Arrhythmogenic cardiomyopathy (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Arrhythmogenic cardiomyopathy" in English language version.

refsWebsite

Global rank English rank

56nih.gov

4^th place

40doi.org

2^nd place

7semanticscholar.org

11^th place

8^th place

5handle.net

102^nd place

76^th place

3web.archive.org

1^st place

2dispatch.com

1,969^th place

1,098^th place

2bbc.co.uk

8^th place

10^th place

1oup.com

485^th place

440^th place

1ucl.ac.uk

1,306^th place

885^th place

1harvard.edu

18^th place

17^th place

1hypothesisjournal.com

low place

1cnn.com

28^th place

26^th place

1cidg.org

low place

1icnetwork.co.uk

5,909^th place

3,682^nd place

1msn.com

117^th place

145^th place

1youtube.com

9^th place

13^th place

bbc.co.uk

news.bbc.co.uk

"Sevilla star suffers heart attack". BBC Sport. 2007-08-25. Retrieved 2007-08-25.

bbc.co.uk

"James Taylor: England & Nottinghamshire batsman forced to retire". BBC Sport. 2016-04-12. Retrieved 2016-05-15.

cidg.org

"Cause of Death". Cardiac Inherited Disease Group. Archived from the original on 2006-08-18. Retrieved 2006-10-31.

cnn.com

edition.cnn.com

"Sevilla star dies after collapse - CNN.com". edition.cnn.com.

dispatch.com

Jardy A. "Crew midfielder Kirk Urso, 22, dies after being rushed to hospital from bar". The Columbus Dispatch. The Dispatch Printing Company. Archived from the original on 17 October 2012. Retrieved 21 September 2012.
Jardy A. "Coroner: Crew's Urso died of a preexisting heart condition". The Columbus Dispatch. The Dispatch Printing Company. Archived from the original on 24 September 2012. Retrieved 21 September 2012.

doi.org

Pilichou K, Thiene G, Bauce B, Rigato I, Lazzarini E, Migliore F, et al. (April 2016). "Arrhythmogenic cardiomyopathy". Orphanet Journal of Rare Diseases. 11 (1): 33. doi:10.1186/s13023-016-0407-1. PMC 4818879. PMID 27038780.
Heidbuchel H, Prior DL, La Gerche A (November 2012). "Ventricular arrhythmias associated with long-term endurance sports: what is the evidence?". British Journal of Sports Medicine. 46 (Suppl 1): i44–i50. doi:10.1136/bjsports-2012-091162. PMID 23097479. S2CID 41256939.
Corrado D, Basso C, Judge DP (September 2017). "Arrhythmogenic Cardiomyopathy". Circulation Research. 121 (7): 784–802. doi:10.1161/CIRCRESAHA.117.309345. PMC 4818879. PMID 28912183.
Corrado D, Link MS, Calkins H (January 2017). "Arrhythmogenic Right Ventricular Cardiomyopathy". The New England Journal of Medicine. 376 (1): 61–72. doi:10.1056/NEJMra1509267. PMID 28052233. S2CID 7754633.
Cox MG, van der Zwaag PA, van der Werf C, van der Smagt JJ, Noorman M, Bhuiyan ZA, et al. (June 2011). "Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study". Circulation. 123 (23): 2690–2700. doi:10.1161/circulationaha.110.988287. PMID 21606396.
Fressart V, Duthoit G, Donal E, Probst V, Deharo JC, Chevalier P, et al. (June 2010). "Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice". Europace. 12 (6): 861–868. doi:10.1093/europace/euq104. PMID 20400443.
Klauke B, Kossmann S, Gaertner A, Brand K, Stork I, Brodehl A, et al. (December 2010). "De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy". Human Molecular Genetics. 19 (23): 4595–4607. doi:10.1093/hmg/ddq387. PMID 20829228.
Brodehl A, Hedde PN, Dieding M, Fatima A, Walhorn V, Gayda S, et al. (May 2012). "Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants". The Journal of Biological Chemistry. 287 (19): 16047–16057. doi:10.1074/jbc.M111.313841. PMC 3346104. PMID 22403400.
Beffagna G, Occhi G, Nava A, Vitiello L, Ditadi A, Basso C, et al. (February 2005). "Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1". Cardiovascular Research. 65 (2): 366–373. doi:10.1016/j.cardiores.2004.10.005. PMID 15639475.
Milting H, Lukas N, Klauke B, Körfer R, Perrot A, Osterziel KJ, et al. (August 2006). "Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy". Cardiovascular Research. 71 (3): 496–505. doi:10.1016/j.cardiores.2006.04.004. PMID 16769042.
Severini GM, Krajinovic M, Pinamonti B, Sinagra G, Fioretti P, Brunazzi MC, et al. (January 1996). "A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14". Genomics. 31 (2): 193–200. doi:10.1006/geno.1996.0031. hdl:1765/58364. PMID 8824801.
Rampazzo A, Nava A, Miorin M, Fonderico P, Pope B, Tiso N, et al. (October 1997). "ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm". Genomics. 45 (2): 259–263. doi:10.1006/geno.1997.4927. hdl:11577/2461314. PMID 9344647.
Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, et al. (April 2008). "Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene". American Journal of Human Genetics. 82 (4): 809–821. doi:10.1016/j.ajhg.2008.01.010. PMC 2427209. PMID 18313022.
Christensen AH, Andersen CB, Tybjaerg-Hansen A, Haunso S, Svendsen JH (September 2011). "Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy". Clinical Genetics. 80 (3): 256–264. doi:10.1111/j.1399-0004.2011.01623.x. PMID 21214875. S2CID 5617616.
Li D, Ahmad F, Gardner MJ, Weilbaecher D, Hill R, Karibe A, et al. (January 2000). "The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14". American Journal of Human Genetics. 66 (1): 148–156. doi:10.1086/302713. PMC 1288320. PMID 10631146.
Protonotarios A, Brodehl A, Asimaki A, Jager J, Quinn E, Stanasiuk C, et al. (June 2021). "The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy". The Canadian Journal of Cardiology. 37 (6): 857–866. doi:10.1016/j.cjca.2020.11.017. PMID 33290826. S2CID 228078648.
Bermúdez-Jiménez FJ, Carriel V, Brodehl A, Alaminos M, Campos A, Schirmer I, et al. (April 2018). "Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia". Circulation. 137 (15): 1595–1610. doi:10.1161/CIRCULATIONAHA.117.028719. hdl:10481/89514. PMID 29212896.
Bauce B, Basso C, Rampazzo A, Beffagna G, Daliento L, Frigo G, et al. (August 2005). "Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations". European Heart Journal. 26 (16): 1666–1675. doi:10.1093/eurheartj/ehi341. PMID 15941723.
Gerull B, Heuser A, Wichter T, Paul M, Basson CT, McDermott DA, et al. (November 2004). "Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy". Nature Genetics. 36 (11): 1162–1164. doi:10.1038/ng1461. PMID 15489853.
Pilichou K, Nava A, Basso C, Beffagna G, Bauce B, Lorenzon A, et al. (March 2006). "Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy". Circulation. 113 (9): 1171–1179. doi:10.1161/CIRCULATIONAHA.105.583674. hdl:11577/2434417. PMID 16505173.
Awad MM, Dalal D, Cho E, Amat-Alarcon N, James C, Tichnell C, et al. (July 2006). "DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy". American Journal of Human Genetics. 79 (1): 136–142. doi:10.1086/504393. PMC 1474134. PMID 16773573.
Brodehl A, Meshkov A, Myasnikov R, Kiseleva A, Kulikova O, Klauke B, et al. (April 2021). "Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset". International Journal of Molecular Sciences. 22 (7): 3786. doi:10.3390/ijms22073786. PMC 8038858. PMID 33917638.
Brodehl A, Weiss J, Debus JD, Stanasiuk C, Klauke B, Deutsch MA, et al. (April 2020). "A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy". Journal of Molecular and Cellular Cardiology. 141: 17–29. doi:10.1016/j.yjmcc.2020.03.006. PMID 32201174.
Heuser A, Plovie ER, Ellinor PT, Grossmann KS, Shin JT, Wichter T, et al. (December 2006). "Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy". American Journal of Human Genetics. 79 (6): 1081–1088. doi:10.1086/509044. PMC 1698714. PMID 17186466.
Syrris P, Ward D, Evans A, Asimaki A, Gandjbakhch E, Sen-Chowdhry S, et al. (November 2006). "Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2". American Journal of Human Genetics. 79 (5): 978–984. doi:10.1086/509122. PMC 1698574. PMID 17033975.
Antoniades L, Tsatsopoulou A, Anastasakis A, Syrris P, Asimaki A, Panagiotakos D, et al. (September 2006). "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". European Heart Journal. 27 (18): 2208–2216. doi:10.1093/eurheartj/ehl184. PMID 16893920.
Asimaki A, Syrris P, Wichter T, Matthias P, Saffitz JE, McKenna WJ (November 2007). "A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy". American Journal of Human Genetics. 81 (5): 964–973. doi:10.1086/521633. PMC 2265660. PMID 17924338.
Brodehl A, Rezazadeh S, Williams T, Munsie NM, Liedtke D, Oh T, et al. (June 2019). "Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy". Translational Research. 208: 15–29. doi:10.1016/j.trsl.2019.02.004. PMC 7412573. PMID 30802431.
Forleo C, Carmosino M, Resta N, Rampazzo A, Valecce R, Sorrentino S, et al. (2015). "Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy". PLOS ONE. 10 (4): e0121723. Bibcode:2015PLoSO..1021723F. doi:10.1371/journal.pone.0121723. PMC 4383583. PMID 25837155.
La Gerche A (January 2021). "Exercise-Induced Arrhythmogenic (Right Ventricular) Cardiomyopathy Is Real…if you Consider it". JACC. Cardiovascular Imaging. 14 (1): 159–161. doi:10.1016/j.jcmg.2020.09.014. PMID 33221208.
Prior D, La Gerche A (April 2020). "Exercise and Arrhythmogenic Right Ventricular Cardiomyopathy". Heart, Lung & Circulation. 29 (4): 547–555. doi:10.1016/j.hlc.2019.12.007. PMID 31964580.
Heidbüchel H, La Gerche A (June 2012). "The right heart in athletes. Evidence for exercise-induced arrhythmogenic right ventricular cardiomyopathy". Herzschrittmachertherapie & Elektrophysiologie. 23 (2): 82–86. doi:10.1007/s00399-012-0180-3. PMID 22782727. S2CID 192598349.
La Gerche A, Heidbüchel H, Burns AT, Mooney DJ, Taylor AJ, Pfluger HB, et al. (June 2011). "Disproportionate exercise load and remodeling of the athlete's right ventricle". Medicine and Science in Sports and Exercise. 43 (6): 974–981. doi:10.1249/MSS.0b013e31820607a3. PMID 21085033.
Darden D, Scheinman MM, Hoffmayer KS (September 2022). "Exercise-induced arrhythmogenic right ventricular cardiomyopathy: Reverse remodeling with detraining". HeartRhythm Case Reports. 8 (9): 599–603. doi:10.1016/j.hrcr.2022.06.003. PMC 9485656. PMID 36147714. S2CID 249838976.
Mazzanti A, Ng K, Faragli A, Maragna R, Chiodaroli E, Orphanou N, et al. (December 2016). "Arrhythmogenic Right Ventricular Cardiomyopathy: Clinical Course and Predictors of Arrhythmic Risk". Journal of the American College of Cardiology. 68 (23): 2540–2550. doi:10.1016/j.jacc.2016.09.951. PMID 27931611.
Sen-Chowdhry S, Syrris P, McKenna WJ (November 2007). "Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy". Journal of the American College of Cardiology. 50 (19): 1813–1821. doi:10.1016/j.jacc.2007.08.008. PMID 17980246.
Marcus FI, McKenna WJ, Sherrill D, Basso C, Bauce B, Bluemke DA, et al. (April 2010). "Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria". Circulation. 121 (13): 1533–1541. doi:10.1161/CIRCULATIONAHA.108.840827. PMC 2860804. PMID 20172911.
Pelliccia A, Solberg EE, Papadakis M, Adami PE, Biffi A, Caselli S, et al. (January 2019). "Recommendations for participation in competitive and leisure time sport in athletes with cardiomyopathies, myocarditis, and pericarditis: position statement of the Sport Cardiology Section of the European Association of Preventive Cardiology (EAPC)". European Heart Journal. 40 (1): 19–33. doi:10.1093/eurheartj/ehy730. hdl:2158/1180375. PMID 30561613.
Fontaine G, Tonet J, Gallais Y, Lascault G, Hidden-Lucet F, Aouate P, et al. (November 2000). "Ventricular tachycardia catheter ablation in arrhythmogenic right ventricular dysplasia: a 16-year experience". Current Cardiology Reports. 2 (6): 498–506. doi:10.1007/s11886-000-0034-1. PMID 11203287. S2CID 31406061.
Lahtinen AM, Lehtonen E, Marjamaa A, Kaartinen M, Heliö T, Porthan K, et al. (August 2011). "Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy". Heart Rhythm. 8 (8): 1214–1221. doi:10.1016/j.hrthm.2011.03.015. PMID 21397041.

handle.net

hdl.handle.net

Severini GM, Krajinovic M, Pinamonti B, Sinagra G, Fioretti P, Brunazzi MC, et al. (January 1996). "A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14". Genomics. 31 (2): 193–200. doi:10.1006/geno.1996.0031. hdl:1765/58364. PMID 8824801.
Rampazzo A, Nava A, Miorin M, Fonderico P, Pope B, Tiso N, et al. (October 1997). "ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm". Genomics. 45 (2): 259–263. doi:10.1006/geno.1997.4927. hdl:11577/2461314. PMID 9344647.
Bermúdez-Jiménez FJ, Carriel V, Brodehl A, Alaminos M, Campos A, Schirmer I, et al. (April 2018). "Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia". Circulation. 137 (15): 1595–1610. doi:10.1161/CIRCULATIONAHA.117.028719. hdl:10481/89514. PMID 29212896.
Pilichou K, Nava A, Basso C, Beffagna G, Bauce B, Lorenzon A, et al. (March 2006). "Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy". Circulation. 113 (9): 1171–1179. doi:10.1161/CIRCULATIONAHA.105.583674. hdl:11577/2434417. PMID 16505173.
Pelliccia A, Solberg EE, Papadakis M, Adami PE, Biffi A, Caselli S, et al. (January 2019). "Recommendations for participation in competitive and leisure time sport in athletes with cardiomyopathies, myocarditis, and pericarditis: position statement of the Sport Cardiology Section of the European Association of Preventive Cardiology (EAPC)". European Heart Journal. 40 (1): 19–33. doi:10.1093/eurheartj/ehy730. hdl:2158/1180375. PMID 30561613.

harvard.edu

ui.adsabs.harvard.edu

Forleo C, Carmosino M, Resta N, Rampazzo A, Valecce R, Sorrentino S, et al. (2015). "Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy". PLOS ONE. 10 (4): e0121723. Bibcode:2015PLoSO..1021723F. doi:10.1371/journal.pone.0121723. PMC 4383583. PMID 25837155.

hypothesisjournal.com

Jain R. Athletic status and arrhythmogenic right ventricular dysplasia/cardiomyopathy: From physiological observations to pathological explanation. Hypothesis 2010, 8(1): e2. – See more at: http://www.hypothesisjournal.com/?p=844#sthash.aB859Jm2.dpuf

icnetwork.co.uk

icbirmingham.icnetwork.co.uk

"Shock at star player's death". icBirmingham.co.uk. 11 September 2006. Retrieved 2007-11-26.

msn.com

Suzanne Crough died of rare heart ailment, coroner says, msn.com; accessed October 27, 2015.

