Search Results - "Tomberli, Alessia"
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Doctor-patient care relationship in genetic cardiomyopathies: An exploratory study on clinical consultations
Published in PloS one (05-08-2020)“…Background The present study aims to explore the setting of consultation and communication between physicians and patients affected by genetic…”
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2
Prevalence of anxiety and depression symptoms in a sample of outpatients with ATTR cardiac amyloidosis
Published in Frontiers in psychology (18-01-2023)“…Patients with ATTR cardiac amyloidosis (ATTR-CA) face rare disease that could negatively influence psychological well-being with consequences on the course of…”
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3
Arrhythmic Burden in Cardiac Amyloidosis: What We Know and What We Do Not
Published in Biomedicines (01-11-2022)“…Cardiac amyloidosis (CA), caused by the deposition of insoluble amyloid fibrils, impairs different cardiac structures, altering not only left ventricle (LV)…”
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4
Comprehensive Risk Management in Arrhythmogenic Cardiomyopathy Associated With Autosomal Dominant Carvajal Syndrome
Published in JACC. Case reports (01-06-2020)“…In a 37-year-old cardiac arrest survivor with autosomal dominant Carvajal syndrome and arrhythmogenic cardiomyopathy, a desmoplakin mutation was identified…”
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5
The evolving paradigm and current perception of hypertrophic cardiomyopathy: Implications for management
Published in Progress in cardiovascular diseases (01-09-2023)“…Recent evidence from imaging and genetic screening studies has clearly shown that hypertrophic cardiomyopathy (HCM) is more common than initially perceived,…”
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Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center
Published in Genetics in medicine (01-02-2019)“…Purpose Genetic testing in hypertrophic cardiomyopathy (HCM) has long relied on Sanger sequencing of sarcomeric genes. The advent of next-generation sequencing…”
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7
Sex-related differences in clinical presentation and all-cause mortality in patients with cardiac transthyretin amyloidosis and light chain amyloidosis
Published in International journal of cardiology (15-03-2022)“…We aimed to ascertain whether sex-related differences are relevant to clinical presentation, cardiac phenotype and all-cause mortality in different types of…”
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8
Prevalence, causes and predictors of cardiovascular hospitalization in patients with hypertrophic cardiomyopathy
Published in International journal of cardiology (01-11-2020)“…Despite numerous studies assessing the natural history of patients with hypertrophic cardiomyopathy (HCM), there is lack of data regarding the burden of…”
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9
Mavacamten, a Novel Therapeutic Strategy for Obstructive Hypertrophic Cardiomyopathy
Published in Current cardiology reports (01-07-2021)“…Purpose of review Pharmacological treatment options for hypertrophic cardiomyopathy (HCM) are currently limited and comprise non-disease specific therapies…”
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10
Early Diagnosis and Outcome in Patients With Wild-Type Transthyretin Cardiac Amyloidosis
Published in Mayo Clinic proceedings (01-08-2021)“…Whether diagnostic timing in transthyretin (TTR) cardiac amyloidosis (CA) predisposes patients to worse outcomes is unresolved. We aimed to describe the…”
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11
Incidence of stroke in patients with hypertrophic cardiomyopathy in stable sinus rhythm during long-term monitoring
Published in International journal of cardiology (15-06-2023)“…Patients with hypertrophic cardiomyopathy (HCM) are at increased risk of stroke, but the incidence and factors associated with cardioembolic events in HCM…”
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12
686 ASSOCIATION OF PREGNANCY WITH THE NATURAL HISTORY OF WOMEN DIAGNOSED WITH HYPERTROPHIC CARDIOMYOPATHY
Published in European heart journal supplements (15-12-2022)“…Abstract Background Hypertrophic Cardiomyopathy (HCM) is the most common genetic cardiomyopathy. However, few studies have systematically investigated the…”
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13
Safety and efficacy of ranolazine in hypertrophic cardiomyopathy: Real-world experience in a National Referral Center
Published in International journal of cardiology (01-01-2023)“…We assessed the efficacy and safety of ranolazine in real-world patients with hypertrophic cardiomyopathy (HCM). Ranolazine is an anti-anginal drug that…”
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14
Impact of pregnancy on the natural history of women with hypertrophic cardiomyopathy
Published in European journal of preventive cardiology (05-01-2024)“…Abstract Aims Whether pregnancy is a modifier of the long-term course and outcome of women with hypertrophic cardiomyopathy (HCM) is unknown. We assessed the…”
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15
Red flags for the diagnosis of cardiac amyloidosis: simple suggestions to raise suspicion and achieve earlier diagnosis
Published in Journal of cardiovascular medicine (Hagerstown, Md.) (01-08-2022)“…Cardiac amyloidosis is an infiltrative disease characterized by extracellular deposition of insoluble amyloid fibrils in the heart leading to organ…”
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16
Cardiac involvement in eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss syndrome): Prospective evaluation at a tertiary referral centre
Published in European journal of internal medicine (01-03-2021)“…Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis. Cardiac specific involvement (CSI) is caused by coronary artery vasculitis,…”
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Sacubitril/valsartan for the treatment of non‐obstructive hypertrophic cardiomyopathy: An open label randomized controlled trial (SILICOFCM)
Published in European journal of heart failure (01-06-2024)“…Aim Sacubitril/valsartan treatment reduces mortality and hospitalizations in heart failure with reduced ejection fraction but has limited application in…”
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18
Targeted Medical Therapies for Hypertrophic Cardiomyopathy
Published in Current cardiology reports (28-01-2020)“…Purpose of Review The management of hypertrophic cardiomyopathy (HCM) has changed considerably over the years, although molecular therapies targeting core…”
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19
Red flags for the diagnosis of cardiac amyloidosis: simple suggestions to raise suspicion and achieve earlier diagnosis
Published in Journal of cardiovascular medicine (Hagerstown, Md.) (21-07-2022)“…Cardiac amyloidosis is an infiltrative disease characterized by extracellular deposition of insoluble amyloid fibrils in the heart leading to organ…”
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20
Prognostic value of cardiopulmonary exercise testing in patients with transthyretin cardiac amyloidosis
Published in Internal and emergency medicine (01-03-2023)“…The aim of this study is to evaluate the prognostic value of cardiopulmonary testing (CPET) in a cohort of patients with transthyretin cardiac amyloidosis…”
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