Lista de obras - Lorenzo Monserrat - Dominio Público Uruguay

A family with recurrent sudden death and no clinical clue.

artículo científico publicado en 2012

A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy.

artículo científico publicado en 2014

A new simple method to assess global left ventricular systolic function based on the sum of regional myocardial velocities

artículo científico publicado en 2005

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD).

artículo científico publicado en 2013

Accuracy of exercise echocardiography to detect coronary artery disease in left bundle branch block unassociated with either acute or healed myocardial infarction

artículo científico publicado en 2000

Accuracy of peak treadmill exercise echocardiography to detect multivessel coronary artery disease: comparison with post-exercise echocardiography

scientific article published on 01 September 2003

Apical hypertrophic cardiomyopathy and left ventricular non-compaction: two faces of the same disease

artículo científico publicado en 2008

Atlas of the clinical genetics of human dilated cardiomyopathy

artículo científico publicado en 2015

Cardiac challenges in patients with Fabry disease

artículo científico publicado en 2009

Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy

artículo científico publicado en 2010

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases

artículo científico publicado en 2007

Comments on the ESC guidelines on the management of cardiovascular diseases during pregnancy. A critical vision of Spanish cardiology

artículo científico publicado en 2012

Comparison of 2- and 3-dimensional exercise echocardiography for the detection of coronary artery disease.

artículo científico publicado en 2007

Comparison of exercise echocardiography to exercise electrocardiographic testing added to echocardiography at rest for risk stratification after uncomplicated acute myocardial infarction

artículo científico publicado en 2003

Comparison of peak and postexercise treadmill echocardiography with the use of continuous harmonic imaging acquisition

artículo científico publicado en 2004

Cytomegalovirus colitis mimicking a colonic neoplasm or ischemic colitis 4 years after heart transplantation

artículo científico publicado en 1998

Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype.

artículo científico publicado en 2014

Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study)

artículo científico publicado en 2015

Diagnostic Yield of Genetic Testing in Young Athletes With T-Wave Inversion

artículo científico publicado en 2018

Effect of crossbreeding with Limousine, Rubia Gallega and Belgium Blue on meat quality and fatty acid profile of Holstein calves.

artículo científico publicado en 2015

Effects of weaning and finishing feeding treatment on fatty acids, especially cis and trans C18:1 isomers, in the Longissimus thoracis muscle of Galician Blond calves

artículo científico publicado en 2011

Exercise echocardiography and cardiac magnetic resonance imaging to predict outcome in patients with hypertrophic cardiomyopathy

artículo científico publicado en 2014

Exercise echocardiography with addition of atropine

artículo científico publicado en 2004

Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.

artículo científico publicado en 2004

Gene mutations in apical hypertrophic cardiomyopathy

artículo científico publicado en 2005

Genetic basis of familial dilated cardiomyopathy patients undergoing heart transplantation

artículo científico publicado en 2016

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

artículo científico publicado en 2010

Hypertrophic cardiomyopathy. A study of the troponin-T gene in 127 Spanish families

scientific article published on 01 December 2009

Insights into genotype-phenotype correlation in hypertrophic cardiomyopathy. Findings from 18 Spanish families with a single mutation in MYBPC3

artículo científico publicado en 2010

Interpretation of electrocardiographic abnormalities in hypertrophic cardiomyopathy with cardiac magnetic resonance

scientific article published on 14 June 2006

Large scale analysis of HCM mutations in sudden cardiac death

Left ventricular asynchrony in patients with hypertrophic cardiomyopathy: its determinants and its relation to left ventricular function.

artículo científico publicado en 2007

Left ventricular hypertrophy in Fabry disease: a practical approach to diagnosis

artículo científico publicado en 2012

MRI of subendocardial perfusion deficits in isolated left ventricular noncompaction

artículo científico publicado en 2002

Magnetic resonance imaging of delayed enhancement in hypertrophic cardiomyopathy: relationship with left ventricular perfusion and contractile function

artículo científico publicado en 2006

Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic

artículo científico publicado en 2014

Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects

artículo científico publicado en 2007

Mutational screening of phospholamban gene in hypertrophic and idiopathic dilated cardiomyopathy and functional study of the PLN -42 C>G mutation.

