Gimeno, Juan R., Tomé-Esteban, Maite, Lofiego, Carla, Hurtado, José, Pantazis, Antonios, Mist, Bryan, ...
Background Non-sustained ventricular tachycardia (NSVT) during ambulatory electrocardiographic monitoring (typically occurring at rest or during sleep) is associated with an increased risk of sudden...
Part III: Molecular Basis of Cardiac (2008)
Silvia G. Priori, Jacques Barhanin, Wilhelm Haverkamp, J. Jongsma, André G. Kleber, ...
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EROC: A Toolkit for Building NEAT0 Query Optimizers (2008)
William J. Mckenna, Louis Burger, Chi Hoang, Melissa Truong
EROC (Extensible, Reusable Optimization Components) is a toolkit for building query optimizers. EROC’s components are C++ classes based on abstractions we have iden-tified as central to query...
Behr, Elijah R., Dalageorgou, Chrysoula, Christiansen, Michael, Syrris, Petros, Hughes, Sian, Tome Esteban, Maria T., ...
Aims At least 4% of sudden deaths are unexplained at autopsy [sudden arrhythmic death syndrome (SADS)] and a quarter may be due to inherited cardiac disease. We hypothesized that comprehensive...
Jacques, Adam M., Briceno, Natalia, Messer, Andrew E., Gallon, Clare E., Jalilzadeh, Shapour, Garcia, Edwin, ...
Aim The aim of the study was to compare the functional and structural properties of the motor protein, myosin, and isolated myocyte contractility in heart muscle excised from hypertrophic...
The new European definition of cardiomyopathies: which space for muscle dystrophies?: reply (2008)
Elliott, Perry, Andersson, Bert, Arbustini, Eloisa, Bilinska, Zofia, Cecchi, Franco, Charron, Philippe, ...
Elliott, Perry, Andersson, Bert, Arbustini, Eloisa, Bilinska, Zofia, Cecchi, Franco, Charron, Philippe, ...
In biology, classification systems are used to promote understanding and systematic discussion through the use of logical groups and hierarchies. In clinical medicine, similar principles are used to...
What do tachycardiomyopathy belong to?: reply (2008)
Elliott, Perry, Andersson, Bert, Arbustini, Eloisa, Bilinska, Zofia, Cecchi, Franco, Charron, Philippe, ...
Variable interatrial conduction illustrated in a hypertrophic cardiomyopathy population. (2007)
Holmqvist, Fredrik, Platonov, Pyotr G, Carlson, Jonas, Havmoller, Rasmus, Waktare, Johan E P, McKenna, William J, ...
Abstract is not available
Syrris, Petros, Ward, Deirdre, Asimaki, Angeliki, Evans, Alison, Sen-Chowdhry, Srijita, Hughes, Sian E., ...
Aims Mutations in the desmoglein-2 (DSG2) gene have been reported in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) but clinical information regarding the associated phenotype...
Antoniades, Loizos, Tsatsopoulou, Adalena, Anastasakis, Aris, Syrris, Petros, Asimaki, Angeliki, Panagiotakos, Demosthenes, ...
Aims To evaluate clinical disease expression, non-invasive diagnosis, and prognosis in families with dominant vs. recessive arrhythmogenic right ventricular cardiomyopathy (ARVC) due to mutations in...
Elliott, Perry M., Gimeno, Juan R., Tomé, María T., Shah, Jaymin, Ward, Deirdre, Thaman, Rajesh, ...
Aims Left ventricular outflow tract obstruction (LVOTO) is associated with reduced survival in patients with hypertrophic cardiomyopathy (HCM). The influence of LVOTO on survival from SD in relation...
Antoniades, Loizos, Tsatsopoulou, Adalena, Anastasakis, Aris, Syrris, Petros, Asimaki, Angeliki, Panagiotakos, Demosthenes, ...
Aims To evaluate clinical disease expression, non-invasive diagnosis, and prognosis in families with dominant vs. recessive arrhythmogenic right ventricular cardiomyopathy (ARVC) due to mutations in...
Elliott, Perry M., Gimeno, Juan R., Tomé, María T., Shah, Jaymin, Ward, Deirdre, Thaman, Rajesh, ...
Aims Left ventricular outflow tract obstruction (LVOTO) is associated with reduced survival in patients with hypertrophic cardiomyopathy (HCM). The influence of LVOTO on survival from SD in relation...
Anastassakis, Aris, Bjørnstad, Hans Halvor, ...
Afd. Hypertensie/cardiovasc. revalidatie.
Pelliccia, Antonio, Bjørnstad, Hans Halvor, Biffi, Alessandro, Borjesson, Mats, ...
The 1996 American Heart Association consensus panel recommendations stated that pre-participation cardiovascular screening for young competitive athletes is justifiable and compelling on ethical,...
Natural history and familial characteristics of isolated left ventricular non-compaction (2005)
Murphy, Ross T., Thaman, Rajesh, Blanes, Juan Gimeno, Ward, Deirdre, Sevdalis, Elias, Papra, Efi, ...
Aims Non-compaction of the left ventricle (LVNC) is a disorder of endomyocardial morphogenesis that results in multiple trabeculations in the left ventricular myocardium. The current literature...
Pelliccia, Antonio, Fagard, Robert, Bjørnstad, Hans Halvor, Anastassakis, Aris, Arbustini, Eloisa, Assanelli, Deodato, ...
Corrado, Domenico, Pelliccia, Antonio, Bjørnstad, Hans Halvor, Vanhees, Luc, Biffi, Alessandro, Borjesson, Mats, ...
The 1996 American Heart Association consensus panel recommendations stated that pre-participation cardiovascular screening for young competitive athletes is justifiable and compelling on ethical,...
Corrado, Domenico, Pelliccia, Antonio, Bjørnstad, Hans Halvor, Vanhees, Luc, Biffi, Alessandro, Borjesson, Mats, ...
The 1996 American Heart Association consensus panel recommendations stated that pre-participation cardiovascular screening for young competitive athletes is justifiable and compelling on ethical,...
Recommendations for competitive sports participation in athletes with cardiovascular disease (2005)
Pelliccia, Antonio, Fagard, Robert, Bjørnstad, Hans Halvor, Anastassakis, Aris, Arbustini, Eloisa, Assanelli, Deodato, ...
Tomé Esteban, María T., García-Pinilla, José M., McKenna, William J.
La miocardiopatía o displasia arritmogénica del ventrículo derecho (MAVD) es una enfermedad del músculo cardíaco de origen genético cuyo diagnóstico supone a menudo un reto para el clínico....
Basso, Cristina, Wichter, Thomas, Danieli, Gian A, Corrado, Domenico, Czarnowska, Elzbieta, Fontaine, Guy, ...
Natural history and familial characteristics of isolated left ventricular non-compaction (2004)
Murphy, Ross T., Thaman, Rajesh, Blanes, Juan Gimeno, Ward, Deirdre, Sevdalis, Elias, Papra, Efi, ...
Aims Non-compaction of the left ventricle (LVNC) is a disorder of endomyocardial morphogenesis that results in multiple trabeculations in the left ventricular myocardium. The current literature...
Moon, James C.C., Sachdev, Bhavesh, Elkington, Andrew G., McKenna, William J., Mehta, Atul, Pennell, Dudley J., ...
Aims Anderson-Fabry Disease (AFD), an X-linked disorder of sphingolipid metabolism, is a cause of idiopathic left ventricular hypertrophy but the mechanism of hypertrophy is poorly understood....
Update of the guidelines on sudden cardiac death of the European Society of Cardiology (2003)
Priori, Silvia G, Aliot, Etienne, Blomstrom-Lundqvist, Carina, Bossaert, Leo, Breithardt, Gunter, Brugada, Pedro, ...
