, V. Barriales, 2013, Archivos de cardiologia de Mexico.

IL6 gene polymorphism association with calcific aortic valve stenosis and influence on serum levels of interleukin-6

María Martín, C. Morís, I. Rodríguez, 2022, Frontiers in Cardiovascular Medicine.

Insights Into Hypertrophic Cardiomyopathy Evaluation Through Follow-up of a Founder Pathogenic Variant.

E. Coto, V. León, I. Pascual, 2019, Revista espanola de cardiologia.

Primary cardiac tumors: 32 years of experience from a Spanish tertiary surgical center.

A. Renilla, V. Barriales, María Martín, 2013, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

Usefulness of cardiac MRI in the early diagnosis of endomyocardial fibrosis.

C. Corros, María Martín, J. L. Lambert, 2012, Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology.

Athlete's heart and other entities to consider around

María Martín, A. Adeba, 2020, Clinical cardiology.

The importance of echocardiography in Transcatheter Aortic Valve Implantation

C. Corros, P. Avanzas, María Martín, 2014, Echocardiography.

Turner syndrome, unicuspid aortopathy, and pregnancy: Difficult decisions for complex scenarios

J. M. de la Hera, María Martín, Helena Cigarrán, 2021, Archivos de cardiologia de Mexico.

Turner syndrome and pregnancy: A multidisciplinary approach.

María Martín, Mária Luisa Rodríguez, R. Alvarez, 2018, Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology.

Young male with long-term impaired ejection fraction - endocardial fibroelastosis: The importance of cardiac magnetic resonance.

María Martín, C. Morís, A. Alperi, 2019, Archivos de cardiologia de Mexico.

TGFBR2 gene mutational spectrum in aortic pathology.

E. Coto, María Martín, I. Rodríguez, 2011, Journal of the American College of Cardiology.

Usefulness of cardiac magnetic resonance imaging in left ventricular non‐compaction cardiomyopathy

C. Corros, V. Barriales, María Martín, 2011, European journal of heart failure.

The Prevalence of Patient-Prosthesis Mismatch Can Be Reduced Using the Trifecta Aortic Prosthesis.

D. Calvo, V. León, P. Avanzas, 2018, The Annals of thoracic surgery.

State anxiety and trait anxiety in patients with aortic pathology. Another therapeutic target?

María Martín, C. Morís, A. Alperi, 2021, Revista de psiquiatria y salud mental.

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor next-generation sequencing.

V. Álvarez, E. Coto, María Martín, 2014, Circulation journal : official journal of the Japanese Circulation Society.

Variants in cardiac GATA genes associated with bicuspid aortic valve

E. Coto, J. Cannata-Andía, María Martín, 2018, European journal of clinical investigation.

Evaluation of cardiovascular events in patients with hepatocellular carcinoma treated with sorafenib in the clinical practice. The CARDIO‐SOR study

M. Varela, A. Castaño-García, María Martín, 2021, Liver international (Print).

Correlation of Micro-Computed Tomography Assessment of Valvular Mineralisation with Histopathological and Immunohistochemical Features of Calcific Aortic Valve Disease

J. Valdivielso, María Martín, C. Morís, 2019, Journal of clinical medicine.

Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients

V. Álvarez, E. Coto, P. Avanzas, 2017, Circulation. Cardiovascular genetics.

Sinus of Valsalva fistula to right chambers: an infrequent pathology.

C. Corros, J. M. de la Hera, María Martín, 2014, Hellenic Journal of Cardiology.

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

X. Puente, R. Valdés-Mas, Diana A. Puente, 2014, Nature Communications.

Uncommon giant circumflex coronary artery fistula.

María Martín, A. Súarez, Helena Cigarrán, 2020, Kardiologia polska.

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy.

E. Coto, P. Avanzas, María Martín, 2018, Epigenomics.

Update in Biomolecular and Genetic Bases of Bicuspid Aortopathy

María Martín, I. Rodríguez, Alejandro Junco-Vicente, 2021, International journal of molecular sciences.

[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy].

V. Álvarez, E. Coto, M. García-Castro, 2009, Revista espanola de cardiologia.

DNA variation in myoMIRs of the 1, 133, and 208 families in hypertrophic cardiomyopathy

V. Álvarez, E. Coto, María Martín, 2011 .

Open Access RESEARCH

V. Álvarez, E. Coto, R. Tarnawski, 2010 .

Takotsubo syndrome after heart valve surgery.