artículo científico publicado en 2006

Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy

artículo científico publicado en 2013

Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: an independent marker of sudden death risk in young patients

scientific article published on 01 September 2003

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

artículo científico publicado en 2014

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?

artículo científico publicado en 2010

Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain

artículo científico publicado en 2015

Prediction of thrombo-embolic risk in patients with hypertrophic cardiomyopathy (HCM Risk-CVA).

artículo científico publicado en 2015

Prevalence of fabry disease in a cohort of 508 unrelated patients with hypertrophic cardiomyopathy

artículo científico publicado en 2007

Prognostic value of exercise echocardiography in patients with hypertrophic cardiomyopathy

artículo científico publicado en 2011

Relation of Left Ventricular Chamber Stiffness at Rest to Exercise Capacity in Hypertrophic Cardiomyopathy

artículo científico publicado en 2007

Response by Sheikh et al to Letter Regarding Article, "Diagnostic Yield of Genetic Testing in Young Athletes With T-Wave Inversion"

scientific article published on 01 February 2019

Risk stratification by treadmill exercise echocardiography

artículo científico publicado en 2006

Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy

artículo científico publicado en 2010

Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy

artículo científico publicado en 2013

Standard mutation nomenclature in hypertrophic cardiomyopathy: an urgent need

artículo científico publicado en 2005

Sudden death in a patient with lamin A/C gene mutation and near normal left ventricular systolic function

artículo científico publicado en 2007

Sudden death in hypertrophic cardiomyopathy: identification of high risk patients.

artículo científico publicado en 2000

The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans

artículo científico publicado en 2010

Usefulness of genetic diagnosis in a woman with hypertrophic cardiomyopathy and the desire for motherhood: information is key

artículo científico publicado en 2014

Valor pronóstico de la ecocardiografía de ejercicio en cinta rodante

artículo científico publicado en 2005

Valor pronóstico de la regurgitación mitral en reposo y ejercicio durante la ecocardiografía de ejercicio en pacientes con disfunción ventricular izquierda

artículo científico publicado en 2007

[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy]

artículo científico publicado en 2006

[Clinical significance of late gadolinium enhancement on cardiovascular magnetic resonance in patients with hypertrophic cardiomyopathy]

scientific article published on 01 January 2007

[Left ventricular noncompaction: a disease in search of a definition]

scientific article published on 01 February 2008

[The implantable cardioverter-defibrillator and hypertrophic cardiomyopathy. Experience at three centers].

artículo científico publicado en 2006

[Update on clinical cardiology: aortic diseases, hypertrophic cardiomyopathy, and prophylaxis of infective endocarditis]

artículo científico publicado en 2009

p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient

scientific journal article

Lista de obras de Lorenzo Monserrat

A family with recurrent sudden death and no clinical clue.

A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy.

A new simple method to assess global left ventricular systolic function based on the sum of regional myocardial velocities

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD).

Accuracy of exercise echocardiography to detect coronary artery disease in left bundle branch block unassociated with either acute or healed myocardial infarction

Accuracy of peak treadmill exercise echocardiography to detect multivessel coronary artery disease: comparison with post-exercise echocardiography

Apical hypertrophic cardiomyopathy and left ventricular non-compaction: two faces of the same disease

Atlas of the clinical genetics of human dilated cardiomyopathy

Cardiac challenges in patients with Fabry disease

Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases

Comments on the ESC guidelines on the management of cardiovascular diseases during pregnancy. A critical vision of Spanish cardiology

Comparison of 2- and 3-dimensional exercise echocardiography for the detection of coronary artery disease.

