Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Fabiana Romeo"'
Autor:
Elisa Silvetti, Oreste Lanza, Fabiana Romeo, Annamaria Martino, Elisa Fedele, Chiara Lanzillo, Cinzia Crescenzi, Francesca Fanisio, Leonardo Calò
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
Cardiomyopathies are a heterogeneous group of pathologies characterized by structural and functional alterations of the heart. Recent technological advances in cardiovascular imaging offer an opportunity for deep phenotypic and etiological definition
Externí odkaz:
https://doaj.org/article/387f188afaff4109a721630c7f4c9f1b
Autor:
Francesca Di Lorenzo, Enrica Marchionni, Valentina Ferradini, Andrea Latini, Laura Pezzoli, Annamaria Martino, Fabiana Romeo, Annamaria Iorio, Stefano Bianchi, Maria Iascone, Leonardo Calò, Giuseppe Novelli, Ruggiero Mango, Federica Sangiuolo
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 2490 (2023)
Variants in desmoplakin gene (DSP MIM *125647) have been usually associated with Arrhythmogenic Cardiomyopathy (ACM), or Dilated Cardiomyopathy (DCM) inherited in an autosomal dominant manner. A cohort of 18 probands, characterized as heterozygotes f
Externí odkaz:
https://doaj.org/article/b8e1fd48173e4a15861d5b08b86b0ff4
Autor:
Ibrahim El‐Battrawy, Francesco Santoro, Thomas Stiermaier, Christian Möller, Francesca Guastafierro, Giuseppina Novo, Salvatore Novo, Enrica Mariano, Francesco Romeo, Fabiana Romeo, Holger Thiele, Federico Guerra, Alessandro Capucci, Irene Giannini, Natale Daniele Brunetti, Ingo Eitel, Ibrahim Akin
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 8, Iss 9 (2019)
Background Current literature only reports variable information from single‐center studies on the recurrence rate, the complications, and the outcome of patients with Takotsubo syndrome (TTS) experiencing recurrent TTS. Therefore, a detailed descri
Externí odkaz:
https://doaj.org/article/1772c02aa8b04ced97958b00ae84dc42
Autor:
Cinzia Crescenzi, Elisa Silvetti, Fabiana Romeo, Annamaria Martino, Edoardo Bressi, Germana Panattoni, Matteo Stefanini, Alessandra Stazi, Maria Ludovica Danza, Marco Rebecchi, Stefano Canestrelli, Elisa Fedele, Oreste Lanza, Chiara Lanzillo, Armando Fusco, Paolo Golia, Ermenegildo De Ruvo, Leonardo Calò
Publikováno v:
European Heart Journal Supplements. 25:C179-C184
This article summarizes the main electrocardiogram (ECG) findings in dilated cardiomyopathy (DCM) patients. Recent reports are described in the great ‘pot’ of DCM peculiar ECG patterns that are typical of specific forms of DCM. Patients with late
Autor:
Chiara Lanzillo, Elisa Fedele, Annamaria Martino, Alessandro Ferrazza, Armando Fusco, Elisa Silvetti, Stefano Canestrelli, Fabiana Romeo, Emanuele Canali, Lucia De Luca, Paolo Golia, Cinzia Crescenzi, Matteo Stefanini, Leonardo Calò
Publikováno v:
European Heart Journal Supplements. 25:C200-C204
Fabry disease (FD) is a rare X-linked inherited lysosomal storage disorder caused by deficient a-galactosidase A activity that leads to an accumulation of glycolipids, mainly globotriaosylceramide (Gb3) and globotriaosylsphingosine, in affected tissu
Autor:
Leonardo Calò, Giada Oliviero, Cinzia Crescenzi, Fabiana Romeo, Annamaria Martino, Edoardo Bressi, Matteo Stefanini, Elisa Silvetti, Ludovica Danza, Marco Rebecchi, Stefano Canestrelli, Elisa Fedele, Chiara Lanzillo, Armando Fusco, Ermenegildo De Ruvo
Publikováno v:
European Heart Journal Supplements. 25:C169-C172
Criteria for diagnosis of arrhythmogenic cardiomyopathy (ACM) were first proposed in 1994 and subsequently revised in 2010 and in 2020 by an international task force. According to the last consensus of 2020, ACM is defined as a heart muscle disease a
Autor:
Leonardo Calò, Oreste Lanza, Cinzia Crescenzi, Cristian Parisi, Germana Panattoni, Annamaria Martino, Marco Rebecchi, Pierpaolo Tarzia, Pellegrino Ciampi, Fabiana Romeo, Stefano Canestrelli, Elisa Silvetti, Ermenegildo De Ruvo
Publikováno v:
European Heart Journal Supplements. 25:C218-C226
Sudden cardiac death (SCD) can be caused by several clinical conditions, overt or misconceived, which recognize different pathophysiologies determining the development of fatal arrhythmic events. In the various forms of structural heart disease such
Autor:
Francesco Romeo, Irene Giannini, Federico Guerra, Ibrahim Akin, Thomas Stiermaier, Giuseppina Novo, Enrica Mariano, Natale Daniele Brunetti, Ingo Eitel, Ibrahim El-Battrawy, Fabiana Romeo, Francesca Guastafierro, Salvatore Novo, Holger Thiele, Christian Möller, Francesco Santoro, Alessandro Capucci
Publikováno v:
Chest. 160:1433-1441
Background The short- and long-term prognosis of Takotsubo syndrome (TTS) presenting with right ventricular (RV) involvement remains poorly understood. Research Question What is the incidence and clinical outcome of RV involvement in TTS? Study Desig
Autor:
Ruggiero Mango, Claudia De Masi, Giovanni Parlapiano, Leonardo Calò, Valentina Ferradini, Francesco Fedele, Federica Sangiuolo, Giuseppe Novelli, Paola Spitalieri, Sara Mannucci, Annamaria Martino, Fabiana Romeo, Francesca Di Lorenzo, Michela Murdocca, Joseph Cosma
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 21
Journal of Clinical Medicine, Vol 10, Iss 5075, p 5075 (2021)
Volume 10
Issue 21
Journal of Clinical Medicine, Vol 10, Iss 5075, p 5075 (2021)
Dilated cardiomyopathy (DCM) refers to a spectrum of heterogeneous myocardial disorders characterized by ventricular dilation and depressed myocardial performance in the absence of hypertension, valvular, congenital, or ischemic heart disease. Mutati
Autor:
Pasquale Caldarola, Christian Möller, Salvatore Novo, Irene Giannini, Holger Thiele, Natale Daniele Brunetti, Francesco Santoro, Giuseppina Novo, Ibrahim Akin, Francesco Romeo, Thomas Stiermaier, Andrea Santangelo, Ingo Eitel, Federico Guerra, Francesca Guastafierro, Enrica Mariano, Fabiana Romeo, Alessandro Capucci, Ibrahim El-Battrawy
Publikováno v:
Heart Failure Reviews. 25:505-511
One important complication related to takotsubo syndrome (TTS) is adverse rhythm disorders. Our study was conducted to determine the incidence and management of adverse rhythm disorders in TTS and its long-term prognostic impact. We analyzed 906 TTS