G. Buja
University of Padua
31 Papers
164 Citations
G. Buja is an academic researcher from University of Padua. The author has contributed to research in topics: Sudden death & Right ventricular cardiomyopathy. The author has an hindex of 11, co-authored 31 publications.
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Papers
The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24.
Alessandra Rampazzo,Andrea Nava,G. A. Danieli,G. Buja,Luciano Daliento,Giuseppe Fasoli,Roldano Scognamiglio,Domenico Corrado,Gaetano Thiene +8 more
TL;DR: The chromosomal localization of the disease gene is reported here for the first time and its pre-symptomatic identification by linkage analysis in the affected families strongly increases the possibility of prevention of life-threatening complications.
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Cardiac involvement in becker muscular dystrophy
Paola Melacini,Marina Fanin,Gian Antonio Danieli,Giuseppe Fasoli,Carla Villanova,Corrado Angelini,Libero Vitiello,Manuela Miorelli,G. Buja,Maria Luisa Mostacciuolo,Elena Pegoraro,Sergio Dalla Volta +11 more
TL;DR: The cardiac manifestation of Becker muscular dystrophy is characterized by early right ventricular involvement associated or not with left ventricular impairment, and exon 49 deletion is associated with cardiac disease.
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Signal-averaged electrocardiogram in patients with arrhythmogenic right ventricular cardiomyopathy and ventricular arrhythmias.
Andrea Nava,Antonio Franco Folino,Barbara Bauce,P. Turrini,G. Buja,Luciano Daliento,Gaetano Thiene +6 more
TL;DR: The signal averaged ECG is not helpful in diagnosing minor forms of the disease, but since it is a non-invasive method, it may be useful in evaluating progression of the Disease.
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Accelerated idioventricular rhythm of infundibular origin in patients with a concealed form of arrhythmogenic right ventricular dysplasia.
Bortolo Martini,Andrea Nava,G. Thiene,G. Buja,Canciani B,Miraglia G,Roldano Scognamiglio,Giovanni Boffa,Luciano Daliento +8 more
TL;DR: It is shown that some patients with accelerated idioventricular rhythm have right ventricular abnormalities that are typical of the localised and concealed forms of arrhythmogenicright ventricular dysplasia.
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•Journal Article
[The prevalence of the Wolff-Parkinson-White syndrome in a population of 116,542 young males].
TL;DR: Since 1988 to 1992, 116,452 consecutive 12-lead electrocardiograms belonging to the entire cohort of 18-year old young boys resident in Padova, Treviso, Rovigo, Venezia, Belluno area were analyzed, identifying 173 cases of overt WPW pattern.
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