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Journal of Hypertension|February 11, 2014
Prognostic value of depressed midwall systolic function in cardiac light-chain amyloidosisStefano Perlini, Francesco Salinaro, Francesco Musca, et al.
European Journal of Human Genetics : EJHG|November 15, 2022
Investigation on the high recurrence of the ATTRv-causing transthyretin variant Val142Ile in central ItalyFrancesco Mazzarotto, Alessia Argirò, Mattia Zampieri, et al.
Clinical Epigenetics|November 18, 2020
Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosisAntonella De Lillo, Gita A Pathak, Flavio De Angelis, et al.
International Journal of Cardiology|January 6, 2022
Sex-related differences in clinical presentation and all-cause mortality in patients with cardiac transthyretin amyloidosis and light chain amyloidosisMattia Zampieri, Alessia Argirò, Marco Allinovi, et al.
Aging Clinical and Experimental Research|May 2, 2023
Frailty and caregiver relationship quality in older patients diagnosed with transthyretin cardiac amyloidosisCarlo Fumagalli, Martina Smorti, Lucia Ponti, et al.
International Journal of Cardiology|February 7, 2018
Lung uptake during 99mTc-hydroxymethylene diphosphonate scintigraphy in patient with TTR cardiac amyloidosis: An underestimated phenomenonFrancesco Cappelli, Chiara Gallini, Egidio Natalino Costanzo, et al.
Giornale Italiano Di Cardiologia (2006)|July 26, 2021
[Approach to the diagnosis and management of patients with cardiac amyloidosis. A consensus document by the Tuscan section of the Italian Association of Hospital Cardiologists (ANMCO) and the Tusco-Umbrian section of the Italian Society of Cardiology (SIC)]Michele Emdin, Federico Perfetto, Alberto Aimo, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 13, 2014
Biohumoral markers as predictor of right ventricular dysfunction in AL AmyloidosisFrancesco Cappelli, Samuele Baldasseroni, Franco Bergesio, et al.
Internal and Emergency Medicine|September 12, 2020
Poor right ventricular function is associated with impaired exercise capacity and ventilatory efficiency in transthyretin cardiac amyloid patientsSimone Bartolini, Samuele Baldasseroni, Francesco Fattirolli, et al.
Pharmacogenomics and Personalized Medicine|May 20, 2022
Italian Real-Life Experience of Patients with Hereditary Transthyretin Amyloidosis Treated with PatisiranVincenzo Di Stefano, Antonella Fava, Luca Gentile, et al.
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