| Broncho-alveolar inflammation in COVID-19 patients: a correlation with clinical outcome L Pandolfi, T Fossali, V Frangipane, S Bozzini, M Morosini, M D’Amato, ... BMC pulmonary medicine 20, 1-10, 2020 | 94 | 2020 |
| Cardiac phenotypes in hereditary muscle disorders: JACC state-of-the-art review E Arbustini, A Di Toro, L Giuliani, V Favalli, N Narula, M Grasso Journal of the American College of Cardiology 72 (20), 2485-2506, 2018 | 85 | 2018 |
| Long COVID: long-term effects? A Di Toro, A Bozzani, G Tavazzi, M Urtis, L Giuliani, R Pizzoccheri, ... European Heart Journal Supplements 23 (Supplement_E), E1-E5, 2021 | 77 | 2021 |
| Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics E Arbustini, ER Behr, L Carrier, C van Duijn, P Evans, V Favalli, ... European Heart Journal 43 (20), 1901-1916, 2022 | 44 | 2022 |
| Repression of hypoxia-inducible factor-1 contributes to increased mitochondrial reactive oxygen species production in diabetes X Zheng, S Narayanan, C Xu, SE Angelstig, J Grünler, A Zhao, A Di Toro, ... elife 11, e70714, 2022 | 37 | 2022 |
| Heart rate/blood pressure ratio as predictor of neuromediated syncope R Mereu, G De Barbieri, T Perrone, A Mugellini, A Di Toro, L Bernardi International journal of cardiology 167 (4), 1170-1175, 2013 | 30 | 2013 |
| Trained breathing-induced oxygenation acutely reverses cardiovascular autonomic dysfunction in patients with type 2 diabetes and renal disease P Esposito, R Mereu, G De Barbieri, T Rampino, A Di Toro, PH Groop, ... Acta diabetologica 53, 217-226, 2016 | 20 | 2016 |
| Genetic basis of myocarditis: myth or reality? E Arbustini, N Narula, L Giuliani, A Di Toro Myocarditis: Pathogenesis, Diagnosis and Treatment, 45-89, 2020 | 17 | 2020 |
| Diagnostic role of head-up tilt test in patients with cough syncope R Mereu, P Taraborrelli, A Sau, A Di Toro, S Halim, S Hayat, L Bernardi, ... Ep Europace 18 (8), 1273-1279, 2016 | 15 | 2016 |
| Parasympathetic stimuli on bronchial and cardiovascular systems in humans E Zannin, R Pellegrino, A Di Toro, A Antonelli, RL Dellacà, L Bernardi Plos one 10 (6), e0127697, 2015 | 15 | 2015 |
| Anderson–fabry disease A Di Toro, V Favalli, E Arbustini Journal of Cardiovascular Medicine 19, e1-e5, 2018 | 13 | 2018 |
| Myths to debunk: the non-compacted myocardium A Di Toro, L Giuliani, A Smirnova, V Favalli, A Serio, M Urtis, M Grasso, ... European Heart Journal Supplements 22 (Supplement_L), L6-L10, 2020 | 12 | 2020 |
| Arterial function can be obtained by noninvasive finger pressure waveform L Bernardi, D Gordin, M Rosengård-Bärlund, VP Mäkinen, R Mereu, ... International journal of cardiology 175 (1), 169-171, 2014 | 7 | 2014 |
| Oxalic Cardiomyopathy: Could it Influence Treatment Plans in Patients With Primary Hyperoxaluria Type 1? A Di Toro, M Urtis, L Giuliani, C Pellegrini, A Smirnova, R Galato, ... Journal of the American College of Cardiology 78 (9), 998-999, 2021 | 6 | 2021 |
| Impediments to Heart Transplantation in Adults With MELASMT-TL1:m.3243A>G Cardiomyopathy A Di Toro, M Urtis, N Narula, L Giuliani, M Grasso, M Pasotti, C Pellegrini, ... Journal of the American College of Cardiology 80 (15), 1431-1443, 2022 | 5 | 2022 |
| Common presentation of rare diseases: Aortic aneurysms & valves E Arbustini, V Favalli, A Di Toro, L Giuliani, G Limongelli International journal of cardiology 257, 358-365, 2018 | 5 | 2018 |
| Hereditary muscle diseases and the heart: the cardiologist’s perspective L Giuliani, A Di Toro, M Urtis, A Smirnova, M Concardi, V Favalli, A Serio, ... European Heart Journal Supplements 22 (Supplement_E), E13-E19, 2020 | 4 | 2020 |
| P5539 Genetic heterogeneity of spontaneous coronary artery dissection (SCAD) L Giuliani, A Di Toro, E Disabella, M Grasso, A Serio, M Urtis, A Pilotto, ... European Heart Journal 40 (Supplement_1), ehz746. 0485, 2019 | 4 | 2019 |
| Pathologic substrate of gastropathy in Anderson-Fabry disease A Di Toro, N Narula, L Giuliani, M Concardi, A Smirnova, V Favalli, M Urtis, ... Orphanet Journal of Rare Diseases 15 (1), 1-4, 2020 | 3 | 2020 |
| Renal and brain complications in GLA p. Phe113Leu Fabry disease. Comments on “Fabry disease caused by the GLA p. Phe113Leu (p. F113L) variant: Natural history in males” by … A Smirnova, A Di Toro, L Giuliani, M Tagliani, M Urtis, V Favalli, ... European Journal of Medical Genetics 63 (4), 103847, 2020 | 3 | 2020 |
