Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Silvia Passantino"'
Autor:
Silvia Passantino, Serena Chiellino, Francesca Girolami, Mattia Zampieri, Giovanni Battista Calabri, Gaia Spaziani, Elena Bennati, Giulio Porcedda, Elena Procopio, Iacopo Olivotto, Silvia Favilli
Publikováno v:
Diagnostics, Vol 13, Iss 24, p 3674 (2023)
Background: Cardiac involvement is reported in a significant proportion of patients with classical organic acidurias (OAs), contributing to disability and premature death. Different cardiac phenotypes have been described, among which dilated cardiomy
Externí odkaz:
https://doaj.org/article/fb0ac5bc409e44d3bf1ac5a64cc72c83
Autor:
Mattia Zampieri, Chiara Di Filippo, Chiara Zocchi, Vera Fico, Cristina Golinelli, Gaia Spaziani, Giovanni Calabri, Elena Bennati, Francesca Girolami, Alberto Marchi, Silvia Passantino, Giulio Porcedda, Guglielmo Capponi, Alessia Gozzini, Iacopo Olivotto, Luca Ragni, Silvia Favilli
Publikováno v:
Diagnostics, Vol 13, Iss 24, p 3666 (2023)
Restrictive cardiomyopathy (RCM) is characterized by restrictive ventricular pathophysiology determined by increased myocardial stiffness. While suspicion of RCM is initially raised by clinical evaluation and supported by electrocardiographic and ech
Externí odkaz:
https://doaj.org/article/b2e23465e3ef4ea9ad46560ae4c1eb94
Autor:
Francesca Girolami, Silvia Passantino, Adelaide Ballerini, Alessia Gozzini, Giulio Porcedda, Iacopo Olivotto, Silvia Favilli
Publikováno v:
Cardiogenetics, Vol 12, Iss 2, Pp 206-211 (2022)
Restrictive cardiomyopathy (RCM) is a rare disease of the myocardium caused by mutations in several genes including TNNT2, DES, TNNI3, MYPN and FLNC. Individuals affected by RCM often develop heart failure at a young age, requiring early heart transp
Externí odkaz:
https://doaj.org/article/3ee726417fc84954b4f6b0321f06c13b
Autor:
Gabrielle Norrish, Gali Kolt, Elena Cervi, Ella Field, Kathleen Dady, Lidia Ziółkowska, Iacopo Olivotto, Silvia Favilli, Silvia Passantino, Giuseppe Limongelli, Martina Caiazza, Marta Rubino, Anwar Baban, Fabrizio Drago, Karen Mcleod, Maria Ilina, Ruth McGowan, Graham Stuart, Vinay Bhole, Orhan Uzun, Amos Wong, Laz Lazarou, Elspeth Brown, Piers E.F. Daubeney, Amrit Lota, Grazia Delle Donne, Katie Linter, Sujeev Mathur, Tara Bharucha, Satish Adwani, Jon Searle, Anca Popoiu, Caroline B. Jones, Zdenka Reinhardt, Juan Pablo Kaski
Publikováno v:
ESC Heart Failure, Vol 8, Iss 6, Pp 5057-5067 (2021)
Abstract Aims Children presenting with hypertrophic cardiomyopathy (HCM) in infancy are reported to have a poor prognosis, but this heterogeneous group has not been systematically characterized. This study aimed to describe the aetiology, phenotype,
Externí odkaz:
https://doaj.org/article/606e02324a3e411484c1c9f074115236
Autor:
Gaia Spaziani, Francesca Bonanni, Francesca Girolami, Elena Bennati, Giovanni Battista Calabri, Chiara Di Filippo, Giulio Porcedda, Silvia Passantino, Stefano Nistri, Iacopo Olivotto, Silvia Favilli
Publikováno v:
Diagnostics, Vol 13, Iss 8, p 1490 (2023)
Background: Aortic dilation (AoD) is commonly reported in patients with bicuspid aortic valve (BAV) and has been related to flow abnormalities and genetic predisposition. AoD-related complications are reported to be extremely rare in children. Conver
Externí odkaz:
https://doaj.org/article/ea0380acb91d443c8d82fa531a8d3dcd
Autor:
Valentina Spinelli, Francesca Girolami, Chiara Marrone, Veronica Consigli, Maria Iascone, Silvia Passantino, Giulio Porcedda, Giovanni Battista Calabri, Luciano De Simone, Iacopo Olivotto, Giuseppe Santoro, Silvia Favilli
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 3368-3372 (2020)
Abstract Genetic investigation of early‐onset Dilatative cardiomyopathy phenotype, including molecular autopsy, is the key to appropriate recognition and management of rare etiologies and atypical presentations and to offer genetic counseling to th
Externí odkaz:
https://doaj.org/article/a1839f6f9f5b438fa2629f0563cfa98f
Autor:
Alice Brambilla, Iacopo Olivotto, Silvia Favilli, Gaia Spaziani, Silvia Passantino, Elena Procopio, Amelia Morrone, Maria Alice Donati
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Primary mitochondrial disorders (PMD) are rare conditions resulting in progressive multi-organ failure. Cardiovascular involvement (CVI) has been reported in paediatric patients. However, its age-related prevalence, clinical prese
Externí odkaz:
https://doaj.org/article/d56a0e27dfe544fcbedfb76da9d2d3fe
Autor:
Alessia Argirò, Mattia Zampieri, Lorenzo-Lupo Dei, Cecilia Ferrantini, Alberto Marchi, Alessia Tomberli, Katia Baldini, Francesco Cappelli, Silvia Favilli, Silvia Passantino, Chiara Zocchi, Luigi Tassetti, Martina Gabriele, Niccolò Maurizi, Niccolò Marchionni, Raffaele Coppini, Iacopo Olivotto
Publikováno v:
International Journal of Cardiology. 370:271-278
We assessed the efficacy and safety of ranolazine in real-world patients with hypertrophic cardiomyopathy (HCM).Ranolazine is an anti-anginal drug that inhibits the late phase of the inward sodium current. In a small prospective trial, ranolazine red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1fb48d655e474bfebd61fb970ddffb9
https://doi.org/10.1016/j.ijcard.2022.10.014
https://doi.org/10.1016/j.ijcard.2022.10.014
Autor:
Niccolò Maurizi, Chiara Chiriatti, Carlo Fumagalli, Mattia Targetti, Silvia Passantino, Panagiotis Antiochos, Ioannis Skalidis, Chiara Chiti, Giulia Biagioni, Alessia Tomberli, Sara Giovani, Raffaele Coppini, Franco Cecchi, Iacopo Olivotto
Publikováno v:
Journal of clinical medicine, vol. 12, no. 7, pp. 2725
Journal of Clinical Medicine; Volume 12; Issue 7; Pages: 2725
Journal of Clinical Medicine; Volume 12; Issue 7; Pages: 2725
Background: Although disopyramide has been widely used to reduce left ventricular outflow obstruction (LVOTO) and to improve symptoms in patients with obstructive hypertrophic cardiomyopathy (oHCM), its use in real world as well as patient characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeeb095e2f4199e21a537f4985f6ab63
https://serval.unil.ch/notice/serval:BIB_0F69542BC78D
https://serval.unil.ch/notice/serval:BIB_0F69542BC78D
Autor:
Martina Caiazza, Adelaide Fusco, Silvia Passantino, Francesco Di Fraia, Alfredo Mauriello, Federica Amodio, Annapaola Cirillo, Michele Lioncino, Francesco Natale, Silvia Favilli, Fabio Fimiani, Giuseppe Limongelli, Federica Verrillo, Nunzia Borrelli, Emanuele Monda, Marta Rubino, Francesca Girolami, Gioacchino Scarano
Publikováno v:
Heart Failure Clinics. 18:31-37
Friedreich ataxia (FRDA) is an autosomal recessive neurodegenerative disorder caused by a homozygous GAA triplet repeat expansion in the frataxin gene. Cardiac involvement, usually manifesting as hypertrophic cardiomyopathy, can range from asymptomat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::284661f231e0d85168000a3f532f7adc
https://doi.org/10.1016/j.hfc.2021.07.001
https://doi.org/10.1016/j.hfc.2021.07.001