Results 1 to 10 of about 311,710 (149)

Evolving trends in epidemiology and natural history of cardiac amyloidosis: 30-year experience from a tertiary referral center for cardiomyopathies

Frontiers in Cardiovascular Medicine, 2022
ObjectiveNatural history of cardiac amyloidosis (CA) is poorly understood. We aimed to examine the changing mortality of different types of CA over a 30-year period.Patients and methodsConsecutive patients included in the “Trieste CA Registry” from ...
Aldostefano Porcari, Valentina Allegro, Riccardo Saro, Guerino Giuseppe Varrà, Linda Pagura, Maddalena Rossi, Andrea Lalario, Francesca Longo, Renata Korcova, Matteo Dal Ferro, Andrea Perkan, Franca Dore, Rossana Bussani, Giovanni Maria De Sabbata, Francesco Zaja, Francesco Zaja, Marco Merlo, Gianfranco Sinagra   +17 more
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1p36 Deletion Syndrome and the Aorta: A Report of Three New Patients and a Literature Review

Journal of Cardiovascular Development and Disease, 2021
Background: Monosomy 1p36 syndrome is now considered the most common terminal deletion syndrome, with an estimated incidence of 1 in 5000. Cardiac involvement is well described in the literature mainly in terms of congenital heart defects (CHDs) and ...
Valentina Lodato, Valeria Orlando, Viola Alesi, Silvia Di Tommaso, Mario Bengala, Giovanni Parlapiano, Elisa Agnolucci, Marianna Cicenia, Federica Calì, Maria Cristina Digilio, Fabrizio Drago, Antonio Novelli, Anwar Baban   +12 more
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Sex differences in natural history of cardiovascular magnetic resonance‐ and biopsy‐proven lymphocytic myocarditis

ESC Heart Failure, 2022
Aims The role of sex in determining the profile and the outcomes of patients with myocarditis is largely unexplored. We evaluated the impact of sex as a modifier factor in the clinical characterization and natural history of patients with definite ...
Matteo Castrichini, Aldostefano Porcari, Chiara Baggio, Giulia Gagno, Davide Maione, Giulia Barbati, Kristen Medo, Luisa Mestroni, Marco Merlo, Gianfranco Sinagra   +9 more
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Cardiomyopathies in Children and Systemic Disorders When Is It Useful to Look beyond the Heart?

Journal of Cardiovascular Development and Disease, 2022
Cardiomyopathy (CMP) is a rare disease in the pediatric population, with a high risk of morbidity and mortality. The genetic etiology of CMPs in children is extremely heterogenous.
Valentina Lodato, Giovanni Parlapiano, Federica Calì, Massimo Stefano Silvetti, Rachele Adorisio, Michela Armando, May El Hachem, Antonino Romanzo, Carlo Dionisi-Vici, Maria Cristina Digilio, Antonio Novelli, Fabrizio Drago, Massimiliano Raponi, Anwar Baban   +13 more
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Cardiovascular Involvement in Pediatric Laminopathies. Report of Six Patients and Literature Revision

Frontiers in Pediatrics, 2020
Lamin A/C (LMNA) encodes for two nuclear intermediate filament proteins. Mutations in LMNA cause a highly heterogeneous group of diseases predominantly leading to muscular or cardiac disease, lipodystrophy syndromes, peripheral neuropathy, and ...
Anwar Baban, Marianna Cicenia, Monia Magliozzi, Maria Gnazzo, Nicoletta Cantarutti, Massimo Stefano Silvetti, Rachele Adorisio, Bruno Dallapiccola, Enrico Bertini, Antonio Novelli, Fabrizio Drago   +10 more
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Geno- and phenotypic characteristics and clinical outcomes of CACNA1C gene mutation associated Timothy syndrome, “cardiac only” Timothy syndrome and isolated long QT syndrome 8: A systematic review

Frontiers in Cardiovascular Medicine, 2022
BackgroundMutations in the CACNA1C gene–encoding for the major Ca2+ channel of the heart–may exhibit a variety of clinical manifestations. These include typical or atypical Timothy syndromes (TS) which are associated with multiple organ manifestations ...
János Borbás, Máté Vámos, Lidia Hategan, Lilla Hanák, Nelli Farkas, Zsolt Szakács, Zsolt Szakács, Dezső Csupor, Dezső Csupor, Bálint Tél, Péter Kupó, Péter Kupó, Beáta Csányi, Viktória Nagy, András Komócsi, Tamás Habon, Tamás Habon, Péter Hegyi, Péter Hegyi, Péter Hegyi, Róbert Sepp   +20 more
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Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children

Biomolecules, 2021
Neuromuscular disorders (NMDs) are highly heterogenous from both an etiological and clinical point of view. Their signs and symptoms are often multisystemic, with frequent cardiac involvement.
Anwar Baban, Valentina Lodato, Giovanni Parlapiano, Corrado di Mambro, Rachele Adorisio, Enrico Silvio Bertini, Carlo Dionisi-Vici, Fabrizio Drago, Diego Martinelli   +8 more
doaj   +1 more source

Tapering of biological treatment in autoinflammatory diseases: a scoping review

Pediatric Rheumatology Online Journal, 2022
Background Biological treatment and treat-to-target approaches guide the achievement of inactive disease and clinical remission in Autoinflammatory Diseases (AID).
Tatjana Welzel, Lea Oefelein, Marinka Twilt, Marc Pfister, Jasmin B. Kuemmerle-Deschner, Susanne M. Benseler   +5 more
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Meta-Analysis of Prevalence of Erectile Dysfunction in Mainland China: Evidence Based on Epidemiological Surveys

Sexual Medicine, 2017
Introduction: The epidemiologic characteristics of erectile dysfunction (ED) in mainland China remain incompletely understood. Aim: To evaluate the overall prevalence and determine the severity of ED in mainland China.
Wenying Wang, MD, PhD, Jingyuan Fan, MD, Guifeng Huang, MD, Xi Zhu, MD, PhD, Ye Tian, MD, PhD, Hua Tan, PhD, Li Su, MD, PhD   +6 more
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Vitronectin-based hydrogels recapitulate neuroblastoma growth conditions

Frontiers in Cell and Developmental Biology, 2022
The tumor microenvironment plays an important role in cancer development and the use of 3D in vitro systems that decouple different elements of this microenvironment is critical for the study of cancer progression. In neuroblastoma (NB), vitronectin (VN),
Ezequiel Monferrer, Ezequiel Monferrer, Oana Dobre, Sara Trujillo, Mariana Azevedo González Oliva, Alexandre Trubert-Paneli, Delia Acevedo-León, Rosa Noguera, Rosa Noguera, Manuel Salmeron-Sanchez   +9 more
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