William J McKenna
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Explore the profile of William J McKenna including associated specialties, affiliations and a list of published articles.
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241
Citations
15108
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Recent Articles
1.
Protonotarios A, Asimaki A, Basso C, Xylouri Z, Monda E, Protonotarios I, et al.
JACC Adv
. 2025 Jan;
4(2):101547.
PMID: 39877668
Naxos disease is a rare autosomal recessive condition combining arrhythmogenic right ventricular cardiomyopathy, woolly hair, and palmoplantar keratoderma. The first identified causative variant was in the gene encoding the desmosomal...
2.
McKenna W, Asch F, Coats C, Garcia-Hernandez S, Sonicheva-Paterson N, Solomon S
J Am Coll Cardiol
. 2025 Jan;
85(7):696-698.
PMID: 39772356
No abstract available.
3.
Tsatsopoulou A, Garcia-Hernandez S, McKenna W
Eur Heart J
. 2024 Dec;
46(4):377-379.
PMID: 39656820
No abstract available.
4.
Cabrera-Borrego E, Bermudez-Jimenez F, Gasperetti A, Tandri H, Sanchez-Millan P, Molina-Lerma M, et al.
Circ Arrhythm Electrophysiol
. 2024 Nov;
17(12):e013145.
PMID: 39611258
Background: Among inherited cardiomyopathies involving the left ventricle, whether dilated or not, certain genotypes carry a well-established arrhythmic risk, notably manifested as sustained monomorphic ventricular tachycardia (SMVT). Nonetheless, the precise...
5.
Anastasiou V, Papazoglou A, Gossios T, Zegkos T, Daios S, Moysidis D, et al.
Eur J Heart Fail
. 2024 Jul;
26(10):2155-2168.
PMID: 39078390
Aims: Evidence on the relative impact of diverse genetic backgrounds associated with non-ischaemic dilated cardiomyopathy (DCM) remains contradictory. This study sought to synthesize the available data regarding long-term outcomes of...
6.
Bermudez-Jimenez F, Protonotarios A, Garcia-Hernandez S, Perez Asensio A, Rampazzo A, Zorio E, et al.
JACC Clin Electrophysiol
. 2024 May;
10(6):1178-1190.
PMID: 38727660
Background: Desmin (DES) pathogenic variants cause a small proportion of arrhythmogenic cardiomyopathy (ACM). Outcomes data on DES-related ACM are scarce. Objectives: This study sought to provide information on the clinical...
7.
McKenna W, Crean A, Greenway S, Tadros R, Veselka J, Woo A
Can J Cardiol
. 2024 Mar;
40(5):738-741.
PMID: 38492736
No abstract available.
8.
Garcia-Hernandez S, de la Higuera Romero L, Ochoa J, McKenna W
Can J Cardiol
. 2024 Jan;
40(5):742-753.
PMID: 38244984
Hypertrophic cardiomyopathy (HCM), defined clinically by the presence of unexplained left ventricular hypertrophy (LVH), with wall thickness ≥ 1.5 cm, is a phenotype in search of a diagnosis, which is...
9.
Proposed diagnostic criteria for arrhythmogenic cardiomyopathy: European Task Force consensus report
Corrado D, Anastasakis A, Basso C, Bauce B, Blomstrom-Lundqvist C, Bucciarelli-Ducci C, et al.
Int J Cardiol
. 2023 Oct;
395:131447.
PMID: 37844667
Arrhythmogenic cardiomyopathy (ACM) is a heart muscle disease characterized by prominent "non-ischemic" myocardial scarring predisposing to ventricular electrical instability. Diagnostic criteria for the original phenotype, arrhythmogenic right ventricular cardiomyopathy (ARVC),...
10.
Gandaeva L, Sonicheva-Paterson N, McKenna W, Savostyanov K, Myasnikov R, Pushkov A, et al.
Int J Cardiol
. 2023 Jul;
389:131189.
PMID: 37454822
Successful therapy in a cohort with early onset Danon disease (DD) highlights the potential importance of earlier disease recognition. We present experience from the largest National Pediatric Center in Russia...