C. Corros, María Martín, C. Morís, 2015, International journal of cardiology.

Pregnancy in aortopathies: Foresight and anticipation.

V. Barriales, María Martín, C. Morís, 2016, International journal of cardiology.

Type A Aortic Dissection: The Controversy of the Root Replacement.

A. García-Campos, María Martín, C. Morís, 2015, The Annals of thoracic surgery.

Bicuspid aortic valve syndrome: a heterogeneous and still unknown condition.

María Martín, C. Morís, I. Rodríguez, 2014, International journal of cardiology.

Severe Intramyocardial Hematoma as a Complication of Retrograde Approach in Chronic Total Occlusion.

C. Corros, P. Avanzas, D. Hernández-Vaquero, 2017, JACC. Cardiovascular interventions.

Bicuspid aortic valve syndrome: a multidisciplinary approach for a complex entity.

I. Pascual, María Martín, C. Morís, 2017, Journal of thoracic disease.

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain).

V. Álvarez, E. Coto, María Martín, 2013, International journal of cardiology.

5-Hydroxytryptamine 5-HT2A receptor and 5-hydroxytryptamine transporter polymorphisms in acute myocardial infarction.

V. Álvarez, E. Coto, A. Batalla, 2003, Clinical science.

Real incidence of diabetes mellitus in a coronary disease population.

E. Delgado, J. M. García-Ruíz, P. Martínez-Camblor, 2013, The American journal of cardiology.

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.

V. Álvarez, E. Coto, A. Batalla, 2011, Mitochondrion.

Supravalvular aortic stenosis as a non-syndromic familial disease. Relevance of familial screening.

J. M. García-Ruíz, C. Corros, A. García-Campos, 2014, International journal of cardiology.

Low transcriptional activity haplotype of matrix metalloproteinase 1 is less frequent in bicuspid aortic valve patients.

J. Cannata-Andía, María Martín, C. Morís, 2013, Gene.

Rare genetic variants in GATA transcription factors in patients with hypertrophic cardiomyopathy

E. Coto, J. Cannata-Andía, María Martín, 2017, Journal of Investigative Medicine.

An incidental finding during cardiac catheterization.

P. Avanzas, María Martín, C. Morís, 2006, International Journal of Cardiology.

Aortic stenosis: a complex, atherosclerosis-like, multifactorial disease.

J. Cannata-Andía, María Martín, I. Rodríguez, 2013, International journal of cardiology.

Diagnostic impact of genetic testing in hypertrophic cardiomyopathy: The story of two families.

E. Coto, María Martín, C. Morís, 2016, International journal of cardiology.

Usefulness of coronary computed tomography angiography in asymptomatic patients.

A. Renilla, María Martín, M. Barreiro, 2013, Revista espanola de cardiologia.

Subclinical leaflet thrombosis after TAVI: To be or not to be.

María Martín, C. Morís, 2023, International Journal of Cardiology.

Miocardiopatía no compactada: una miocardiopatía con controversias

María Martín, R. Lorca, J. Rozado, 2017 .

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.

V. Álvarez, E. Coto, A. Batalla, 2011, Mitochondrion.

Diagnostic impact of genetic testing in hypertrophic cardiomyopathy: The story of two families.

E. Coto, María Martín, C. Morís, 2016, International journal of cardiology.

Usefulness of coronary computed tomography angiography in asymptomatic patients.

A. Renilla, María Martín, M. Barreiro, 2013, Revista espanola de cardiologia.

Bicuspid aortic valve aortopathy syndrome: a potentially familiar disease.

María Martín, I. Rodríguez, I. A. Pichel, 2013, The American journal of medicine.

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

X. Puente, R. Valdés-Mas, Diana A. Puente, 2014, Nature Communications.

Pregnancy and Cardiac Disease: Making Headway.

María Martín, C. Morís, J. J. Rodríguez Reguero, 2017, Revista espanola de cardiologia.

Biscuspid aortic valve syndrome: diversity and controversy

V. Barriales, María Martín, C. Morís, 2016, The International Journal of Cardiovascular Imaging.