Maron, Barry J., McKenna, William J., Danielson, Gordon K., Kappenberger, Lukas J., Kuhn, Horst J., ...
EROC: A Toolkit for Building NEATO Query Optimizers (1996)
William J. McKenna, Ol K. Ono, Raa Francois Raab, Tpc Benchmark D, P. Seshadri, ...
3] A. Chen, Y. F. Kao, M. Pong, D. Sak, S. Sharma, J. Vaishnav, and H. Zeller. Query processing in NonStop SQL. IEEE Data Eng. Bull., 16(4):29, December 1993. [CLR89] T. Cormen, C. Leiserson, and R....
Thesis (Ph. D.)--University of Colorado, 1993.
Nicklas, John M., McKenna, William J., Stewart, Ralph A., Mickelson, Judith K., Das, Sunil K., Schork, M. Anthony, ...
Sudden cardiac death is a common cause of mortality in patients with congestive heart failure. To determine if low-dose amiodarone could reduce sudden death among these patients, a prospective,...
Good Prognosis for Dilated Cardiomyopathy Without Severe Heart Failure or Arrhythmia (1990)
STEWART, RALPH A. H., MCKENNA, WILLIAM J., OAKLEY, CELIA M.
In 124 patients with dilated cardiomyopathy, symptoms of heart failure and ventricular arrhythmia at initial assessment were related to outcome a mean of 43 months later. Using life table analysis,...
'Pseudo' systolic anterior motion in patients with hypertensive heart disease (1983)
DOI, YOSHINORI L., MCKENNA, WILLIAM J., OAKLEY, CELIA M., GOODWIN, JOHN F.
The systolic motion of the mitral apparatus in patients with hypertensive heart disease and hypertrophic cardiomyopathy was studied in order to quantify the difference. Twelve out of 37 patients with...
Arad, Michael, Benson, D. Woodrow, Perez-Atayde, Antonio R., McKenna, William J., Sparks, Elizabeth A., Kanter, Ronald J., ...
Mutations in PRKAG2, the gene for the γ2 regulatory subunit of AMP-activated protein kinase, cause cardiac hypertrophy and electrophysiologic abnormalities, particularly preexcitation...
Mogensen, Jens, Kubo, Toru, Duque, Mauricio, Uribe, William, Shaw, Anthony, Murphy, Ross, ...
Restrictive cardiomyopathy (RCM) is an uncommon heart muscle disorder characterized by impaired filling of the ventricles with reduced volume in the presence of normal or near normal wall thickness...
Solomon, Scott D., Vosberg, Hans-Peter, Hiller, Gudrun, Jarcho, John A., Morton, Cynthia C., ...
We report that a gene responsible for familial hypertrophic cardiomyopathy (HC) is closely linked to the cardiac α and β myosin heavy chain (MHC) genes on chromosome 14q11. We have recently shown...
Syrris, Petros, Ward, Deirdre, Evans, Alison, Asimaki, Angeliki, Gandjbakhch, Estelle, Sen-Chowdhry, Srijita, ...
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited myocardial disorder associated with arrhythmias, heart failure, and sudden death. To date, mutations in four genes...
Keeling, Philip J, Jeffery, Stephen, Caforio, Alida L P, Taylor, Rohan, Bottazzo, Gian F, Davies, Michael J, ...
Objective—To assess the prevalence and significance of enteroviral genome within myocardial biopsy specimens taken from patients with idiopathic dilated cardiomyopathy and from controls.
Myocardial disarray in Noonan syndrome
Burch, Michael, Mann, Jessica M, Sharland, Michael, Shinebourne, Elliot A, Patton, Michael A, McKenna, William J
Objective—To characterise the histopathology of the left ventricular hypertrophy commonly associated with Noonan syndrome by assessing the extent of myocyte disarray and therefore to define one...