nih.gov

pubmed.ncbi.nlm.nih.gov

Pilichou K, Thiene G, Bauce B, Rigato I, Lazzarini E, Migliore F, et al. (April 2016). "Arrhythmogenic cardiomyopathy". Orphanet Journal of Rare Diseases. 11 (1): 33. doi:10.1186/s13023-016-0407-1. PMC 4818879. PMID 27038780.
Heidbuchel H, Prior DL, La Gerche A (November 2012). "Ventricular arrhythmias associated with long-term endurance sports: what is the evidence?". British Journal of Sports Medicine. 46 (Suppl 1): i44–i50. doi:10.1136/bjsports-2012-091162. PMID 23097479. S2CID 41256939.
Corrado D, Basso C, Judge DP (September 2017). "Arrhythmogenic Cardiomyopathy". Circulation Research. 121 (7): 784–802. doi:10.1161/CIRCRESAHA.117.309345. PMC 4818879. PMID 28912183.
Corrado D, Link MS, Calkins H (January 2017). "Arrhythmogenic Right Ventricular Cardiomyopathy". The New England Journal of Medicine. 376 (1): 61–72. doi:10.1056/NEJMra1509267. PMID 28052233. S2CID 7754633.
Cox MG, van der Zwaag PA, van der Werf C, van der Smagt JJ, Noorman M, Bhuiyan ZA, et al. (June 2011). "Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study". Circulation. 123 (23): 2690–2700. doi:10.1161/circulationaha.110.988287. PMID 21606396.
Fressart V, Duthoit G, Donal E, Probst V, Deharo JC, Chevalier P, et al. (June 2010). "Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice". Europace. 12 (6): 861–868. doi:10.1093/europace/euq104. PMID 20400443.
Klauke B, Kossmann S, Gaertner A, Brand K, Stork I, Brodehl A, et al. (December 2010). "De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy". Human Molecular Genetics. 19 (23): 4595–4607. doi:10.1093/hmg/ddq387. PMID 20829228.
Brodehl A, Hedde PN, Dieding M, Fatima A, Walhorn V, Gayda S, et al. (May 2012). "Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants". The Journal of Biological Chemistry. 287 (19): 16047–16057. doi:10.1074/jbc.M111.313841. PMC 3346104. PMID 22403400.
Beffagna G, Occhi G, Nava A, Vitiello L, Ditadi A, Basso C, et al. (February 2005). "Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1". Cardiovascular Research. 65 (2): 366–373. doi:10.1016/j.cardiores.2004.10.005. PMID 15639475.
Milting H, Lukas N, Klauke B, Körfer R, Perrot A, Osterziel KJ, et al. (August 2006). "Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy". Cardiovascular Research. 71 (3): 496–505. doi:10.1016/j.cardiores.2006.04.004. PMID 16769042.
Severini GM, Krajinovic M, Pinamonti B, Sinagra G, Fioretti P, Brunazzi MC, et al. (January 1996). "A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14". Genomics. 31 (2): 193–200. doi:10.1006/geno.1996.0031. hdl:1765/58364. PMID 8824801.
Rampazzo A, Nava A, Miorin M, Fonderico P, Pope B, Tiso N, et al. (October 1997). "ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm". Genomics. 45 (2): 259–263. doi:10.1006/geno.1997.4927. hdl:11577/2461314. PMID 9344647.
Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, et al. (April 2008). "Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene". American Journal of Human Genetics. 82 (4): 809–821. doi:10.1016/j.ajhg.2008.01.010. PMC 2427209. PMID 18313022.
Christensen AH, Andersen CB, Tybjaerg-Hansen A, Haunso S, Svendsen JH (September 2011). "Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy". Clinical Genetics. 80 (3): 256–264. doi:10.1111/j.1399-0004.2011.01623.x. PMID 21214875. S2CID 5617616.
Li D, Ahmad F, Gardner MJ, Weilbaecher D, Hill R, Karibe A, et al. (January 2000). "The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14". American Journal of Human Genetics. 66 (1): 148–156. doi:10.1086/302713. PMC 1288320. PMID 10631146.
Protonotarios A, Brodehl A, Asimaki A, Jager J, Quinn E, Stanasiuk C, et al. (June 2021). "The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy". The Canadian Journal of Cardiology. 37 (6): 857–866. doi:10.1016/j.cjca.2020.11.017. PMID 33290826. S2CID 228078648.
Bermúdez-Jiménez FJ, Carriel V, Brodehl A, Alaminos M, Campos A, Schirmer I, et al. (April 2018). "Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia". Circulation. 137 (15): 1595–1610. doi:10.1161/CIRCULATIONAHA.117.028719. hdl:10481/89514. PMID 29212896.
Bauce B, Basso C, Rampazzo A, Beffagna G, Daliento L, Frigo G, et al. (August 2005). "Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations". European Heart Journal. 26 (16): 1666–1675. doi:10.1093/eurheartj/ehi341. PMID 15941723.
Gerull B, Heuser A, Wichter T, Paul M, Basson CT, McDermott DA, et al. (November 2004). "Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy". Nature Genetics. 36 (11): 1162–1164. doi:10.1038/ng1461. PMID 15489853.
Pilichou K, Nava A, Basso C, Beffagna G, Bauce B, Lorenzon A, et al. (March 2006). "Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy". Circulation. 113 (9): 1171–1179. doi:10.1161/CIRCULATIONAHA.105.583674. hdl:11577/2434417. PMID 16505173.
Awad MM, Dalal D, Cho E, Amat-Alarcon N, James C, Tichnell C, et al. (July 2006). "DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy". American Journal of Human Genetics. 79 (1): 136–142. doi:10.1086/504393. PMC 1474134. PMID 16773573.
Brodehl A, Meshkov A, Myasnikov R, Kiseleva A, Kulikova O, Klauke B, et al. (April 2021). "Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset". International Journal of Molecular Sciences. 22 (7): 3786. doi:10.3390/ijms22073786. PMC 8038858. PMID 33917638.
Brodehl A, Weiss J, Debus JD, Stanasiuk C, Klauke B, Deutsch MA, et al. (April 2020). "A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy". Journal of Molecular and Cellular Cardiology. 141: 17–29. doi:10.1016/j.yjmcc.2020.03.006. PMID 32201174.
Heuser A, Plovie ER, Ellinor PT, Grossmann KS, Shin JT, Wichter T, et al. (December 2006). "Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy". American Journal of Human Genetics. 79 (6): 1081–1088. doi:10.1086/509044. PMC 1698714. PMID 17186466.
Syrris P, Ward D, Evans A, Asimaki A, Gandjbakhch E, Sen-Chowdhry S, et al. (November 2006). "Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2". American Journal of Human Genetics. 79 (5): 978–984. doi:10.1086/509122. PMC 1698574. PMID 17033975.
Antoniades L, Tsatsopoulou A, Anastasakis A, Syrris P, Asimaki A, Panagiotakos D, et al. (September 2006). "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". European Heart Journal. 27 (18): 2208–2216. doi:10.1093/eurheartj/ehl184. PMID 16893920.
Asimaki A, Syrris P, Wichter T, Matthias P, Saffitz JE, McKenna WJ (November 2007). "A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy". American Journal of Human Genetics. 81 (5): 964–973. doi:10.1086/521633. PMC 2265660. PMID 17924338.
Brodehl A, Rezazadeh S, Williams T, Munsie NM, Liedtke D, Oh T, et al. (June 2019). "Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy". Translational Research. 208: 15–29. doi:10.1016/j.trsl.2019.02.004. PMC 7412573. PMID 30802431.
Forleo C, Carmosino M, Resta N, Rampazzo A, Valecce R, Sorrentino S, et al. (2015). "Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy". PLOS ONE. 10 (4): e0121723. Bibcode:2015PLoSO..1021723F. doi:10.1371/journal.pone.0121723. PMC 4383583. PMID 25837155.
La Gerche A (January 2021). "Exercise-Induced Arrhythmogenic (Right Ventricular) Cardiomyopathy Is Real…if you Consider it". JACC. Cardiovascular Imaging. 14 (1): 159–161. doi:10.1016/j.jcmg.2020.09.014. PMID 33221208.
Prior D, La Gerche A (April 2020). "Exercise and Arrhythmogenic Right Ventricular Cardiomyopathy". Heart, Lung & Circulation. 29 (4): 547–555. doi:10.1016/j.hlc.2019.12.007. PMID 31964580.
Heidbüchel H, La Gerche A (June 2012). "The right heart in athletes. Evidence for exercise-induced arrhythmogenic right ventricular cardiomyopathy". Herzschrittmachertherapie & Elektrophysiologie. 23 (2): 82–86. doi:10.1007/s00399-012-0180-3. PMID 22782727. S2CID 192598349.
La Gerche A, Heidbüchel H, Burns AT, Mooney DJ, Taylor AJ, Pfluger HB, et al. (June 2011). "Disproportionate exercise load and remodeling of the athlete's right ventricle". Medicine and Science in Sports and Exercise. 43 (6): 974–981. doi:10.1249/MSS.0b013e31820607a3. PMID 21085033.
Darden D, Scheinman MM, Hoffmayer KS (September 2022). "Exercise-induced arrhythmogenic right ventricular cardiomyopathy: Reverse remodeling with detraining". HeartRhythm Case Reports. 8 (9): 599–603. doi:10.1016/j.hrcr.2022.06.003. PMC 9485656. PMID 36147714. S2CID 249838976.
Mazzanti A, Ng K, Faragli A, Maragna R, Chiodaroli E, Orphanou N, et al. (December 2016). "Arrhythmogenic Right Ventricular Cardiomyopathy: Clinical Course and Predictors of Arrhythmic Risk". Journal of the American College of Cardiology. 68 (23): 2540–2550. doi:10.1016/j.jacc.2016.09.951. PMID 27931611.
Sen-Chowdhry S, Syrris P, McKenna WJ (November 2007). "Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy". Journal of the American College of Cardiology. 50 (19): 1813–1821. doi:10.1016/j.jacc.2007.08.008. PMID 17980246.
McNally E, MacLeod H, Dellefave-Castillo L (11 May 2023). "Arrhythmogenic Right Ventricular Cardiomyopathy Overview". In Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LH, Gripp KW, Amemiya A (eds.). GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle. PMID 20301310.
Marcus FI, McKenna WJ, Sherrill D, Basso C, Bauce B, Bluemke DA, et al. (April 2010). "Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria". Circulation. 121 (13): 1533–1541. doi:10.1161/CIRCULATIONAHA.108.840827. PMC 2860804. PMID 20172911.
Pelliccia A, Solberg EE, Papadakis M, Adami PE, Biffi A, Caselli S, et al. (January 2019). "Recommendations for participation in competitive and leisure time sport in athletes with cardiomyopathies, myocarditis, and pericarditis: position statement of the Sport Cardiology Section of the European Association of Preventive Cardiology (EAPC)". European Heart Journal. 40 (1): 19–33. doi:10.1093/eurheartj/ehy730. hdl:2158/1180375. PMID 30561613.
Fontaine G, Tonet J, Gallais Y, Lascault G, Hidden-Lucet F, Aouate P, et al. (November 2000). "Ventricular tachycardia catheter ablation in arrhythmogenic right ventricular dysplasia: a 16-year experience". Current Cardiology Reports. 2 (6): 498–506. doi:10.1007/s11886-000-0034-1. PMID 11203287. S2CID 31406061.
Lahtinen AM, Lehtonen E, Marjamaa A, Kaartinen M, Heliö T, Porthan K, et al. (August 2011). "Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy". Heart Rhythm. 8 (8): 1214–1221. doi:10.1016/j.hrthm.2011.03.015. PMID 21397041.

