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La Radiologia Medica|February 11, 2024
Body CT examinations in oncologic patients: the impact of subspecialty radiology on radiation exposure in the clinical practice. A quality care studyStefania Rizzo, Luca Bellesi, Andrea D'Ermo, et al.
Congenital Heart Disease|September 8, 2016
Aortic stenting in the growing sheep causes aortic endothelial dysfunction but not hypertension: Clinical implications for coarctation repairNicola Maschietto, Luca Semplicini, Giulio Ceolotto, et al.
International Journal of Cardiology|December 8, 2018
Impact of systemic immune-mediated diseases on clinical features and prognosis of patients with biopsy-proved myocarditisGiovanni Peretto, Simone Sala, Giacomo De Luca, et al.
Communications Medicine|February 6, 2026
Integrative genomic and literature assessment of desmoglein 2-related arrhythmogenic cardiomyopathy with Italian cohort validationSerena Pinci, Rudy Celeghin, Marika Martini, et al.
Pathologica|May 20, 2024
Cardiovascular pathology in vasculitisMonica De Gaspari, Andrea Ascione, Chiara Baldovini, et al.
Cardiovascular Research|March 10, 2018
Loss of cardiac Wnt/β-catenin signalling in desmoplakin-deficient AC8 zebrafish models is rescuable by genetic and pharmacological interventionAlice Giuliodori, Giorgia Beffagna, Giulia Marchetto, et al.
Current Oncology (Toronto, Ont.)|November 10, 2022
Everything You Always Wanted to Know about Sarcopenia but Were Afraid to Ask: A Quick Guide for Radiation Oncologists (Impact of Sarcopenia in Radiotherapy: The AFRAID Project)Federica Medici, Stefania Rizzo, Milly Buwenge, et al.
Journal of Personalized Medicine|November 27, 2021
Radiomics and Artificial Intelligence in Uterine Sarcomas: A Systematic ReviewGloria Ravegnini, Martina Ferioli, Alessio Giuseppe Morganti, et al.
American Journal of Medical Genetics. Part A|July 14, 2019
GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrumDoris Škorić-Milosavljević, Fleur V Y Tjong, Julien Barc, et al.
Heart Rhythm|July 17, 2018
Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)Svitlana Podliesna, Julian Delanne, Lindsey Miller, et al.
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