The International Society for Heart and Lung Transplantation (ISHLT) guidelines for the care of heart transplant recipients

A Velleca, MA Shullo, K Dhital, E Azeka… - The Journal of Heart …, 2023 - jhltonline.org
Cochrane, Maria Crespo Leiro, Anne Dipchand, Brian Feingold, Kathleen Grady, Edward
Horn, Maryl Johnson, Donna Mancini, Sean Pinney, Heather Ross, Kari Wujcik, Andreas …

An expert consensus document on the management of cardiovascular manifestations of Fabry disease

A Linhart, DP Germain, I Olivotto… - European journal of …, 2020 - Wiley Online Library
Fabry disease (FD) is an X‐linked lysosomal storage disorder caused by pathogenic
variants in the α‐galactosidase A (GLA) gene that leads to reduced or undetectable α …

Dietary thiols: A potential supporting strategy against oxidative stress in heart failure and muscular damage during sports activity

M Brancaccio, C Mennitti, A Cesaro, F Fimiani… - International Journal of …, 2020 - mdpi.com
Moderate exercise combined with proper nutrition are considered protective factors against
cardiovascular disease and musculoskeletal disorders. However, physical activity is known …

Diagnosis and management of cardiovascular involvement in Fabry disease

M Rubino, E Monda, M Lioncino… - Heart Failure …, 2022 - heartfailure.theclinics.com
KEY POINTS Fabry disease is a multisystemic disease that can affect several organs,
resulting in cardiac, neurologic, ocular, cutaneous, and renal manifestations. Age at onset …

Next-generation sequencing gene panels in Inheritable cardiomyopathies and channelopathies: prevalence of pathogenic variants and variants of unknown …

C Mazzaccara, R Lombardi, B Mirra, F Barretta… - Biomolecules, 2022 - mdpi.com
The diffusion of next-generation sequencing (NGS)-based approaches allows for the
identification of pathogenic mutations of cardiomyopathies and channelopathies in more …

Prevalence and clinical significance of red flags in patients with hypertrophic cardiomyopathy

G Limongelli, E Monda, S Tramonte, F Gragnano… - International journal of …, 2020 - Elsevier
Introduction We sought to determine prevalence and predictive accuracy of clinical markers
(red flags, RF), known to be associated with specific systemic disease in a consecutive …

Laboratory medicine: Health evaluation in elite athletes

B Lombardo, V Izzo, D Terracciano… - Clinical Chemistry and …, 2019 - degruyter.com
The need to evaluate the health status of an athlete represents a crucial aim in preventive
and protective sports science in order to identify the best diagnostic strategy to improve …

Molecular epidemiology of mitochondrial cardiomyopathy: a search among mitochondrial and nuclear genes

C Mazzaccara, B Mirra, F Barretta, M Caiazza… - International Journal of …, 2021 - mdpi.com
Mitochondrial Cardiomyopathy (MCM) is a common manifestation of multi-organ
Mitochondrial Diseases (MDs), occasionally present in non-syndromic cases. Diagnosis of …

ECG in dilated cardiomyopathy: specific findings and long-term prognostic significance

M Merlo, D Zaffalon, D Stolfo, A Altinier… - Journal of …, 2019 - journals.lww.com
Objective The objective was to provide an exhaustive characterization of ECG features in a
large cohort of dilated cardiomyopathies (DCMs) and then investigate their possible …

Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome

B Lombardo, V D'Argenio, E Monda… - … Genetics & Genomic …, 2020 - Wiley Online Library
Background Syndromic dilated cardiomyopathy (DCM) includes a group of complex
disorders with a very heterogeneous genetic etiology, leading to delay in definitive …