ncbi.nlm.nih.gov

Pilichou K, Thiene G, Bauce B, Rigato I, Lazzarini E, Migliore F, et al. (April 2016). "Arrhythmogenic cardiomyopathy". Orphanet Journal of Rare Diseases. 11 (1): 33. doi:10.1186/s13023-016-0407-1. PMC 4818879. PMID 27038780.
Corrado D, Basso C, Judge DP (September 2017). "Arrhythmogenic Cardiomyopathy". Circulation Research. 121 (7): 784–802. doi:10.1161/CIRCRESAHA.117.309345. PMC 4818879. PMID 28912183.
Brodehl A, Hedde PN, Dieding M, Fatima A, Walhorn V, Gayda S, et al. (May 2012). "Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants". The Journal of Biological Chemistry. 287 (19): 16047–16057. doi:10.1074/jbc.M111.313841. PMC 3346104. PMID 22403400.
Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, et al. (April 2008). "Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene". American Journal of Human Genetics. 82 (4): 809–821. doi:10.1016/j.ajhg.2008.01.010. PMC 2427209. PMID 18313022.
Li D, Ahmad F, Gardner MJ, Weilbaecher D, Hill R, Karibe A, et al. (January 2000). "The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14". American Journal of Human Genetics. 66 (1): 148–156. doi:10.1086/302713. PMC 1288320. PMID 10631146.
Awad MM, Dalal D, Cho E, Amat-Alarcon N, James C, Tichnell C, et al. (July 2006). "DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy". American Journal of Human Genetics. 79 (1): 136–142. doi:10.1086/504393. PMC 1474134. PMID 16773573.
Brodehl A, Meshkov A, Myasnikov R, Kiseleva A, Kulikova O, Klauke B, et al. (April 2021). "Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset". International Journal of Molecular Sciences. 22 (7): 3786. doi:10.3390/ijms22073786. PMC 8038858. PMID 33917638.
Heuser A, Plovie ER, Ellinor PT, Grossmann KS, Shin JT, Wichter T, et al. (December 2006). "Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy". American Journal of Human Genetics. 79 (6): 1081–1088. doi:10.1086/509044. PMC 1698714. PMID 17186466.
Syrris P, Ward D, Evans A, Asimaki A, Gandjbakhch E, Sen-Chowdhry S, et al. (November 2006). "Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2". American Journal of Human Genetics. 79 (5): 978–984. doi:10.1086/509122. PMC 1698574. PMID 17033975.
Asimaki A, Syrris P, Wichter T, Matthias P, Saffitz JE, McKenna WJ (November 2007). "A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy". American Journal of Human Genetics. 81 (5): 964–973. doi:10.1086/521633. PMC 2265660. PMID 17924338.
Brodehl A, Rezazadeh S, Williams T, Munsie NM, Liedtke D, Oh T, et al. (June 2019). "Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy". Translational Research. 208: 15–29. doi:10.1016/j.trsl.2019.02.004. PMC 7412573. PMID 30802431.
Forleo C, Carmosino M, Resta N, Rampazzo A, Valecce R, Sorrentino S, et al. (2015). "Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy". PLOS ONE. 10 (4): e0121723. Bibcode:2015PLoSO..1021723F. doi:10.1371/journal.pone.0121723. PMC 4383583. PMID 25837155.
Darden D, Scheinman MM, Hoffmayer KS (September 2022). "Exercise-induced arrhythmogenic right ventricular cardiomyopathy: Reverse remodeling with detraining". HeartRhythm Case Reports. 8 (9): 599–603. doi:10.1016/j.hrcr.2022.06.003. PMC 9485656. PMID 36147714. S2CID 249838976.
McNally E, MacLeod H, Dellefave-Castillo L (11 May 2023). "Arrhythmogenic Right Ventricular Cardiomyopathy Overview". In Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LH, Gripp KW, Amemiya A (eds.). GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle. PMID 20301310.
Marcus FI, McKenna WJ, Sherrill D, Basso C, Bauce B, Bluemke DA, et al. (April 2010). "Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria". Circulation. 121 (13): 1533–1541. doi:10.1161/CIRCULATIONAHA.108.840827. PMC 2860804. PMID 20172911.

