160 related articles for article (PubMed ID: 25693453)
1. Identification of arrhythmogenic right ventricular cardiomyopathy-causing gene mutations in young sudden unexpected death autopsy cases.
Sato T; Nishio H; Suzuki K
J Forensic Sci; 2015 Mar; 60(2):457-61. PubMed ID: 25693453
[TBL] [Abstract][Full Text] [Related]
2. Unique genetic background and outcome of non-Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Wada Y; Ohno S; Aiba T; Horie M
Mol Genet Genomic Med; 2017 Nov; 5(6):639-651. PubMed ID: 29178656
[TBL] [Abstract][Full Text] [Related]
3. Mutations of desmoglein-2 in sudden death from arrhythmogenic right ventricular cardiomyopathy and sudden unexplained death.
Zhang M; Xue A; Shen Y; Oliveira JB; Li L; Zhao Z; Burke A
Forensic Sci Int; 2015 Oct; 255():85-8. PubMed ID: 26296472
[TBL] [Abstract][Full Text] [Related]
4. Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy.
Lahtinen AM; Lehtonen E; Marjamaa A; Kaartinen M; Heliö T; Porthan K; Oikarinen L; Toivonen L; Swan H; Jula A; Peltonen L; Palotie A; Salomaa V; Kontula K
Heart Rhythm; 2011 Aug; 8(8):1214-21. PubMed ID: 21397041
[TBL] [Abstract][Full Text] [Related]
5. Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy.
Pilichou K; Nava A; Basso C; Beffagna G; Bauce B; Lorenzon A; Frigo G; Vettori A; Valente M; Towbin J; Thiene G; Danieli GA; Rampazzo A
Circulation; 2006 Mar; 113(9):1171-9. PubMed ID: 16505173
[TBL] [Abstract][Full Text] [Related]
6. High risk of heart failure associated with desmoglein-2 mutations compared to plakophilin-2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Hermida A; Fressart V; Hidden-Lucet F; Donal E; Probst V; Deharo JC; Chevalier P; Klug D; Mansencal N; Delacretaz E; Cosnay P; Scanu P; Extramiana F; Keller DI; Rouanet S; Charron P; Gandjbakhch E
Eur J Heart Fail; 2019 Jun; 21(6):792-800. PubMed ID: 30790397
[TBL] [Abstract][Full Text] [Related]
7. Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy.
Rigato I; Bauce B; Rampazzo A; Zorzi A; Pilichou K; Mazzotti E; Migliore F; Marra MP; Lorenzon A; De Bortoli M; Calore M; Nava A; Daliento L; Gregori D; Iliceto S; Thiene G; Basso C; Corrado D
Circ Cardiovasc Genet; 2013 Dec; 6(6):533-42. PubMed ID: 24070718
[TBL] [Abstract][Full Text] [Related]
8. Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Bauce B; Nava A; Beffagna G; Basso C; Lorenzon A; Smaniotto G; De Bortoli M; Rigato I; Mazzotti E; Steriotis A; Marra MP; Towbin JA; Thiene G; Danieli GA; Rampazzo A
Heart Rhythm; 2010 Jan; 7(1):22-9. PubMed ID: 20129281
[TBL] [Abstract][Full Text] [Related]
9. Age-dependent clinical and genetic characteristics in Japanese patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Ohno S; Nagaoka I; Fukuyama M; Kimura H; Itoh H; Makiyama T; Shimizu A; Horie M
Circ J; 2013; 77(6):1534-42. PubMed ID: 23514727
[TBL] [Abstract][Full Text] [Related]
10. Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression.
Sen-Chowdhry S; Syrris P; Ward D; Asimaki A; Sevdalis E; McKenna WJ
Circulation; 2007 Apr; 115(13):1710-20. PubMed ID: 17372169
[TBL] [Abstract][Full Text] [Related]
11. PKP2 mutations in sudden death from arrhythmogenic right ventricular cardiomyopathy (ARVC) and sudden unexpected death with negative autopsy (SUDNA).
