A. Anastasakis

发表

D. Panagiotakos, C. Stefanadis, A. Rigopoulos, 2005, Heart.

The Human Genome: Implications for Medicine and Society

P. Toutouzas, A. Anastasakis, 2002 .

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)

A. Crosby, W. McKenna, A. Coonar, 2000, The Lancet.

Effects of mutations and genetic overlap in inherited long-QT and Brugada arrhythmia syndromes.

C. Stefanadis, A. Anastasakis, C. Kotta, 2012, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

Genotype-phenotype assessment in autosomal recessive arrhythmogenic right ventricular cardiomyopathy (Naxos disease) caused by a deletion in plakoglobin.

W. Mckenna, D. Panagiotakos, P. Toutouzas, 2001, Journal of the American College of Cardiology.

Definition and treatment of arrhythmogenic cardiomyopathy: an updated expert panel report

P. Lambiase, H. Calkins, D. Corrado, 2019, European journal of heart failure.

Dilated cardiomyopathy in the era of precision medicine: latest concepts and developments

A. Anastasakis, N. Orphanou, E. Papatheodorou, 2021, Heart Failure Reviews.

Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells

H. Calkins, A. Kleber, D. Judge, 2016, Circulation. Arrhythmia and electrophysiology.

Sudden Arrhythmic Death: Family Evaluation Identifies the Cause

C. Stefanadis, A. Anastasakis, A. Vouliotis, 2015 .

Remodeling of myocyte gap junctions in arrhythmogenic right ventricular cardiomyopathy due to a deletion in plakoglobin (Naxos disease).

G. Thiene, C. Basso, J. Saffitz, 2004, Heart rhythm.

Electromyographic evidence of subclinical myopathy in hypertrophic cardiomyopathy

P. Toutouzas, C. Stefanadis, N. Karandreas, 2000, Muscle & nerve.

Arrhythmogenic right ventricular cardiomyopathy/dysplasia on the basis of the revised diagnostic criteria in affected families with desmosomal mutations

G. Thiene, C. Basso, C. Stefanadis, 2011, European heart journal.

A patient with ventricular tachycardia due to a novel mutation of the lamin A/C gene: case presentation and mini review.

A. Anastasakis, K. Lampropoulos, Themistoklis A Iliopoulos, 2013, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

Pathological electrocardiogram in a young sports champion: sign of athlete's heart or sub-clinical heart disease?

C. Stefanadis, S. Kounas, A. Anastasakis, 2009, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

Ventricular tachycardia in patients with family history of sudden cardiac death, normal coronaries and normal ventricular function. Can cardiac magnetic resonance add to diagnosis?

C. Stefanadis, G. Kolovou, S. Mavrogeni, 2013, International journal of cardiology.

Dilated cardiomyopathy in the era of precision medicine: latest concepts and developments

A. Anastasakis, N. Orphanou, E. Papatheodorou, 2021, Heart Failure Reviews.

Usefulness of noninvasive detection of left ventricular diastolic abnormalities during isometric stress in hypertrophic cardiomyopathy and in athletes.

P. Toutouzas, M. Kyriakidis, A. Rigopoulos, 1998, The American journal of cardiology.

"Primary" dilated hearts.

C. Basso, A. Anastasakis, 2018, International journal of cardiology.

Paradoxical low-flow low-gradient severe aortic stenosis in a woman with apical hypertrophy.

D. Tousoulis, C. Aggeli, A. Anastasakis, 2017, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement

M. Link, R. Hauer, H. Calkins, 2015, European heart journal.

Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

M. Link, R. Hauer, H. Calkins, 2015, Circulation.

Arrhythmogenic Right Ventricular Cardiomyopathy: The Challenge of Genetic Interpretation in Clinically Suspected Cases

C. Stefanadis, A. Anastasakis, N. Protonotarios, 2012, Cardiology.

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.

D. Panagiotakos, C. Stefanadis, P. Syrris, 2006, European heart journal.

Prevention of sudden cardiac death in the young: targeted evaluation of those at risk.

C. Stefanadis, W. McKenna, A. Anastasakis, 2006, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

"Petrified" right ventricle in long-standing naxos arrhythmogenic right ventricular cardiomyopathy.

G. Thiene, C. Basso, A. Anastasakis, 2001, Circulation.

Myelodysplasia and Naxos disease: a novel pathogenetic association?

D. Anagnostou, A. Anastasakis, N. Protonotarios, 2002, Leukemia.

Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria ScienceDirect Journal of

A. Mazzanti, D. Corrado, F. Marchlinski, 2020 .

Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria.

A. Mazzanti, D. Corrado, F. Marchlinski, 2020, International journal of cardiology.

Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.

D. Panagiotakos, C. Stefanadis, P. Syrris, 2016, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Anderson-Fabry disease: a cardiomyopathy that can be cured.

C. Stefanadis, A. Anastasakis, E. Sevdalis, 2011 .

Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator

C. Basso, J. Mogensen, M. Pavlou, 2022, European heart journal.

Response to Letter Regarding Article, "Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus Statement".

M. Link, R. Hauer, H. Calkins, 2016, Circulation.

Clinical features of hypertrophic cardiomyopathy caused by an Arg278Cys missense mutation in the cardiac troponin T gene.

P. Toutouzas, A. Miliou, C. Stefanadis, 2004, The American journal of cardiology.

Phenotype reveals genotype in a Greek long QT syndrome family.

C. Stefanadis, B. Wollnik, A. Anastasakis, 2006, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Implantable Defibrillator Therapy in Naxos Disease

P. Toutouzas, P. Toutouzas, K. Gatzoulis, 2000, Pacing and clinical electrophysiology : PACE.

Syncope in hypertrophic cardiomyopathy (part II): An expert consensus statement on the diagnosis and management.

