Search Results - "ANASTASAKIS, ARIS"

Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria by Corrado, Domenico, Perazzolo Marra, Martina, Zorzi, Alessandro, Beffagna, Giorgia, Cipriani, Alberto, Lazzari, Manuel De, Migliore, Federico, Pilichou, Kalliopi, Rampazzo, Alessandra, Rigato, Ilaria, Rizzo, Stefania, Thiene, Gaetano, Anastasakis, Aris, Asimaki, Angeliki, Bucciarelli-Ducci, Chiara, Haugaa, Kristine H., Marchlinski, Francis E., Mazzanti, Andrea, McKenna, William J., Pantazis, Antonis, Pelliccia, Antonio, Schmied, Christian, Sharma, Sanjay, Wichter, Thomas, Bauce, Barbara, Basso, Cristina

“…The original designation of “Arrhythmogenic right ventricular (dysplasia/) cardiomyopathy”(ARVC) was used by the scientists who first discovered the disease,…”
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Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases by Pinto, Yigal M, Elliott, Perry M, Arbustini, Eloisa, Adler, Yehuda, Anastasakis, Aris, Böhm, Michael, Duboc, Denis, Gimeno, Juan, de Groote, Pascal, Imazio, Massimo, Heymans, Stephane, Klingel, Karin, Komajda, Michel, Limongelli, Giuseppe, Linhart, Ales, Mogensen, Jens, Moon, James, Pieper, Petronella G, Seferovic, Petar M, Schueler, Stephan, Zamorano, Jose L, Caforio, Alida L P, Charron, Philippe

“…In this paper the Working Group on Myocardial and Pericardial Disease proposes a revised definition of dilated cardiomyopathy (DCM) in an attempt to bridge the…”
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Diagnosis and management of myocardial involvement in systemic immune-mediated diseases: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Disease by Caforio, Alida L P, Adler, Yehuda, Agostini, Carlo, Allanore, Yannick, Anastasakis, Aris, Arad, Michael, Böhm, Michael, Charron, Philippe, Elliott, Perry M, Eriksson, Urs, Felix, Stephan B, Garcia-Pavia, Pablo, Hachulla, Eric, Heymans, Stephane, Imazio, Massimo, Klingel, Karin, Marcolongo, Renzo, Matucci Cerinic, Marco, Pantazis, Antonis, Plein, Sven, Poli, Valeria, Rigopoulos, Angelos, Seferovic, Petar, Shoenfeld, Yehuda, Zamorano, Josè L, Linhart, Ales

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Practical recommendations for the diagnosis and management of transthyretin cardiac amyloidosis by Bistola, Vasiliki, Parissis, John, Foukarakis, Emmanouil, Valsamaki, Pipitsa N., Anastasakis, Aris, Koutsis, Georgios, Efthimiadis, Georgios, Kastritis, Efstathios

“…Cardiac amyloidosis (CA) is an infiltrative restrictive cardiomyopathy caused by accumulation in the heart interstitium of amyloid fibrils formed by misfolded…”
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A truncating variant altering the extreme C-terminal region of desmoplakin (DSP) suggests the crucial functional role of the region: a case report study by Pantou, Malena P, Gourzi, Polyxeni, Vlagkouli, Vasiliki, Papatheodorou, Efstathios, Tsoutsinos, Alexandros, Nyktari, Eva, Degiannis, Dimitrios, Anastasakis, Aris

“…Homozygous truncating mutations located in the C-terminal region of the desmoplakin gene (DSP) are known to mainly cause Carvajal syndrome, an autosomal…”
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Genetics of Heritable Thoracic Aortic Disease by Papatheodorou, Efstathios, Degiannis, Dimitrios, Anastasakis, Aris

“…Genetic testing plays an increasing diagnostic and prognostic role in the management of patients with heritable thoracic aortic disease (HTAD). The…”
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Current perspectives on the diagnosis and management of dilated cardiomyopathy Beyond heart failure: a Cardiomyopathy Clinic Doctor's point of view by Bakalakos, Athanasios, Ritsatos, Konstantinos, Anastasakis, Aris

“…Left ventricular enlargement and dysfunction are fundamental components of dilated cardiomyopathy (DCM). DCM is a major cause of heart failure and cardiac…”
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Current and emerging perspectives on pathophysiology, diagnosis, and management of hypertrophic cardiomyopathy by Gartzonikas, Ilias K., Naka, Katerina K., Anastasakis, Aris

“…Hypertrophic cardiomyopathy (HCM) is the most common genetically inherited cardiomyopathy with an autosomal dominant inheritance pattern. A disease-causing…”
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Epidemiology of Pediatric Cardiomyopathy in a Mediterranean Population by Bagkaki, Alena, Parthenakis, Fragiskos, Chlouverakis, Gregory, Anastasakis, Aris, Papagiannis, Ioannis, Galanakis, Emmanouil, Germanakis, Ioannis

“…Our knowledge regarding the epidemiology of pediatric cardiomyopathy is based on large national population studies reporting an annual incidence of 1 case per…”
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Fabry disease and cardiovascular involvement by Anastasakis, Aris, Papatheodorou, Efstathios, Steriotis, Alexandros Klavdios