Zhang M; Tavora F; Oliveira JB; Li L; Franco M; Fowler D; Zhao Z; Burke A
Circ J; 2012; 76(1):189-94. PubMed ID: 22019812
[TBL] [Abstract][Full Text] [Related]
12. Screening of pathogenic genes in Chinese patients with arrhythmogenic right ventricular cardiomyopathy.
Bao JR; Wang JZ; Yao Y; Wang YL; Fan XH; Sun K; Zhang S; Hui RT; Song L
Chin Med J (Engl); 2013 Nov; 126(22):4238-41. PubMed ID: 24238504
[TBL] [Abstract][Full Text] [Related]
13. Sudden death during exercise in a juvenile with arrhythmogenic right ventricular cardiomyopathy and desmoglein-2 gene substitution: a case report.
Sato T; Nishio H; Suzuki K
Leg Med (Tokyo); 2011 Nov; 13(6):298-300. PubMed ID: 22000064
[TBL] [Abstract][Full Text] [Related]
14. Comprehensive analysis of desmosomal gene mutations in Han Chinese patients with arrhythmogenic right ventricular cardiomyopathy.
Zhou X; Chen M; Song H; Wang B; Chen H; Wang J; Wang W; Feng S; Zhang F; Ju W; Li M; Gu K; Cao K; Wang DW; Yang B
Eur J Med Genet; 2015 Apr; 58(4):258-65. PubMed ID: 25765472
[TBL] [Abstract][Full Text] [Related]
15. Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.
Fressart V; Duthoit G; Donal E; Probst V; Deharo JC; Chevalier P; Klug D; Dubourg O; Delacretaz E; Cosnay P; Scanu P; Extramiana F; Keller D; Hidden-Lucet F; Simon F; Bessirard V; Roux-Buisson N; Hebert JL; Azarine A; Casset-Senon D; Rouzet F; Lecarpentier Y; Fontaine G; Coirault C; Frank R; Hainque B; Charron P
Europace; 2010 Jun; 12(6):861-8. PubMed ID: 20400443
[TBL] [Abstract][Full Text] [Related]
16. Correlation of ventricular arrhythmias with genotype in arrhythmogenic right ventricular cardiomyopathy.
Bao J; Wang J; Yao Y; Wang Y; Fan X; Sun K; He DS; Marcus FI; Zhang S; Hui R; Song L
Circ Cardiovasc Genet; 2013 Dec; 6(6):552-6. PubMed ID: 24125834
[TBL] [Abstract][Full Text] [Related]
17. Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers.
Bhonsale A; Groeneweg JA; James CA; Dooijes D; Tichnell C; Jongbloed JD; Murray B; te Riele AS; van den Berg MP; Bikker H; Atsma DE; de Groot NM; Houweling AC; van der Heijden JF; Russell SD; Doevendans PA; van Veen TA; Tandri H; Wilde AA; Judge DP; van Tintelen JP; Calkins H; Hauer RN
Eur Heart J; 2015 Apr; 36(14):847-55. PubMed ID: 25616645
[TBL] [Abstract][Full Text] [Related]
18. Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.
Zorzi A; Rigato I; Pilichou K; Perazzolo Marra M; Migliore F; Mazzotti E; Gregori D; Thiene G; Daliento L; Iliceto S; Rampazzo A; Basso C; Bauce B; Corrado D
Europace; 2016 Jul; 18(7):1086-94. PubMed ID: 26138720
[TBL] [Abstract][Full Text] [Related]
19. Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells.
Asimaki A; Protonotarios A; James CA; Chelko SP; Tichnell C; Murray B; Tsatsopoulou A; Anastasakis A; te Riele A; Kléber AG; Judge DP; Calkins H; Saffitz JE
Circ Arrhythm Electrophysiol; 2016 Feb; 9(2):e003688. PubMed ID: 26850880
[TBL] [Abstract][Full Text] [Related]
20. Frequency of genetic variants associated with arrhythmogenic right ventricular cardiomyopathy in the genome aggregation database.
Hall CL; Sutanto H; Dalageorgou C; McKenna WJ; Syrris P; Futema M
Eur J Hum Genet; 2018 Sep; 26(9):1312-1318. PubMed ID: 29802319
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
