Search Results - "Pasotti, Michele"
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Prognostic Relevance of Pulmonary Arterial Compliance in Patients With Chronic Heart Failure
Published in Chest (01-05-2014)“…Background Reduced pulmonary arterial compliance (Ca) is a marker of poor prognosis in idiopathic pulmonary arterial hypertension. We tested the hypothesis…”
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Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies
Published in Journal of the American College of Cardiology (07-10-2008)“…Objectives The aim of this study was to analyze the long-term follow-up of dilated cardiolaminopathies. Background Lamin A/C ( LMNA ) gene mutations cause a…”
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The MOGE(S) Classification for a Phenotype-Genotype Nomenclature of Cardiomyopathy
Published in Journal of the American College of Cardiology (17-06-2014)“…[...]I hope that this new classification will open the doors to the unresolved problem of phenotype-genotype correlation, considering first of all families…”
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Diagnostic Work-Up and Risk Stratification in X-Linked Dilated Cardiomyopathies Caused by Dystrophin Defects
Published in Journal of the American College of Cardiology (23-08-2011)“…Objectives We sought to describe the diagnostic work-up, phenotype, and long-term evolution of dilated cardiomyopathy (DCM) associated with Dystrophin (DYS)…”
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Effects of n-3 polyunsaturated fatty acids and of rosuvastatin on left ventricular function in chronic heart failure: a substudy of GISSI-HF trial
Published in European journal of heart failure (01-12-2010)“…Aims The GISSI‐HF trial showed that n‐3 polyunsaturated fatty acids (PUFA), but not rosuvastatin, reduce morbidity and mortality in patients with symptomatic…”
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A rare case of discrete aortic coarctation in Williams-Beuren syndrome. Diagnostic and therapeutic considerations
Published in La Pediatria medica e chirurgica (29-09-2015)“…Williams-Beuren syndrome (WBS) is a genetic disorder caused by elastin gene deletions, and is characterized by cardiovascular malformations, primarily…”
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Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers
Published in Journal of the American College of Cardiology (01-01-2012)“…Objectives The purpose of this study was to determine risk factors that predict malignant ventricular arrhythmias (MVA) in Lamin A/C ( LMNA ) mutation…”
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Coronary atherosclerosis in end-stage idiopathic dilated cardiomyopathy: an innocent bystander?
Published in European heart journal (01-08-2005)“…Aims Coronary atherosclerosis is occasionally found in the hearts of patients diagnosed with idiopathic dilated cardiomyopathy (IDCM), who have undergone heart…”
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Prognostic relevance of the echocardiographic assessment of right ventricular function in patients with idiopathic pulmonary arterial hypertension
Published in International journal of cardiology (30-04-2010)“…Abstract Background In patients with idiopathic pulmonary hypertension (IPAH) progression of the disease and survival are related to the capability of the…”
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Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers: A European Cohort Study
Published in Journal of the American College of Cardiology (31-01-2012)“…The purpose of this study was to determine risk factors that predict malignant ventricular arrhythmias (MVA) in Lamin A/C (LMNA) mutation carriers. LMNA…”
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Long-term left ventricular reverse remodelling with cardiac resynchronization therapy: results from the CARE-HF trial
Published in European journal of heart failure (01-05-2009)“…Aims The aim of the present study was to assess the long-term effects of cardiac resynchronization therapy (CRT) on the reverse remodelling of the left…”
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Impediments to Heart Transplantation in Adults With MELAS:m.3243A>G Cardiomyopathy
Published in Journal of the American College of Cardiology (01-10-2022)Get full text
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Usefulness of cardiac magnetic resonance in assessing the risk of ventricular arrhythmias and sudden death in patients with hypertrophic cardiomyopathy
Published in European heart journal (01-08-2009)“…Aims To assess the relationship between cardiovascular magnetic resonance (CMR) parameters and both spontaneous ventricular tachycardia (VT) and risk of sudden…”
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Desmin accumulation restrictive cardiomyopathy and atrioventricular block associated with desmin gene defects
Published in European journal of heart failure (01-08-2006)“…Abstract Background Primary desminopathies are caused by desmin gene [DES (MIM*125660)] mutations. The clinical spectrum includes pure myopathies,…”
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Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2)
Published in Heart (British Cardiac Society) (01-02-2011)“…To evaluate the prevalence and phenotype of smooth muscle alpha-actin (ACTA2) mutations in non-syndromic thoracic aortic aneurysms and dissections (TAAD)…”
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Effect of a westward transmeridian flight on ambulatory blood pressure monitoring in normotensive subjects
Published in Journal of hypertension (01-02-1997)“…OBJECTIVETo evaluate the effects of a westward transmeridian flight over six time zones (from Milan to New York) on ambulatory blood pressure monitoring (ABPM)…”
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Impediments to Heart Transplantation in Adults With MELASMT-TL1:m.3243A>G Cardiomyopathy
Published in Journal of the American College of Cardiology (11-10-2022)“…BACKGROUNDThe heart is commonly involved in maternally inherited mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)…”
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The MOGE(S) Classification for a Phenotype-Genotype Nomenclature of Cardiomyopathy: More Questions Than Answers?
Published in Journal of the American College of Cardiology (17-06-2014)Get full text
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Regional abnormalities of myocardial deformation in patients with hypertrophic cardiomyopathy: correlations with delayed enhancement in cardiac magnetic resonance
Published in European journal of heart failure (01-10-2009)“…Aims Hypertrophic cardiomyopathy (HCM) is a genetic disease histologically characterized by a profound disarray of myocardial fibres and by local fibrosis. We…”
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