“…Fabry disease (FD, OMIM 301500) is a rare X-linked lysosomal storage disorder of the glycosphigolipid metabolism caused by total or partial deficiency of the…”
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Clinical Significance of Epsilon Waves in Arrhythmogenic Cardiomyopathy by PROTONOTARIOS, ALEXANDROS, ANASTASAKIS, ARIS, TSATSOPOULOU, ADALENA, ANTONIADES, LOIZOS, PRAPPA, EFSTATHIA, SYRRIS, PETROS, TOUSOULIS, DIMITRIOS, McKENNA, WILLIAM J., PROTONOTARIOS, NIKOS

“…Epsilon Waves in ACM Introduction Epsilon waves are hallmark features of arrhythmogenic cardiomyopathy (ACM) but information about their clinical significance…”
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Cardiomyopathies in children: An overview by Tsatsopoulou, Adalena, Protonotarios, Ioannis, Xylouri, Zafeirenia, Papagiannis, Ioannis, Anastasakis, Aris, Germanakis, Ioannis, Patrianakos, Alexandros, Nyktari, Evangelia, Gavras, Christoforos, Papadopoulos, Georgios, Meditskou, Soultana, Lazarou, Emilia, Miliou, Antigoni, Lazaros, George

“…Paediatric cardiomyopathies form a heterogeneous group of disorders characterized by structural and electrical abnormalities of the heart muscle, commonly due…”
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Mitral valve in hypertrophic cardiomyopathy: a three-dimensional transesophageal study by Venieri, Erifili, Aggeli, Constantina, Anastasakis, Aris, Sambatakou, Helen, Stefanadis, Christodoulos, Tousoulis, Dimitrios

“…It is reported that the mitral valve (MV) in hypertrophic cardiomyopathy (HCM) has structural abnormalities. To assess the MV in HCM patients using…”
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Atrial fibrillation in hypertrophic cardiomyopathy – A contemporary mini-review by Dragasis, Stylianos, Vlachos, Konstantinos, Kariki, Ourania, Koskina, Stavroula, Zygouri, Andromahi, Patsiotis, Ilias G., Anastasakis, Aris, Athanasopoulos, George, Ritsatos, Konstantinos, Letsas, Konstantinos, Efremidis, Michael

“…Hypertrophic cardiomyopathy (HCM) represents the most common genetically inherited cardiovascular disorder and a leading cause of heart failure and sudden…”
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Remodeling of myocyte gap junctions in arrhythmogenic right ventricular cardiomyopathy due to a deletion in plakoglobin (Naxos disease) by Kaplan, Starr R, Gard, Joseph J, Protonotarios, Nikos, Tsatsopoulou, Adalena, Spiliopoulou, Chara, Anastasakis, Aris, Squarcioni, Catherine Prost, McKenna, William J, Thiene, Gaetano, Basso, Cristina, Brousse, Nicole, Fontaine, Guy, Saffitz, Jeffrey E

“…We tested the hypothesis that defective interactions between adhesion junctions and the cytoskeleton caused by the plakoglobin mutation in Naxos disease lead…”
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Risk and Protective Factors for Sudden Cardiac Death: An Umbrella Review of Meta-Analyses by Tsartsalis, Dimitrios, Korela, Dafni, Karlsson, Lars O., Foukarakis, Emmanouil, Svensson, Anneli, Anastasakis, Aris, Venetsanos, Dimitrios, Aggeli, Constantina, Tsioufis, Costas, Braunschweig, Frieder, Dragioti, Elena, Charitakis, Emmanouil

“…Background Sudden cardiac death (SCD) is a global public health issue, accounting for 10–20% of deaths in industrialized countries. Identification of…”
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Proposed algorithm for return to sports in competitive athletes who have suffered COVID-19 by Oikonomou, Evangelos, Papanikolaou, Angelos, Anastasakis, Aris, Bournousouzis, Elefterios, Georgakopoulos, Christos, Goudevenos, John, Ioakeimidis, Nikolaos, Kanakakis, John, Lazaros, George, Papatheodorou, Stathis, Tsatsopoulou, Adalena, Tsonou, Paraskevi, Vogiatzi, Georgia, Panagiotakopoulos, George, Tousoulis, Dimitris, Vlachopoulos, Charalambos

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Mutations in the Gene for Cardiac Myosin-Binding Protein C and Late-Onset Familial Hypertrophic Cardiomyopathy by Niimura, Hideshi, Bachinski, Linda L, Sangwatanaroj, Somkiat, Watkins, Hugh, Chudley, Albert E, McKenna, William, Kristinsson, Arni, Roberts, Robert, Sole, Michael, Maron, Barry J, Seidman, Christine E, Seidman, J.G, Thierfelder, Ludwig, Jarcho, John A, Anastasakis, Aris, Toutouzas, Pavlos, Elstein, Eleanor, Liew, Choong-Chin, Liew, Jack, Mably, John, Rakowski, Harry, Wigle, E. Douglas, Zhao, Minshun, Salerni, Rosemarie, Bjornsdottir, Halldora

“…Hypertrophic cardiomyopathy, a disorder occurring in approximately 1 of every 500 people, causes a broad spectrum of pathological findings and clinical…”
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Arrhythmic Mitral Valve Prolapse: Implications for Family Screening and Sports Participation Eligibility by Papatheodorou, Efstathios, Anastasakis, Aris

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Dilated cardiomyopathy in the era of precision medicine: latest concepts and developments by Orphanou, Nicoletta, Papatheodorou, Efstathios, Anastasakis, Aris

“…Dilated cardiomyopathy (DCM) is an umbrella term entailing a wide variety of genetic and non-genetic etiologies, leading to left ventricular systolic…”
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