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Akademický článek

Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus

Publikováno v: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)

Abstract Hereditary transthyretin amyloidosis (ATTRv, v for variant) is a late-onset, autosomal dominant disease caused by progressive extracellular deposition of transthyretin amyloid fibrils, leading to organ damage and death. For other late-onset

Externí odkaz: https://doaj.org/article/06f1cac9f11446abaa06ec95182536f4

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Akademický článek

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P278 A RARE CASE OF RECURRENT SARS–COV–2 MRNA VACCINE–INDUCED PERICARDITIS

Autor: R Mistrulli, S Orellana, E Cittadini, M Ricci, G Tini, M Musumeci, C Autore, G Tocci, E Pagannone

Publikováno v: European Heart Journal Supplements. 25:D148-D149

42–year–old man, former smoker, with allergic asthma. From February 2022, three weeks after the third dose of SARS–CoV–2 vaccine Spikevax (mRNA–1273), he experienced subcontinuous chest pain, worsened by breathing, sometimes with fever over

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3bf8ab310239377f41e19f676de182be
https://doi.org/10.1093/eurheartjsupp/suad111.352

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Incidence and risk factors for pacemaker implantation in light chain and transthyretin cardiac amyloidosis

Autor: A Porcari, M Rossi, F Cappelli, M Canepa, B Musumeci, A Cipriani, G Tini, G G Varra', A Argiro', E Sessarego, G Sinigiani, G Di Bella, C Rapezzi, G Sinagra, M Merlo

Publikováno v: European Heart Journal. 43

Background The incidence and risk factors of pacemaker (PM) implantation in patients with cardiac amyloidosis (CA) are largely unexplored. Purpose We sought to characterise the trends in the incidence of permanent PM and to identify baseline predicto

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::84029c923088cdf10f380f7daf976f7e
https://doi.org/10.1093/eurheartj/ehac544.1771

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Prognostic implications of biventricular uptake of bone tracers at planar scintigraphy in transthyretin cardiac amyloidosis

Autor: A Porcari, L Pagura, M Canepa, E Biagini, F Cappelli, G Tini, F Dore, S Longhi, R Sciagra', M Fontana, J Gillmore, C Rapezzi, M Merlo, G Sinagra

Publikováno v: European Heart Journal. 43

Background The prognostic role of bone tracer uptake in transthyretin cardiac amyloidosis (ATTR-CA) is controversial. A further characterization of cardiac retention measured by Perugini scale with differentiation between biventricular (BiV) and isol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aa3b496d7c2664b5e6e1f96eeb4bd0c0
https://doi.org/10.1093/eurheartj/ehac544.1770

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Incidence and factors associated with de novo atrial fibrillation in patients with wild-type transthyretin cardiac amyloidosis

Autor: C Fumagalli, M Zampieri, A Argiro', B Musumeci, G Tini, G Di Bella, A Cipriani, A Porcari, M Canepa, M Merlo, G Sinagra, C Rapezzi, F Perfetto, F Cappelli

Publikováno v: European Heart Journal. 43

Purpose We described the incidence and ECG factors associated with de novo atrial fibrillation (AF) in patients diagnosed with wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) to drive tailored arrhythmia screening. Background Data on the inci

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fa80e27c46fba8bbaca575725a06880d
https://doi.org/10.1093/eurheartj/ehac544.1787

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Akademický článek

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Quantifying geographical accessibility to cancer clinical trials in different income landscapes

Autor: G, Tini, D, Trapani, B A, Duso, P, Beria, G, Curigliano, P G, Pelicci, L, Mazzarella

Clinical trials are increasingly perceived as a therapeutic opportunity for cancer patients. Favoring their concentration in few high-expertise academic centers maximizes quality of data collection but poses an issue of access equality. Analytical to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f03247d1c9bffa8ba2a342aa4d071b19
http://hdl.handle.net/11311/1218632

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