Comparison of exercise echocardiography to exercise electrocardiographic testing added to echocardiography at rest for risk stratification after uncomplicated acute myocardial infarction

Comparison of peak and postexercise treadmill echocardiography with the use of continuous harmonic imaging acquisition

Cytomegalovirus colitis mimicking a colonic neoplasm or ischemic colitis 4 years after heart transplantation

Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype.

Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study)

Diagnostic Yield of Genetic Testing in Young Athletes With T-Wave Inversion

Effect of crossbreeding with Limousine, Rubia Gallega and Belgium Blue on meat quality and fatty acid profile of Holstein calves.

Effects of weaning and finishing feeding treatment on fatty acids, especially cis and trans C18:1 isomers, in the Longissimus thoracis muscle of Galician Blond calves

Exercise echocardiography and cardiac magnetic resonance imaging to predict outcome in patients with hypertrophic cardiomyopathy

Exercise echocardiography with addition of atropine

Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.

Gene mutations in apical hypertrophic cardiomyopathy

Genetic basis of familial dilated cardiomyopathy patients undergoing heart transplantation

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

Hypertrophic cardiomyopathy. A study of the troponin-T gene in 127 Spanish families

Insights into genotype-phenotype correlation in hypertrophic cardiomyopathy. Findings from 18 Spanish families with a single mutation in MYBPC3

Interpretation of electrocardiographic abnormalities in hypertrophic cardiomyopathy with cardiac magnetic resonance

Large scale analysis of HCM mutations in sudden cardiac death

Left ventricular asynchrony in patients with hypertrophic cardiomyopathy: its determinants and its relation to left ventricular function.

Left ventricular hypertrophy in Fabry disease: a practical approach to diagnosis

MRI of subendocardial perfusion deficits in isolated left ventricular noncompaction

Magnetic resonance imaging of delayed enhancement in hypertrophic cardiomyopathy: relationship with left ventricular perfusion and contractile function

Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic

Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects

Mutational screening of phospholamban gene in hypertrophic and idiopathic dilated cardiomyopathy and functional study of the PLN -42 C>G mutation.

Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy

Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: an independent marker of sudden death risk in young patients

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?

Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain

Prediction of thrombo-embolic risk in patients with hypertrophic cardiomyopathy (HCM Risk-CVA).

Prevalence of fabry disease in a cohort of 508 unrelated patients with hypertrophic cardiomyopathy

Prognostic value of exercise echocardiography in patients with hypertrophic cardiomyopathy

Relation of Left Ventricular Chamber Stiffness at Rest to Exercise Capacity in Hypertrophic Cardiomyopathy

Response by Sheikh et al to Letter Regarding Article, "Diagnostic Yield of Genetic Testing in Young Athletes With T-Wave Inversion"

Risk stratification by treadmill exercise echocardiography

Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy

Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy

Standard mutation nomenclature in hypertrophic cardiomyopathy: an urgent need

Sudden death in a patient with lamin A/C gene mutation and near normal left ventricular systolic function

Sudden death in hypertrophic cardiomyopathy: identification of high risk patients.

The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans

Usefulness of genetic diagnosis in a woman with hypertrophic cardiomyopathy and the desire for motherhood: information is key

Valor pronóstico de la ecocardiografía de ejercicio en cinta rodante

Valor pronóstico de la regurgitación mitral en reposo y ejercicio durante la ecocardiografía de ejercicio en pacientes con disfunción ventricular izquierda

[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy]

[Clinical significance of late gadolinium enhancement on cardiovascular magnetic resonance in patients with hypertrophic cardiomyopathy]

[Left ventricular noncompaction: a disease in search of a definition]

[The implantable cardioverter-defibrillator and hypertrophic cardiomyopathy. Experience at three centers].

[Update on clinical cardiology: aortic diseases, hypertrophic cardiomyopathy, and prophylaxis of infective endocarditis]

p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient