Search Results - "Tomas, Vera"
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Multidisciplinary approach in the management of hATTR
Published in European journal of clinical investigation (01-10-2020)Get full text
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Prognostic effects of cardiovascular rehabilitation: facts and myths
Published in Panminerva medica (01-06-2021)“…Since CR was introduced, studies have been carried out to discover the effect of CRHPs on cardiovascular morbidity and mortality and on heart-disease patients'…”
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ESC EORP Cardiomyopathy Registry: real‐life practice of genetic counselling and testing in adult cardiomyopathy patients
Published in ESC Heart Failure (01-10-2020)“…Aims Cardiomyopathies comprise a heterogeneous group of diseases, often of genetic origin. We assessed the current practice of genetic counselling and testing…”
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New Variant in Placophilin-2 Gene Causing Arrhythmogenic Myocardiopathy
Published in Genes (27-04-2022)“…Arrhythmogenic cardiomyopathy (ACM) is an inherited disease characterized by progressive fibroadipose replacement of cardiomyocytes. Its diagnosis is based on…”
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Comparison of 1-Year Outcome in Patients With Severe Aorta Stenosis Treated Conservatively or by Aortic Valve Replacement or by Percutaneous Transcatheter Aortic Valve Implantation (Data from a Multicenter Spanish Registry)
Published in The American journal of cardiology (15-07-2016)“…The factors that influence decision making in severe aortic stenosis (AS) are unknown. Our aim was to assess, in patients with severe AS, the determinants of…”
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Early diagnosis in patients with transthyretin familial amyloid polyneuropathy: A comparative study
Published in Medicina clinica (20-01-2017)“…Transthyretin-associated familial amyloid polyneuropathy (TTR-FAP) is a disease caused by the deposit of abnormal transthyretin on tissues, mainly nerves…”
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Response to ECG, February 2015
Published in Revista española de cardiología (English ed.) (01-03-2015)Get full text
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The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans
Published in International journal of cardiology (19-11-2010)“…Abstract Background The R820W mutation in the MYBPC3 gene has been associated with the development of hypertrophic cardiomyopathy (HCM) in rag-doll cats, but…”
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Uncommon complication of late perforation of the right atrium with active fixation atrial electrode
Published in Medicina Clínica Práctica (01-10-2024)Get full text
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Impact of SARS‐Cov‐2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registry
Published in ESC Heart Failure (01-08-2022)“…Aims To describe the natural history of SARS‐CoV‐2 infection in patients with hypertrophic cardiomyopathy (HCM) compared with a control group and to identify…”
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Plan of Action for Inherited Cardiovascular Diseases: Synthesis of Recommendations and Action Algorithms
Published in Revista española de cardiología (English ed.) (01-03-2016)“…The term inherited cardiovascular disease encompasses a group of cardiovascular diseases (cardiomyopathies, channelopathies, certain aortic diseases, and other…”
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Controversy regarding ACE inhibitors / ARBs in COVID-19
Published in Revista española de cardiologia (01-06-2020)Get full text
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Clinical and Prognostic Profiles of Cardiomyopathies Caused by Mutations in the Troponin T Gene
Published in Revista española de cardiología (English ed.) (01-02-2016)“…Mutations in the troponin T gene (TTNT2) have been associated in small studies with the development of hypertrophic cardiomyopathy characterized by a high risk…”
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Multifunctionality and diversity of livestock grazing systems for sustainable food systems throughout the world: Are there learning opportunities for Europe?
Published in Grass and forage science (01-12-2022)“…Throughout the world, livestock grazing systems (LGS) include, and provide livelihoods for, many rural populations. These LGS are represented in a wide variety…”
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Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker
Published in Orphanet journal of rare diseases (08-07-2019)“…Identification of Fabry disease (FD) in cardiac patients has been restricted so far to patients with left ventricular hypertrophy. Conduction problems are…”
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Diagnostic yield of the implantable loop recorder in octogenarians
Published in European geriatric medicine (01-02-2019)“…Background/objectives Syncope in octogenarians represents an important problem in terms of comorbidity, quality of life and substantial medical costs,…”
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Cardiac filaminopathies: lights and shadows in the phenotype associated with the FLNC gene
Published in Revista española de cardiología (English ed.) (01-05-2023)Get full text
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Occupational practice in patients with hereditary transthyretin amyloidosis, a qualitative study
Published in Orphanet journal of rare diseases (10-11-2023)“…Hereditary transthyretin amyloidosis (ATTRv) is a rare genetic disease that negatively affects patients' quality of life through the involvement of various…”
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Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction
Published in Journal of the American College of Cardiology (17-08-2021)“…Left ventricular noncompaction (LVNC) is a heterogeneous entity with uncertain prognosis. This study sought to develop and validate a prediction model of major…”
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