oup.com

academic.oup.com

"Exercise-induced arrhythmogenic right ventricular cardiomyopathy: fact or fallacy?". 2011. Retrieved 2022-02-18.

semanticscholar.org

api.semanticscholar.org

Heidbuchel H, Prior DL, La Gerche A (November 2012). "Ventricular arrhythmias associated with long-term endurance sports: what is the evidence?". British Journal of Sports Medicine. 46 (Suppl 1): i44–i50. doi:10.1136/bjsports-2012-091162. PMID 23097479. S2CID 41256939.
Corrado D, Link MS, Calkins H (January 2017). "Arrhythmogenic Right Ventricular Cardiomyopathy". The New England Journal of Medicine. 376 (1): 61–72. doi:10.1056/NEJMra1509267. PMID 28052233. S2CID 7754633.
Christensen AH, Andersen CB, Tybjaerg-Hansen A, Haunso S, Svendsen JH (September 2011). "Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy". Clinical Genetics. 80 (3): 256–264. doi:10.1111/j.1399-0004.2011.01623.x. PMID 21214875. S2CID 5617616.
Protonotarios A, Brodehl A, Asimaki A, Jager J, Quinn E, Stanasiuk C, et al. (June 2021). "The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy". The Canadian Journal of Cardiology. 37 (6): 857–866. doi:10.1016/j.cjca.2020.11.017. PMID 33290826. S2CID 228078648.
Heidbüchel H, La Gerche A (June 2012). "The right heart in athletes. Evidence for exercise-induced arrhythmogenic right ventricular cardiomyopathy". Herzschrittmachertherapie & Elektrophysiologie. 23 (2): 82–86. doi:10.1007/s00399-012-0180-3. PMID 22782727. S2CID 192598349.
Darden D, Scheinman MM, Hoffmayer KS (September 2022). "Exercise-induced arrhythmogenic right ventricular cardiomyopathy: Reverse remodeling with detraining". HeartRhythm Case Reports. 8 (9): 599–603. doi:10.1016/j.hrcr.2022.06.003. PMC 9485656. PMID 36147714. S2CID 249838976.
Fontaine G, Tonet J, Gallais Y, Lascault G, Hidden-Lucet F, Aouate P, et al. (November 2000). "Ventricular tachycardia catheter ablation in arrhythmogenic right ventricular dysplasia: a 16-year experience". Current Cardiology Reports. 2 (6): 498–506. doi:10.1007/s11886-000-0034-1. PMID 11203287. S2CID 31406061.

ucl.ac.uk

discovery.ucl.ac.uk

Protonotarios A, Brodehl A, Asimaki A, Jager J, Quinn E, Stanasiuk C, et al. (June 2021). "The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy". The Canadian Journal of Cardiology. 37 (6): 857–866. doi:10.1016/j.cjca.2020.11.017. PMID 33290826. S2CID 228078648.

web.archive.org

Jardy A. "Crew midfielder Kirk Urso, 22, dies after being rushed to hospital from bar". The Columbus Dispatch. The Dispatch Printing Company. Archived from the original on 17 October 2012. Retrieved 21 September 2012.
Jardy A. "Coroner: Crew's Urso died of a preexisting heart condition". The Columbus Dispatch. The Dispatch Printing Company. Archived from the original on 24 September 2012. Retrieved 21 September 2012.
"Cause of Death". Cardiac Inherited Disease Group. Archived from the original on 2006-08-18. Retrieved 2006-10-31.

youtube.com

The life and career of Jordan Boyd | NHL Home Team Heroes, 13 October 2019, retrieved 2019-10-14