Jane E Crosson
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Explore the profile of Jane E Crosson including associated specialties, affiliations and a list of published articles.
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20
Citations
530
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Recent Articles
1.
Cadrin-Tourigny J, Bosman L, Nozza A, Wang W, Tadros R, Bhonsale A, et al.
Eur Heart J
. 2022 Apr;
43(32):e1-e9.
PMID: 35441664
Aims: Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC) is characterized by ventricular arrhythmias (VAs) and sudden cardiac death (SCD). We aimed to develop a model for individualized prediction of incident VA/SCD in...
2.
Cadrin-Tourigny J, Bosman L, Wang W, Tadros R, Bhonsale A, Bourfiss M, et al.
Circ Arrhythm Electrophysiol
. 2020 Dec;
14(1):e008509.
PMID: 33296238
Background: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is associated with ventricular arrhythmias (VA) and sudden cardiac death (SCD). A model was recently developed to predict incident sustained VA in patients with...
3.
Brown E, McMilllan K, Halushka M, Ravekes W, Knight M, Crosson J, et al.
Cardiol Young
. 2019 Jun;
29(7):917-921.
PMID: 31198128
There are a variety of causes of acute heart failure in children including myocarditis, genetic/metabolic conditions, and congenital heart defects. In cases with a structurally normal heart and a negative...
4.
Cadrin-Tourigny J, Bosman L, Nozza A, Wang W, Tadros R, Bhonsale A, et al.
Eur Heart J
. 2019 Mar;
40(23):1850-1858.
PMID: 30915475
Aims: Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC) is characterized by ventricular arrhythmias (VAs) and sudden cardiac death (SCD). We aimed to develop a model for individualized prediction of incident VA/SCD in...
5.
Mah D, Sleeper L, Crosson J, Czosek R, Love B, McCrindle B, et al.
Am J Cardiol
. 2018 Aug;
122(8):1429-1436.
PMID: 30115424
Patients with the Marfan syndrome (MFS) are at risk for sudden death. The contribution of arrhythmias is unclear. This study examines the prevalence of arrhythmias in children with the MFS...
6.
Orgeron G, Crosson J
Cardiol Young
. 2017 Jan;
27(S1):S57-S61.
PMID: 28084951
Arrhythmogenic right ventricular dysplasia/cardiomyopathy is an inherited cardiomyopathy characterised by ventricular arrhythmias and an increased risk of sudden cardiac death. Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnosis is based on criteria that...
7.
Crosson J, Nies M
Expert Rev Cardiovasc Ther
. 2015 Jan;
13(2):173-81.
PMID: 25583159
Brugada syndrome is an inherited arrhythmia associated with characteristic ST elevation in the right precordial leads and sudden cardiac death. The average age of sudden cardiac death is 40 years;...
8.
Ji S, Catanzaro J, Crosson J, Brinker J, Cheng A
Arch Med Sci
. 2014 Oct;
10(4):853-4.
PMID: 25276174
No abstract available.
9.
Perera J, Johnson N, Judge D, Crosson J
Pediatr Cardiol
. 2014 Jun;
35(7):1206-12.
PMID: 24880466
To date, several disease-related mutations in NKX2-5, a cardiac-specific homeobox gene, have been documented in patients with a variety of congenital heart diseases (CHDs). The most commonly reported phenotypes are...
10.
Crosson J, Callans D, Bradley D, Dubin A, Epstein M, Etheridge S, et al.
Heart Rhythm
. 2014 May;
11(9):e55-78.
PMID: 24814375
No abstract available.