G. Parati, A. Wilde, S. Ommen, 2022, International journal of cardiology.

D313Y Variant in Fabry Disease

Maria Papadopoulou, C. Vlachopoulos, M. Stefanou, 2022, Neurology.

Sudden unexplained death in the young: epidemiology, aetiology and value of the clinically guided genetic screening

D. Tousoulis, E. Agapitos, C. Spiliopoulou, 2018, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Genetics of Heritable Thoracic Aortic Disease

A. Anastasakis, D. Degiannis, E. Papatheodorou, 2022, Cardiogenetics.

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

J. Saffitz, C. Stefanadis, E. Ehler, 2010, Cardiovascular research.

Recommendations for interpretation of 12-lead electrocardiogram in the athlete.

Barry J Maron, Hein Heidbuchel, Pietro Delise, 2009, European heart journal.

Atrial substrate characterization in patients with atrial fibrillation and hypertrophic cardiomyopathy: Evidence for an extensive fibrotic disease.

G. Bazoukis, K. Letsas, K. Vlachos, 2021, Journal of electrocardiology.

Depression in patients with hypertrophic cardiomyopathy: is there any relation with the risk factors for sudden death?

P. Toutouzas, C. Stefanadis, A. Igoumenou, 2012, Heart Asia.

Sudden cardiac death: investigation of the classical risk factors in a community-based hypertrophic cardiomyopathy cohort.

C. Stefanadis, A. Rigopoulos, A. Anastasakis, 2013, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

Prevention of sudden cardiac death with implantable cardioverter-defibrillators in children and adolescents with hypertrophic cardiomyopathy.

M. Link, E. Ashley, G. Boriani, 2013, Journal of the American College of Cardiology.

Subclinical skeletal muscle abnormalities in patients with hypertrophic cardiomyopathy and their relation to clinical characteristics.

D. Panagiotakos, P. Toutouzas, P. Elliott, 2003, International journal of cardiology.

Optimal branch selection in alcohol septal ablation.

C. Stefanadis, K. Toutouzas, M. Vavuranakis, 2011, International journal of cardiology.

Cardiomyopathies in Children: An overview.

A. Miliou, Alexandros Patrianakos, E. Nyktari, 2023, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

Clinical Significance of Epsilon Waves in Arrhythmogenic Cardiomyopathy

P. Syrris, D. Tousoulis, W. McKenna, 2015, Cardiovascular Electrophysiology.

Myocardial Injury Induced by Radiofrequency and Low Energy Ablation: A Quantitative Study of CK Isoforms, CK‐MB, and Troponin‐T Concentrations

A. Camm, A. Camm, J. Poloniecki, 1998, Pacing and clinical electrophysiology : PACE.

Low prevalence of cardiac troponin T mutations in a Greek hypertrophic cardiomyopathy cohort

P. Toutouzas, A. Miliou, C. Stefanadis, 2005, Heart.

Mitral valve in hypertrophic cardiomyopathy: a three-dimensional transesophageal study.

C. Stefanadis, D. Tousoulis, C. Aggeli, 2019, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

A De Novo Novel Cardiac Ryanodine Mutation (Ser4155Tyr) Associated with Catecholaminergic Polymorphic Ventricular Tachycardia

V. Vassilikos, S. Paraskevaidis, I. Styliadis, 2013, Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc.

A Case of Asymptomatic Brugada Electrocardiographic Pattern Incidentally Unmasked During the Recovery Phase of an Exercise Stress Test

C. Stefanadis, S. Archontakis, A. Anastasakis, 2011 .

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.

H Niimura, A E Chudley, J. Seidman, 1998, The New England journal of medicine.

Remodeling of gap junctions in Naxos disease: a potential mechanism of lethal arrhythmias in arrhythmogenic right ventricular cardiomyopathy

C. Basso, J. Saffitz, W. McKenna, 2004 .

Hypertrophic cardiomyopathy in Greece: clinical course and outcome.

F. Triposkiadis, J. Gialafos, A. Anastasakis, 1998, Chest.

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

J. Saffitz, C. Stefanadis, E. Ehler, 2010, Cardiovascular research.

Cardiovascular pre-participation screening of young competitive athletes for prevention of sudden death: proposal for a common European protocol Consensus Statement of the Study Group of Sport Cardiology of the Working Group of Cardiac Rehabilitation and

It Istituto Superiore di Sanit, H. Heidbuchel, S. Priori, 2005 .

P. Nihoyannopoulos, C. Rapezzi, J. Mogensen, 2015 .

Recommendations for the cardiovascular screening of athletes.

P. Vardas, J. Lekakis, C. Stefanadis, 2010, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

Clinical Significance of Epsilon Waves in Arrhythmogenic Cardiomyopathy

P. Syrris, D. Tousoulis, W. McKenna, 2015, Journal of cardiovascular electrophysiology.

Corrigendum to: ‘Recommendations for interpretation of 12-lead electrocardiogram in the athlete’ [Eur Heart J 2010;31:243–259]

M. Link, H. Heidbuchel, P. Schwartz, 2010 .

Clinical Investigations: CardiologyHypertrophic Cardiomyopathy in Greece: Clinical Course and Outcome

F. Triposkiadis, J. Gialafos, M. Kyriakidis, 1998 .

Clinical significance of small nerve fiber involvement in the early diagnosis and treatment of patients with Fabry disease

G. Tsivgoulis, A. Anastasakis, C. Zompola, 2023, Journal of the Neurological Sciences.

P. Nihoyannopoulos, C. Rapezzi, J. Mogensen, 2015 .

Anderson-Fabry disease: a cardiomyopathy that can be cured.

C. Stefanadis, A. Anastasakis, E. Sevdalis, 2011, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.